bims-imicid Biomed News
on Immunometabolism of infection, cancer and immune-mediated disease
Issue of 2026–08–02
fifty papers selected by
Dylan Gerard Ryan, Trinity College Dublin



  1. Elife. 2026 Jul 27. pii: RP97759. [Epub ahead of print]13
      TNF has a dual effect in Plasmodium infection, bolstering the host's immune defense while also inducing sickness behavior. Here, we confirm that TNF signaling hampers physical activity, food intake, and energy expenditure while enhancing glucose uptake by the liver and spleen, as well as controlling parasitemia in Plasmodium chabaudi (Pc)-infected mice. We also report that TNF is required for expression of inducible nitric oxide synthase (iNOS), stabilization of hypoxia-inducible factor 1α (HIF-1α), expression of glucose transporter GLUT1, and enhanced glycolysis in monocytic cells from Pc-infected mice. Importantly, Pc-infected Nos2-/-, TNFR1 cKO, and HIF-1a cKO mice show impaired release of TNF and glycolysis in monocytes, along with increased parasitemia and disease tolerance. Altogether, our results indicate that TNF-iNOS-HIF-1α-induced glycolysis in monocytes plays a critical role in host defense and sickness behavior in Pc-infected mice.
    Keywords:  TNF; immunology; immunometabolism; infectious disease; inflammation; malaria; microbiology; mouse; p. chabaudi
    DOI:  https://doi.org/10.7554/eLife.97759
  2. mBio. 2026 Jul 27. e0113326
      Correlates that predict protection against intracellular pathogens, including the highly pathogenic bacterium Francisella, are of interest to evaluate novel candidate vaccines and to facilitate clinical trials. We have previously established an in vitro co-culture assay that measures the control of intramacrophage bacterial replication by immune T cells and serves as a functional correlate. Moreover, this assay is a tool to identify additional molecular correlates of protection and to better understand protective T cell responses against Francisella. To study the role of metabolic shifts in protective T cell responses, we used co-cultures to profile the metabolic activities of macrophages and lymphocytes from mice vaccinated with F. tularensis Live Vaccine Strain (LVS). Previous studies indicated that LVS infection of macrophages dysregulates macrophage metabolism and limits glycolysis. Here, we show that co-cultures of LVS-infected macrophages with LVS-primed lymphocytes, which controlled intramacrophage bacterial growth, exhibited more glycolysis than co-cultures containing naïve cells. Further, LVS-primed lymphocytes exhibited a significant loss of respiratory capacity over time, consistent with a transition to an effector T cell state. Gene expression analyses of splenic T cells recovered from co-cultures revealed a set of metabolic genes that were not only upregulated in glycolytic LVS-primed T cells but could also be detected in total primed splenocytes and peripheral blood lymphocytes. Taken together, we find that LVS-primed effector T cells override bacterial-induced metabolic dysregulation in macrophages to control bacterial infection. These results support future studies exploring the use of metabolic intermediates as potential correlates of protection.IMPORTANCECurrently, there are no licensed vaccines against the deadly bacterium Francisella tularensis, which causes the disease called tularemia in people and in many animals. F. tularensis is also a potential bioterrorism agent. In this study, we showed that metabolic activity measurements of cells from mice immunized with a candidate tularemia vaccine correlated well with protection against disease. These results suggest a new approach to developing lab tests that can predict successful vaccination before undertaking a clinical trial.
    Keywords:  Francisella tularensis; T-cell immunity; glycolysis; immune correlates; immunometabolism; intracellular bacteria; live vaccine strain; mitochondrial metabolism; vaccines
    DOI:  https://doi.org/10.1128/mbio.01133-26
  3. Front Oncol. 2026 ;16 1849888
      Glioblastoma (GBM) remains the most lethal primary brain tumour, with median overall survival of 14 to 16 months despite maximal safe surgical resection, concurrent chemoradiotherapy, and adjuvant temozolomide. Treatment failure is driven in large part by a profoundly immunosuppressive tumour microenvironment (TME) in which metabolic competition between GBM cells, bone marrow-derived immunosuppressive myeloid cells, and cytotoxic T lymphocytes determines cellular dominance. This review frames the GBM TME through the lens of metabolic cell competition: a process by which differential metabolic fitness, mediated principally through glucose and glutamine consumption, establishes a suppressive hierarchy that forecloses effective anti-tumour immunity. Aerobic glycolysis in GBM cells produces lactate, which polarises tumour-associated macrophages toward immunosuppressive phenotypes via GPR81/HIF-1alpha signalling and directly impairs T cell effector function through extracellular acidification and competition for monocarboxylate transporter capacity. GBM cells and immunosuppressive myeloid cells cannot sustain their proliferative and immunosuppressive programmes without glucose and glutamine; cytotoxic memory T cells, whose effector functions are energetically but not biosynthetically demanding, retain the capacity to function through fatty acid oxidation when these substrates are restricted. Disrupting glucose and glutamine metabolism through glutamine antagonism (DON and prodrugs JHU083/JHU395), dichloroacetate (DCA)-mediated PDK inhibition, intravenous pharmacological ascorbate-mediated GAPDH inactivation and HIF-1alpha destabilisation, systemic glucose restriction (SGLT2 inhibitors), sodium phenylbutyrate-mediated glutamine depletion, and monocarboxylate transporter inhibition can invert this competitive hierarchy, reprogramming the immunosuppressive myeloid compartment while preserving T cell fitness; mebendazole is additionally reviewed as a multi-target anti-parasitic repurposing candidate with demonstrated GBM preclinical survival benefit. Pharmacological ketosis elevates beta-hydroxybutyrate, an endogenous HDAC inhibitor that further augments T cell effector function through NLRP3 inflammasome suppression. The mechanistic and clinical evidence for each intervention is reviewed, metabolic engineering strategies for increasing T cell competitive fitness are described, and principal research gaps are identified. GBM cells and immunosuppressive myeloid cells are proposed to constitute a substrate-dependent competitive coalition whose simultaneous disruption is the central therapeutic proposition reviewed. Evidence is synthesised from in vitro metabolic competition experiments, immune-competent murine GBM models, mechanistic pharmacology studies, and early-phase clinical pharmacodynamic data in human GBM.
    Keywords:  fatty acid oxidation; glioblastoma; glutamine metabolism; glycolysis; metabolic cell competition; pharmacological immunometabolism; tumour microenvironment; tumour-associated macrophages
    DOI:  https://doi.org/10.3389/fonc.2026.1849888
  4. Immunology. 2026 Jul 27.
      Integration of intracellular signalling and metabolic reprogramming is critical for macrophage polarisation and the induction of pro- or anti-inflammatory responses. However, the molecular switches that govern these processes remain incompletely defined. While 4-1BB ligand (4-1BBL), a member of the TNF superfamily, is known to promote sustained pro-inflammatory responses in macrophages, its role in anti-inflammatory macrophage responses has not been fully elucidated. This study identifies that 4-1BBL serves as a negative regulator of anti-inflammatory macrophage polarisation. Genetic deletion or pharmacological inhibition of 4-1BBL significantly enhanced the expression of anti-inflammatory cytokines and markers in mouse macrophages. In IL-4R signalling, 4-1BBL restrained Janus kinase 1 (JAK1) and signal transducer and activator of transcription 6 (STAT6) phosphorylation, thereby modulating transcriptional programmes associated with anti-inflammatory macrophage activation. Consistently, 4-1BBL deficiency elevated mitochondrial oxidative phosphorylation and fatty acid oxidation, accompanied by increased expression of metabolic genes in anti-inflammatory macrophages. Transcriptomic analysis further revealed a shift towards anti-inflammatory and oxidative metabolic gene signatures in IL-4-treated 4-1BBL-deficient macrophages. Importantly, the inhibition of 4-1BBL signalling also augmented anti-inflammatory responses in human monocytes and facilitated the transition from pro-inflammatory to anti-inflammatory phenotypes. Collectively, these findings establish 4-1BBL as a crucial molecular switch that regulates macrophage polarisation by integrating inflammatory signalling with metabolic reprogramming, highlighting 4-1BBL as a potential therapeutic target for promoting inflammation resolution.
    Keywords:  4‐1BB ligand; cell metabolism; inflammation; macrophage
    DOI:  https://doi.org/10.1111/imm.70173
  5. Int J Biol Sci. 2026 ;22(12): 6689-6708
      Emerging evidence has shown that fatty acid metabolism is closely associated with autoreactive T cells in autoimmunity, but its function in Sjögren's syndrome (SS) is still unclear. Here, we identified acyl-CoA synthetase long-chain family member 5 (ACSL5) as a metabolic checkpoint that drives pathogenic T-cell responses in SS. ACSL5 was upregulated in patients with SS and positively correlated with T-cell infiltration and lipid dysregulation. ACSL5-high T cells presented hyperactive effector activity and a proinflammatory phenotype. Metabolic profiling indicated that ACSL5 increased fatty acid uptake and utilization and promoted fatty acid oxidation (FAO) through peroxisome proliferator-activated receptor alpha (PPARα) in T cells, thereby improving mitochondrial respiratory capacity. Mechanistically, ACSL5 facilitated the nuclear translocation of PPARα and subsequent Mitofusin 2 (MFN2) transcription, increasing mitochondrial elongation and the formation of mitochondria‒endoplasmic reticulum contacts (MERCs) to influence the FAO and T-cell response. Disruption of the ACSL5/PPARα/MFN2 axis attenuated effector functions and reduced the longevity of pathogenic effector T cells. Pharmacological inhibition of FAO or ACSL5 decreased inflammatory T-cell infiltration and alleviated salivary gland inflammation. Collectively, these findings reveal an ACSL5-centered metabolic program that sustains pathogenic T-cell responses in SS and suggest ACSL5/FAO as a potential therapeutic target.
    Keywords:  ACSL5; MERCs; Sjögren's syndrome; T cells; T-cell memory; fatty acid oxidation
    DOI:  https://doi.org/10.7150/ijbs.131033
  6. Inflammopharmacology. 2026 Jul 28.
      Multiple sclerosis (MS) has conventionally been considered a prototypical autoimmune disorder. While modern immunotherapies effectively control relapsing conditions, they fail to avert progressive neuroinflammation, neurodegeneration, and remyelination failure. This review offers an evidence-based recontextualization. The pathogenesis of multiple sclerosis is multifactorial, resulting from the interaction of genetic predisposition (especially HLA alleles), environmental factors (particularly Epstein-Barr virus infection), B-cell-mediated autoimmunity, and localized CNS inflammation. In this intricate environment, cellular metabolic dysregulation is a notable factor and potentially adjustable enhancer of disease progression, functioning within the extensive multifactorial pathogenic context, where the bioenergetic programming of immune and neural cells determines inflammatory or protective responses. Proinflammatory Th17 cells and M1 microglia depend on aerobic glycolysis and glutaminolysis regulated by mTOR and HIF-1α, whereas regulatory T cells, M2 microglia, and neurons require fatty acid oxidation and oxidative phosphorylation via AMPK. In multiple sclerosis, glycolysis disrupts metabolic equilibrium, sustaining chronic neuroinflammation and obstructing repair processes. Established multiple sclerosis therapies, dimethyl fumarate and teriflunomide, exhibit direct, previously unrecognized metabolic effects, validating this pathway as therapeutically viable. Emerging strategies intentionally target these vulnerabilities: glutaminase inhibitors to counteract pathogenic Th17 cells, AMPK activators such as metformin to enhance remyelination, mTOR inhibitors to restore immune tolerance, and NAD + precursors to rejuvenate mitochondrial function. Transitioning from broad immunosuppression to specific metabolic reprogramming offers remarkable opportunities for tackling chronic neuroinflammation and correcting remyelination deficits in progressive multiple sclerosis. Immuno-metabolic pharmacology is a promising field; however, its clinical application necessitates stringent validation via meticulously designed trials and dependable biomarkers.
    Keywords:  AMPK; Drug repurposing; Immunometabolism; Multiple Sclerosis; Neuroinflammation; mTOR signaling
    DOI:  https://doi.org/10.1007/s10787-026-02350-y
  7. Immunology. 2026 Jul 26.
      Chronic inflammatory and autoimmune diseases are characterised by dysregulated Th1 and Th17 immune responses, leading to excessive production of proinflammatory cytokines. Shikonin (SK) is a natural anti-inflammatory compound whose therapeutic use is limited by poor solubility and bioavailability. Here, we evaluated SK-loaded hyaluronic acid-zein (HA-Zein) nanogels as a targeted strategy to modulate inflammatory CD4+ T-cell responses in vitro and in vivo. HA-Zein nanogels were designed to preferentially target CD44+ activated/effector T cells, key mediators of inflammation in Th1- or Th17-associated diseases. SK-HA-Zein nanogels preferentially interacted with CD44+ activated CD4+ T cells and reduced IFN-γ production and Th1-associated polarisation while preserving Th17-associated readouts. At higher concentrations, SK enhanced FoxP3/IL-10-associated regulatory features. Metabolomic analysis revealed that SK-HA-Zein nanogels inhibited key metabolic activities of Th1 cells, including glutamine and glucose consumption, thereby reducing overall cellular activity. In an acute in vivo inflammation model, SK-HA-Zein nanogels reduced local IFN-γ levels and inflammatory cell infiltration. These findings support SK-HA-Zein nanogels as a targeted immunometabolic strategy to dampen inflammatory CD4+ T-cell responses and promote regulatory features in chronic inflammatory settings.
    Keywords:  CD44 targeting; Shikonin; Th1 polarisation; immunometabolism; nanogels
    DOI:  https://doi.org/10.1111/imm.70169
  8. bioRxiv. 2026 Jul 24. pii: 2026.07.23.740149. [Epub ahead of print]
      Orthoflaviviruses depend on host metabolic resources to replicate, but how distinct cell types in the central nervous system (CNS) alter their metabolism in response to infection remains incompletely understood. Here, we examined whether the NAD+-dependent deacetylase SIRT1 is engaged during Zika virus (ZIKV) and West Nile virus (WNV) infection and whether its activity influences infection outcomes. SIRT1 activity increased in astrocytes isolated from infected mouse brains and in infected primary human astrocytes, but not in neurons or CNS myeloid cells. In astrocytes, infection induced transcriptomic, metabolomic, and functional changes consistent with SIRT1 activation, enhanced NAD+ salvage, and enhanced oxidative metabolism. Pharmacologic inhibition of SIRT1 or NAD+ salvage reduced ZIKV replication in astrocytes, whereas SIRT1 activation or supplementation with an NAD+ precursor increased replication. In mice, SIRT1 inhibition or nicotinamide (NAM) treatment reduced viral burden and mortality following ZIKV and WNV infection, while SIRT1 activation worsened disease. Together, these findings identify NAD+/SIRT1 as key regulators of cellular metabolism in infected astrocytes and support a role for this pathway in promoting orthoflavivirus replication and pathogenesis.
    DOI:  https://doi.org/10.64898/2026.07.23.740149
  9. Cell Rep Methods. 2026 Jul 30. pii: S2667-2375(26)00238-9. [Epub ahead of print] 101537
      Most established bioenergetic assays lack single-cell resolution and may mask metabolic heterogeneity. The main flow-cytometry-based approach for bioenergetic analysis infers energetic state from protein synthesis, although translation can become uncoupled from ATP availability under physiologic and pathologic conditions. Here, we evaluated ATP-Red as a flow-cytometry-compatible readout of energetic state at single-cell resolution. We benchmarked ATP-Red against orthogonal approaches, including colorimetric ATP quantification, the ATP/ADP biosensor PercevalHR, and extracellular flux analysis, across ATPase inhibition, glycolytic and oxidative blockade, mitochondrial dysfunction, and immune activation. Across these settings, ATP-Red tracked biologically meaningful energetic changes as a relative ATP-linked fluorescence readout. When combined with immunophenotyping, ATP-Red also captured bioenergetic heterogeneity and pathway use in T cells following activation and during influenza virus infection. These findings support ATP-Red as a practical and scalable approach for single-cell bioenergetic phenotyping.
    Keywords:  ATP-Red; CP: metabolism; flow cytometry; glycolysis; immunometabolism; metabolic phenotyping; mitochondrial dysfunction; oxidative phosphorylation; single-cell bioenergetics
    DOI:  https://doi.org/10.1016/j.crmeth.2026.101537
  10. Immunology. 2026 Jul 26.
      Methionine is an essential amino acid critical for T cell activation. While methionine restriction (MR) combined with immune checkpoint blockade has been shown to enhance T cell function, the impact of methionine on adoptive T cell therapies remains unknown. Here, we examined the functionality of T cells under MR and pharmaceutical inhibition of the methionine cycle (MAT2Ai), using primary T cells and a murine adoptive T cell therapy model. In vitro, transient MR or MAT2Ai treatment increased interferon gamma (IFNγ) expression in CD8+ T cells, whereas sustained MR led to the upregulation of T cell exhaustion-associated markers. Mechanistically, transient MR suppressed the polyamine synthesis pathway, and supplementation with polyamines reversed MR-induced IFNγ expression. Genetic ablation of S-adenosylmethionine decarboxylase, an enzyme involved in the polyamine synthesis pathway, recapitulated the effect of MR, indicating that transient MR enhances T cell function by inhibiting polyamine synthesis. Despite this, transient MR treatment of ovalbumin (OVA)-specific (OT-I) CD8+ T cells prior to adoptive transfer did not improve antitumour efficacy against EG7-OVA tumours in vivo. In contrast, sustained dietary MR accelerated EG7-OVA tumour growth in mice treated with OT-I T cells, demonstrating that methionine availability is essential for the activity of donor T cells. Importantly, sustained dietary MR promoted terminally exhausted phenotype in tumour-infiltrating donor CD8+ T cells, but not in host T cells. These findings suggest that enhancing methionine availability in the tumour microenvironment may improve the efficacy of adoptive T cell therapies.
    Keywords:  T cell; adoptive cell therapy; cancer immunology; immunometabolism
    DOI:  https://doi.org/10.1111/imm.70177
  11. Front Immunol. 2026 ;17 1793796
      Macrophages play a pivotal regulatory role in inflammation, tissue repair, and fibrosis through their dynamic changes in phenotype and function. The tissue microenvironment following injury induces alterations in key metabolic enzymes, signaling pathways, and metabolites within macrophages, thereby driving shifts in their phenotype and function. Early in acute injury, macrophages primarily rely on glycolysis and the pentose phosphate pathway, transitioning to a pro-inflammatory phenotype. Persistent activation of pro-inflammatory macrophages can lead to tissue damage. As the metabolic microenvironment evolves, the expression of glycolysis-related genes is suppressed, while the expression of genes related to oxidative phosphorylation and the tricarboxylic acid cycle is upregulated, promoting the gradual shift of macrophages toward an anti-inflammatory phenotype. This process plays a crucial role in tissue repair and remodeling. However, sustained activation of anti-inflammatory macrophages may contribute to the development of fibrosis. Therefore, metabolic reprogramming of macrophages presents a novel potential therapeutic target for intervening in inflammatory injury and stromal fibrosis. The high plasticity of macrophages is essential for tissue repair and regeneration, as they regulate inflammation, promote angiogenesis, and facilitate extracellular matrix remodeling, thereby restoring tissue homeostasis. This capability holds promise for the treatment of various conditions, including chronic wounds, fibrotic diseases, and inflammatory disorders.
    Keywords:  chronic tissue injury; inflammation; macrophage; metabolic reprogramming; tissue repair
    DOI:  https://doi.org/10.3389/fimmu.2026.1793796
  12. Cell Rep. 2026 Jul 29. pii: S2211-1247(26)00827-2. [Epub ahead of print]45(8): 117749
      Depression is linked to microglial activation, but the precise triggers and downstream pathways remain elusive. Through single-cell RNA sequencing of human blood samples, we find upregulation of the CCL5-CCR5 axis in patients with major depressive disorder. Using a chronic social defeat stress mouse model, we show that CCR5 is specifically elevated in activated hippocampal microglia. Microglia-specific deletion of CCR5 alleviates depressive-like behaviors and prevents microglial activation. Mechanistically, CCR5 binding to VHL stabilizes HIF-1α, redirecting microglial metabolism toward aerobic glycolysis. This metabolic shift results in lactate accumulation, which drives histone H4 lysine 12 lactylation (H4K12la). Genome-wide profiling reveals that H4K12la enrichment at complement gene promoters facilitates their transcription, ultimately leading to excessive microglial engulfment of neuronal spines and synaptic loss. Importantly, either inhibiting glycolysis or exogenous lactate supplementation can respectively rescue or mimic the pathological synaptic pruning and depressive-like behaviors. Our findings indicate a CCR5-driven immune-metabolic-transcriptional axis in microglia that underlies synaptic deficits in depressive-like behaviors, offering potential targets for therapeutic intervention.
    Keywords:  CCR5; CP: neuroscience; depression; histone lactylation; metabolic reprogramming; metabolism; microglia; synaptic pruning
    DOI:  https://doi.org/10.1016/j.celrep.2026.117749
  13. Front Immunol. 2026 ;17 1867162
      One-carbon metabolism has emerged as a critical interface between tumor metabolic adaptation and antitumor immunity. Beyond its canonical role in nucleotide biosynthesis and redox balance, this metabolic network regulates methyl-donor availability, epigenetic programming, and immune-cell state transitions within the tumor microenvironment. Recent studies show that tumor cells can outcompete T cells for methionine, thereby depleting intracellular S-adenosylmethionine, impairing histone methylation, and driving effector dysfunction or exhaustion. At the same time, tumor-intrinsic one-carbon enzymes such as MTHFD2 actively promote immune escape through PD-L1 upregulation and suppression of innate immune sensing. Serine-related pathways further shape the immune landscape in a context-dependent manner, supporting either immunosuppressive cell accumulation or enhanced tumor immunogenicity depending on the cellular compartment and metabolic state. Importantly, one-carbon metabolism also represents a therapeutic opportunity. Strategies including methionine restriction, formate supplementation, serine-pathway targeting, and methyl-donor modulation have shown potential to enhance antitumor immunity and improve responses to immune checkpoint blockade. However, because one-carbon metabolism is required by both tumor cells and immune cells, effective intervention will require careful attention to cell-type specificity, metabolic context, and therapeutic timing. In this review, we discuss how one-carbon metabolism governs T-cell fitness, epigenetic regulation, and the broader tumor immune ecosystem, and we highlight emerging translational strategies for exploiting this pathway in cancer immunotherapy.
    Keywords:  T-cell fitness; cancer immunity; epigenetic programming; immunometabolism; one-carbon metabolism
    DOI:  https://doi.org/10.3389/fimmu.2026.1867162
  14. Diabetes Obes Metab. 2026 Jul 30.
       CONTEXT: Islet-resident macrophages (IRMs) have emerged as important regulators of pancreatic islet biology, operating at the intersection of metabolism and immunity. Beyond their classical roles as immune sentinels, accumulating evidence indicates that IRMs dynamically integrate β-cell activity, environmental cues, and metabolic stress, thereby coordinating islet homeostasis, adaptive remodelling, and disease progression. However, their context-dependent functions and therapeutic potential remain incompletely understood.
    EVIDENCE ACQUISITION: This review summarizes current evidence regarding IRM origins, phenotype, metabolic plasticity, and bidirectional crosstalk with β cells in health, type 1 diabetes, and type 2 diabetes. We further review emerging therapeutic concepts targeting macrophage metabolism, intercellular communication, and organelle function, while discussing current challenges in translating findings from murine IRMs to human disease.
    EVIDENCE SYNTHESIS: Under physiological conditions, IRMs maintain islet integrity through surveillance, efferocytosis, trophic signalling, redox control, and maintenance of intercellular communication within the islet niche. In diabetes, chronic glucolipotoxicity, autoimmunity, oxidative stress, and amyloid-associated injury can redirect these homeostatic programs toward maladaptive inflammatory states that impair insulin secretion and accelerate β-cell loss. Collectively, these findings support a unified framework in which IRMs act as immunometabolic hubs integrating local and systemic signals to determine β-cell fate.
    CONCLUSIONS: IRMs represent central immunometabolic hubs that orchestrate β-cell fate during health and diabetes. Emerging therapeutic strategies targeting macrophage metabolism, intercellular communication, and organelle function may help prioritize future mechanistic studies and guide safer macrophage-centered interventions for diabetes.
    Keywords:  diabetes; extracellular vesicles; immunometabolism; islet inflammation; islet‐resident macrophages; β‐cells
    DOI:  https://doi.org/10.1111/dom.71154
  15. Cell Rep. 2026 Jul 25. pii: S2211-1247(26)00808-9. [Epub ahead of print]45(8): 117730
      Host-microbiota metabolic interactions critically regulate nicotinamide adenine dinucleotide (NAD+) homeostasis, and their disruption is increasingly linked to chronic diseases, including inflammatory bowel disease (IBD). However, it remains unclear whether NAD+ dysregulation in IBD arises from impaired production, enhanced consumption, or both. Using multi-omics approaches and stable isotope-labeled NAD+ precursors administered via intravenous infusion in a murine model of dextran sulfate sodium (DSS)-induced colitis, we mapped tissue- and lumen-specific NAD+ metabolism under inflammatory stress. Our results reveal tissue-specific rewiring of NAD+ metabolism, with increased flux through the salvage pathway compensating for reduced de novo NAD+ synthesis from tryptophan. In parallel, microbial de novo NAD+ production was elevated, highlighting a cooperative host-microbiota response to inflammatory stress. These findings demonstrate differential regulation of NAD+ biosynthesis during acute colitis and underscore the dynamic interplay between host and microbial metabolism in maintaining NAD+ homeostasis under inflammatory conditions.
    Keywords:  CP: metabolism; CP: microbiology; DSS colitis; IBD; NAD(+); gut microbiota; host-microbiome interactions; kynurenine pathway; metabolomics; nicotinamide; stable isotope tracing; tryptophan
    DOI:  https://doi.org/10.1016/j.celrep.2026.117730
  16. PLoS Pathog. 2026 Jul 30. 22(7): e1013860
      Infection rates involving bacterial and viral pathogens have increased precipitously after the COVID-19 pandemic, though underlying causes remain elusive. Potential causes ranging from increased hospitalizations during the pandemic or greater use of antibiotics have been proposed, but precisely why rates remain high today remains unknown. Here, we demonstrate that decreased mitochondrial function in antigen-specific T cells post-COVID may contribute to higher infection susceptibility by metabolically immobilizing T cell responses. Using donor-matched peripheral blood samples from 31 COVID-naïve individuals who subsequently contracted COVID-19, we tracked how influenza A (IAV), Staphylococcus aureus (SA), and Varicella-zoster virus (VZV)-stimulated T cell responses were impacted by SARS-CoV-2 infection. Post-COVID CD4 memory T cells exhibited decreased activation- and increased mitochondrial redox-related gene expression. Despite this, mitochondrial flux and reactive oxygen species production were functionally limited in post-COVID antigen-specific T cells after stimulation with IAV, SA, and VZV. Post-COVID plasma was depleted in carnitine and TCA cycle species important for activating fatty acid oxidation, and this correlated with a disordered relationship between memory T cell mobilization of glycolysis, fatty acid metabolism, and oxidative phosphorylation pathways. Metabolic perturbations ultimately resulted in diminished use of catabolic, energy-generating pathways including glycolysis and fatty acid oxidation in antigen-specific T cells. Activating mitochondrial function with metformin and ubiquinol partially rescued the post-COVID decline in T cell catabolism. Collectively, these findings indicate that COVID-19 infection may inhibit T cell metabolism upon exposure to commonly encountered pathogens, which can be partly corrected with commonly available medications that activate mitochondrial metabolism. Our findings may have significant implications for the clinical care of immunologically vulnerable populations in the post-pandemic era.
    DOI:  https://doi.org/10.1371/journal.ppat.1013860
  17. Int Immunopharmacol. 2026 Jul 26. pii: S1567-5769(26)01017-9. [Epub ahead of print]187 117171
      Carboxyamidotriazole (CAI), an inhibitor of mitochondrial complex I, demonstrates anti-inflammatory and anti-tumor properties. While effective against colitis, its potential link to macrophage metabolism in colitis and colitis-associated colorectal cancer (CAC) remained unexplored. This study investigates the role of CAI and its association with macrophage metabolic states in these conditions. In the acute phase, CAI alleviates dextran sulfate sodium (DSS)-induced colitis, which is accompanied by suppressed IL-1β expression in pro-inflammatory macrophages. As a mitochondrial respiratory chain inhibitor, CAI treatment is associated with metabolic alterations characterized by accumulated α-ketoglutarate (α-KG) and decreased succinate and acetyl-CoA. This rewiring correlates with reduced hypoxia-inducible factor 1-alpha (HIF-1α) and decreased H3K27 acetylation (H3K27ac) at the Il1b locus. In the azoxymethane (AOM)/DSS model of CAC, we observed CD86+CD206+ mixed-phenotype macrophages during chronic inflammation. In CD206+ macrophages, CAI treatment is linked to the inhibition of oxidative phosphorylation (OXPHOS) and fatty acid β-oxidation (FAO), concomitant with reactive oxygen species (ROS) reduction and impaired Stat6 phosphorylation. Concurrently, accumulated fatty acids are associated with increased PPARγ signaling. This coordinated modulation of Stat6 and PPARγ pathways correlates with sustained anti-inflammatory effects, as well as with reduced expression of pro-fibrotic and pro-angiogenic mediators. Our findings position CAI's effects in colitis and CAC alongside dynamic changes in macrophage metabolism. This work provides new insights into targeting metabolic pathways in inflammatory carcinogenesis.
    Keywords:  Carboxyamidotriazole; Colitis; Colitis-associated carcinogenesis; Macrophage; Metabolic reprogramming
    DOI:  https://doi.org/10.1016/j.intimp.2026.117171
  18. Cell Rep. 2026 Jul 27. pii: S2211-1247(26)00814-4. [Epub ahead of print]45(8): 117736
      Host-gut microbiota metabolic interactions are implicated in the pathogenesis of ulcerative colitis (UC), but the underlying mechanisms of certain metabolites remain ambiguous. Here, we revealed an impaired bile acid homeostasis in UC with a significant deficiency of hyodeoxycholic acid (HDCA), which was inversely correlated with the severity of UC. Ruminococcus callidus was linked to altered HDCA generation, and colonization of R. callidus increased HDCA concentrations via bile salt hydrolase. Single-cell RNA sequencing (ScRNA-seq) indicated that HDCA reshaped the intestinal macrophage landscape by enriching a metabolically rewired Mrc1+ macrophage subpopulation with immunosuppressive features. Mechanistically, HDCA enhanced PPARγ-mediated fatty acid metabolism reprogramming to alleviate inflammation, which was blunted in myeloid PPARγ-deficient mice. HDCA triggered fatty acid oxidation to promote ATP citrate lyase-dependent histone acetylation, supporting epigenetics-mediated gene regulation and the phenotypic modification of macrophages. These findings uncover a unique mechanism of gut microbiota-derived HDCA regulating metabolism, providing therapeutic potential for UC.
    Keywords:  CP: immunology; CP: metabolism; fatty acid oxidation; histone acetylation; hyodeoxycholic acid; peroxisome proliferator-activated receptor γ; ulcerative colitis
    DOI:  https://doi.org/10.1016/j.celrep.2026.117736
  19. Adv Sci (Weinh). 2026 Jul 31. e23390
      Metabolic reprogramming toward aerobic glycolysis is increasingly recognized as a key mechanism in the pathogenesis of psoriasis, but the underlying regulatory mechanisms remain unclear. Here, we identify Toll-interacting protein (TOLLIP) as a critical regulator of psoriasis pathogenesis through its modulation of glycolytic metabolism. We found that TOLLIP is significantly upregulated in psoriatic lesions, and its genetic deletion in mice exacerbated disease severity in imiquimod (IMQ)-induced psoriasis models. Mechanistically, TOLLIP interacts with the rate-limiting glycolytic enzyme pyruvate kinase M2 (PKM2) via its coupling of ubiquitin to ER degradation (CUE) domain (179-274 aa), inhibits PKM2's metabolic enzyme activity and attenuates aerobic glycolysis, thereby mitigating keratinocyte hyperproliferation and inflammation. Therapeutic delivery of Tollip or Tollip (179-274 aa) via adeno-associated virus (AAV) vectors ameliorated psoriasis progression in mice. Our findings establish the TOLLIP-PKM2-glycolysis axis as a key mechanism linking metabolic reprogramming to psoriasis pathogenesis, and propose TOLLIP as a promising therapeutic target.
    Keywords:  CUE; Glycolysis; PKM2; Psoriasis; TOLLIP
    DOI:  https://doi.org/10.1002/advs.202523390
  20. Proc Natl Acad Sci U S A. 2026 Aug 04. 123(31): e2600260123
      Vitamin D deficiency is associated with dysregulated alloimmune responses, but the mechanisms by which its active metabolite calcitriol shapes innate lymphoid cell (ILC) development and function remain incompletely understood. Here, we elucidate how calcitriol directs the differentiation of bone marrow (BM) ILC progenitors (ILCPs) into anti-inflammatory ILC3s with therapeutic potential in alloimmune diseases. Using murine vitamin D models, integrated omics, 13C-glucose tracing, humanized mouse models, and clinical samples, we show that calcitriol, through the vitamin D receptor (VDR), selectively promotes the expansion and differentiation of BM ILCPs into IL-10+IL-22+ ILC3s that exert tissue-protective effects in the intestine. Calcitriol-primed BM ILCP cell therapy attenuates intestinal inflammation in an alloimmune setting. Mechanistically, a VDR-SYK axis triggers nuclear translocation of pyruvate kinase M2 (PKM2). Nuclear PKM2 phosphorylates STAT3 at Tyr705, forming a dimerization complex with c-JUN that drives Il10 transcription. Simultaneously, cytosolic PKM2 channels pyruvate into pyruvate carboxylase-mediated mitochondrial anaplerosis, sustaining oxidative phosphorylation while suppressing reverse electron transport-driven mitochondrial ROS production. In human studies, patients with severe alloimmune complications exhibit reduced circulating ILCPs and low serum 25(OH)D levels. Calcitriol-treated human CD117+ ILCPs efficiently generate IL-10-producing ILCs in vitro and in humanized models, potently suppressing alloreactive T cell responses. Collectively, calcitriol reprograms BM ILCPs via the VDR-SYK-PKM2 axis to generate dual-cytokine IL-10+IL-22+ ILC3s, establishing PKM2 as a key immunometabolic target and supporting calcitriol-primed ILCP-based cell therapy as a promising approach for alloimmune diseases.
    Keywords:  PKM2; alloimmune responses; cell therapy; immunometabolism; innate lymphoid cells
    DOI:  https://doi.org/10.1073/pnas.2600260123
  21. mBio. 2026 Jul 27. e0149126
      The innate immune response to pathogens often involves metabolic reprogramming, such as disruption of the Krebs cycle, leading to the accumulation of various metabolites that can further influence innate cell responses during infection. Of these, the immunomodulatory metabolite itaconate has been shown to positively or negatively influence lung immune responses, depending on the pathogen. In the current study, we found that mice deficient in aconitate decarboxylase (Acod1-/- mice), the enzyme that produces itaconate from cis-aconitate, cleared the opportunistic mold Aspergillus fumigatus from the lung more effectively than wild-type (WT) control mice. Augmented fungal clearance in Acod1-/- mice correlated with increased type 17 responses, which themselves correlated with higher IL-1β, PGE2, and γδ T cell levels. Intriguingly, we show that alveolar macrophages and neutrophils from naïve Acod1-/- mice kill A. fumigatus more efficiently. Conversely, the addition of exogenous itaconate to alveolar macrophages and neutrophils from naïve WT mice reduced their antifungal capacity. Mechanistically, alveolar macrophages, but not neutrophils, from naïve Acod1-/- mice demonstrated enhanced ROS production when stimulated with A. fumigatus. We further show that mice with macrophage-specific, but not neutrophil-specific, Acod1 deficiency cleared A. fumigatus more effectively. Itaconate deficiency also protected against fungus-induced mortality during corticosteroid-mediated immunosuppression. Finally, itaconate reduced the antifungal activity of human monocyte-derived macrophages. Collectively, these data identify an immune regulatory role for itaconate during A. fumigatus fungal pneumonia and potentially identify a new therapeutic target for enhancing protection against A. fumigatus.IMPORTANCEFungal infections by invasive molds such as Aspergillus fumigatus are leading causes of morbidity and mortality in immunocompromised individuals, such as patients with hematologic malignancies, and recipients of hematopoietic stem cell transplant (HCT), solid organ transplant (SOT), and cellular therapies. A major shift in the increased incidence of these infections is a result of a rapidly expanding global immunocompromised population due to targeted immunotherapies and biologics for the treatment of cancer, combination therapies, cellular therapies, and bispecific and trispecific antibody therapies. The advancement in these immunomodulatory/immunosuppressive therapies is outpacing our understanding of mechanisms that lead to the development of infections such as invasive aspergillosis. Therefore, the continuing evolution of our understanding of protective and immunoregulatory responses would be expected to reveal new mechanisms that govern susceptibility to fungal pneumonia. To this end, in the current report, we show that the TCA cycle intermediate itaconate hinders lung clearance of A. fumigatus via regulating multiple immune mechanisms. Overall, our study uncovers a new mechanism of immune regulation during fungal pneumonia.
    Keywords:  fungal; innate immunity; lung defense
    DOI:  https://doi.org/10.1128/mbio.01491-26
  22. J Immunol. 2026 Jul 10. pii: vkag203. [Epub ahead of print]215(7):
      The innate immune system can detect infection, tissue damage, and other homeostatic disruptions to initiate an immune response, drive inflammation, and promote programmed cell death. While these responses can be beneficial in host defense, aberrant activation of inflammatory, lytic cell death pathways can be pathogenic. Emerging evidence suggests that cellular metabolic disruption can promote inflammatory cell death, but the mechanistic connections between these processes are not well understood, limiting our ability to identify regulatory nodes that can be therapeutically targeted. Here, we found that intracellular levels of the metabolic cofactor nicotinamide adenine dinucleotide (NAD+) were depleted in response to cell death triggers that drive pyroptosis, necroptosis, PANoptosis, and ferroptosis. However, restoring NAD+ inhibited PANoptosis but not the other forms of cell death. Mechanistically, NAD+ restoration reduced the expression of PANoptotic sensors or regulators, including the transcription factor IRF1, a critical factor for innate immune sensor priming in PANoptosis. Our findings thereby suggest that NAD+ depletion is an early cell death signaling event and that restoring NAD+ levels specifically blocks PANoptosis by suppressing priming. Hence, targeting NAD+ metabolism represents a potential therapeutic strategy for infectious and inflammatory diseases associated with dysregulated PANoptosis.
    Keywords:  AIM2; NLRC5; NLRP12; NLRP3; ZBP1
    DOI:  https://doi.org/10.1093/jimmun/vkag203
  23. Allergy. 2026 Jul 31.
       BACKGROUND: Thymic stromal lymphopoietin (TSLP) is a key epithelial alarmin involved in the initiation and maintenance of type 2 inflammatory airway diseases. Although tezepelumab, the first approved anti-TSLP monoclonal antibody, has shown robust clinical efficacy in asthma and CRSwNP, the molecular mechanisms underlying its mode of action remain incompletely defined.
    OBJECTIVE: To determine whether TSLP induces a pathogenic immunometabolic program in human type 2 conventional dendritic cells (cDC2s) and whether tezepelumab can directly reverse this process.
    METHODS: Purified human circulating cDC2s from healthy non-atopic donors were stimulated with TSLP in the presence or absence of tezepelumab. cDC2 phenotype, function, metabolism, and T-cell polarization capacity were assessed. Pathogenic Th2 responses, Treg generation, suppressive function, and metabolic fitness were analyzed.
    RESULTS: TSLP induced a metabolic rewiring in human cDC2s characterized by increased glycolysis and mitochondrial oxidative phosphorylation. This metabolic hyperactivation was associated with the acquisition of a pro-type 2 phenotype and required for the induction of pathogenic T-cell responses. TSLP-activated cDC2s generated pathogenic Th2 cells and FOXP3+ Tregs with impaired suppressive function and an altered metabolic profile. Tezepelumab effectively reversed TSLP-induced metabolic and functional reprogramming in cDC2s, thereby limiting pathogenic Th2 polarization while restoring the functional and metabolic properties of induced Tregs.
    CONCLUSIONS: We identify immunometabolic rewiring as a key mechanism of the TSLP-cDC2 axis and provide mechanistic insight into how tezepelumab reshapes pathogenic adaptive immune responses. These results support upstream epithelial alarmin blockade as a strategy to interfere with early disease-driving immune programs in type 2 inflammatory airway diseases.
    Keywords:  TSLP; asthma; cDC2s; chronic rhinosinusitis with nasal polyps; immunometabolic rewiring; pathogenic Th2 cells; regulatory T cells; tezepelumab
    DOI:  https://doi.org/10.1111/all.70470
  24. Front Immunol. 2026 ;17 1758569
       Introduction: Mitochondrial DNA depletion syndromes (MDS) caused by deoxyguanosine kinase (DGUOK) deficiency are classically attributed to impaired mitochondrial DNA (mtDNA) maintenance. However, many patients develop hepatic steatosis and inflammation despite preserved mtDNA content, suggesting that additional pathogenic mechanisms contribute to disease. DGUOK is a key enzyme in the mitochondrial purine salvage pathway, but its role in coordinating purine metabolism with lipid homeostasis and innate immune signaling remains poorly understood.
    Methods: Acute DGUOK deficiency was induced in human hepatocellular carcinoma (HepG2) hepatocytes by siRNA-mediated knockdown. Mitochondrial integrity was assessed by mtDNA quantification, mitochondrial morphology, and oxidative phosphorylation (OXPHOS) protein expression. Lipid accumulation was evaluated by BODIPY staining, and transcriptomic changes were analyzed by bulk RNA sequencing. Purine imbalance was modeled by treatment of wild-type cells with 2'-deoxyadenosine, followed by assessment of DNA methylation, interferon signaling, and lipid accumulation.
    Results: Acute DGUOK depletion induced a 2.9-fold increase in intracellular lipid droplet accumulation and activation of a type I interferon (IFN) transcriptional program despite preserved mtDNA copy number, mitochondrial morphology, and OXPHOS complex expression. Bulk RNA sequencing revealed induction of human endogenous retroviruses (HERVs) and interferon-stimulated genes (ISGs), together with suppression of lipid metabolic pathways and remodeling of purine-, methionine-, and methylation-associated networks. Consistent with these transcriptional changes, DGUOK-deficient cells exhibited an approximately 40% reduction in global DNA methylation, accompanied by hypomethylation of CpG-rich region within the ISG15 and ISG20 promoters. Perturbation of purine homeostasis with exogenous 2'-deoxyadenosine phenocopied DGUOK deficiency, driving DNA hypomethylation, activation of viral mimicry pathways, and lipid accumulation.a.
    Discussion: These findings demonstrate that acute DGUOK deficiency promotes innate immune activation and metabolic reprogramming through a purine-dependent mechanism that precedes mtDNA depletion and overt mitochondrial dysfunction. By linking disrupted mitochondrial purine salvage to HERV and ISG derepression, interferon signaling, epigenetic remodeling, and steatosis, this study provides a mechanistic framework for the immunometabolic pathology of DGUOK deficiency and identifies mitochondrial purine metabolism as an important regulator of hepatic immune and metabolic homeostasis.
    Keywords:  deoxyguanosine kinase deficiency; hepatic steatosis; human endogenous retroviral elements; immunometabolism; purine metabolism; type I interferon
    DOI:  https://doi.org/10.3389/fimmu.2026.1758569
  25. Front Immunol. 2026 ;17 1894833
      Primary and recurrent brain tumors are aggressive malignancies with high mortality rates and limited treatment options. Glioblastoma (GBM) in particular are largely refractory to immunotherapies despite harboring a significant proportion of immune cells in the tumor microenvironment (TME). Increasing evidence suggests that the immunosuppressive TME in brain tumors is driven by functional and metabolic reprogramming of resident and infiltrating myeloid cells. Here, we examine the determinants of immunometabolic landscape in brain tumors and distinct features of heterogeneous myeloid cell populations. We discuss how interactions between cell types and metabolic programs shape spatial niches. We further dissect the effect of tumor stage, type and therapy in informing metabolic features of the TME. Collectively, this systematic review provides an overview of myeloid cell metabolism in brain tumors and highlights potential opportunities for future studies targeting metabolic states for cancer immunotherapy.
    Keywords:  MDSC; brain metastasis; brain tumor; glioblastoma; immunometabolism; macrophage; metabolism; microglia
    DOI:  https://doi.org/10.3389/fimmu.2026.1894833
  26. bioRxiv. 2026 Jul 16. pii: 2026.07.11.737940. [Epub ahead of print]
      In polymicrobial infections, how the host recognizes and responds to pathogens influences which species will persist to cause chronic infections. The human respiratory tract is a common anatomical site for viral-bacterial co-infections, where primary viral infections predispose to secondary bacterial infections, leading to increased morbidity and mortality. Additionally, co-infections are disproportionately prevalent in people with chronic lung diseases, such as chronic obstructive pulmonary disease and cystic fibrosis. We previously reported that primary viral infections and antiviral interferon (IFN) signaling stimulate Pseudomonas aeruginosa (PA) biofilm formation on airway epithelial cells (AECs). IFN signaling induces aerobic glycolysis in AECs and generates lactate as a cellular byproduct. Given that innate immune systems play an integral role in co-infection dynamics, we investigated the role of host-secreted metabolites (i.e. lactate) on innate immune cell activity during respiratory co-infections. We found that exposure to the apical secretions from IFNβ-treated AECs significantly compromised macrophage antibacterial activity, with the soluble metabolite lactate playing an important role. Macrophages used monocarboxylate transporters and G-protein receptors to transport and/or sense lactate, respectively, and this exposure to lactate diminished their bacterial-killing activity in a time-exposure dependent manner. Lactate exposure particularly reprogrammed macrophage cellular metabolism towards an anti-inflammatory state by increasing oxidative phosphorylation and fatty acid oxidation. Collectively, these findings provide insight into metabolites as complex regulators of trans-kingdom interactions and epithelial-macrophage crosstalk during respiratory co-infections.
    DOI:  https://doi.org/10.64898/2026.07.11.737940
  27. Int Immunopharmacol. 2026 Jul 30. pii: S1567-5769(26)01052-0. [Epub ahead of print]187 117206
      Immunometabolism plays a crucial role in glioma progression, yet the metabolic mechanisms underlying glioma-associated macrophage (GAM)-mediated immunoregulatory remain poorly understood. Here, we analyzed metabolic profiles of gliomas at single-cell resolution and identified aberrant activation of the arachidonic acid (AA) metabolic pathway in GAMs. Further study reveal that AA promoted M2-like polarization of GAMs, and was associated with an immune-dampening tumor microenvironment in murine models. AA-reprogrammed GAMs downregulated MHC-I expression, impairing CD8+ T cell infiltration and harnessing their cytotoxic effector function. Pharmacological inhibition of COX reversed AA-induced GAM reprogramming, delayed tumor progression. These findings suggest that targeting the AA-COX metabolic pathway represents a promising immunotherapeutic strategy for glioma treatment.
    Keywords:  Arachidonic acid; Cyclooxygenase; Glioma; M2 polarization; Tumor-associated macrophage
    DOI:  https://doi.org/10.1016/j.intimp.2026.117206
  28. Front Immunol. 2026 ;17 1842560
      Rheumatoid Arthritis (RA) is a chronic autoimmune disease characterized by persistent synovial inflammation. Recent studies have revealed that immune metabolites, particularly succinate, play a critical role in its pathogenesis. In this review, we systematically analyze the molecular mechanisms underlying succinate accumulation and elucidate how succinate drives inflammatory and immune dysregulation in RA. Hypoxia and inflammation microenvironment drive metabolic alterations, leading to succinate accumulation via three primary mechanisms: 1) succinate retention caused by impaired mitochondrial oxidation, 2) enhanced succinate synthesis through alternative biosynthetic pathways, and 3) increased succinate export into the extracellular space. Accumulated succinate exerts its pathogenic effects through three distinct pathways: (i) binding to its receptor Succinate Receptor 1 (SUCNR1) as an extracellular signaling molecule; (ii) stabilizing Hypoxia-Inducible Factor-1α (HIF-1α) in the intracellular space; and (iii) acting as a key epigenetic modulator. These insights into succinate-mediated pathogenesis provide a rationale for the development of targeted RA therapies, including strategies aimed at SUCNR1, Succinate Dehydrogenase (SDH), and the combination of these metabolic interventions with existing anti-inflammatory treatments.
    Keywords:  HIF-1α; RA; SUCNR1; immunometabolism; succinate
    DOI:  https://doi.org/10.3389/fimmu.2026.1842560
  29. Front Immunol. 2026 ;17 1873494
      The role of saturated fatty acid-induced immunometabolic stress in macrophage dysfunction during metabolic disease remains incompletely understood, particularly the interplay between inflammatory signaling and intracellular lipid handling. We employed a tightly controlled palmitic acid (PA)-based lipotoxicity model in PMA-differentiated U937-derived human macrophage-like cells to investigate how lipid excess reshapes inflammatory responses and to evaluate the modulatory effects of cannabidiol (CBD). PA exposure induced a metabolically stressed yet viable macrophage phenotype, characterized by a broad cytokine remodeling profile. This included induction of classical proinflammatory cytokines such as interleukin (IL)-6, together with activation of inflammasome-associated cytokines IL-1β and IL-18 and additional immunoregulatory mediators, while tumor necrosis factor alpha (TNF-α) contributed to the overall inflammatory profile in a multivariate analysis. These changes were accompanied by a significant, time-dependent storage of intracellular triglycerides (TG) consistent with lipid overload and altered lipid handling. CBD co-treatment did not compromise cell viability but selectively attenuated PA-induced inflammatory response in a cytokine-dependent manner, with the most significant reduction observed at higher concentrations. In parallel, CBD significantly reduced intracellular TG accumulation under lipotoxic conditions. Collectively, these findings define a lipotoxicity-associated macrophage phenotype driven by saturated fatty acids and identify CBD as a context-dependent modulator of immunometabolic inflammation. This work provides a controlled experimental framework to study lipid-driven inflammatory dysfunction and supports the potential of CBD as a targeted strategy to modulate metabolic inflammation without broadly suppressing immune function.
    Keywords:  cannabidiol; immunometabolic; macrophages; palmitic acid; triglycerides
    DOI:  https://doi.org/10.3389/fimmu.2026.1873494
  30. Front Immunol. 2026 ;17 1879634
      Psoriasis (PSO) and atopic dermatitis (AD) are the two most common chronic inflammatory skin diseases in clinical practice. For a long time, they have been classified in pathological immunology under the opposing model of "Th17/IL-17 vs. Th2/IL-4-IL-13." However, over the past decade, with the rise of immunometabolism, our understanding of chronic inflammatory diseases has undergone a significant shift. Metabolic pathways in immune cells are no longer viewed merely as auxiliary systems providing energy, but rather as core regulatory networks that determine cellular differentiation and effector functions. In psoriasis, hallmark features include upregulation of glycolysis, activation of hypoxia-inducible factor-1α (HIF-1α), abnormalities in cholesterol metabolism, and Warburg-like metabolism in keratinocytes. In AD, defects in epidermal ceramide synthesis, impaired essential fatty acid metabolism, disruption of the tryptophan-kynurenine pathway, and abnormal aromatics receptor (AhR) signaling constitute its unique metabolic profile. This article systematically reviews the distinct pathways of metabolic reprogramming in keratinocytes and immune cells in psoriasis and AD, and summarizes the mechanisms of action of key molecules such as mTOR and AMPK. Furthermore, it explores the differential therapeutic potential of metabolism-targeted drugs, including metformin, statins, PPARγ agonists, and AhR modulators. Furthermore, the expression of common regulatory factors such as HIF-1α, PPARγ, and SREBP exhibits opposite trends in the two diseases. Finally, the article discusses the differential therapeutic potential of these metabolite-targeted drugs. This paper compares psoriasis and AD within a unified metabolic immunology framework, aiming to elucidate how these two diseases evolve from similar inflammatory responses into conditions with distinctly different clinical manifestations, and to provide a new theoretical foundation for future metabolism-based personalized therapies.
    Keywords:  AhR; HIF-1α; atopic dermatitis; glycolysis; immunometabolism; lipid metabolism; mTOR; metabolic reprogramming
    DOI:  https://doi.org/10.3389/fimmu.2026.1879634
  31. Microb Pathog. 2026 Jul 31. pii: S0882-4010(26)00467-5. [Epub ahead of print] 108741
      Patients with diabetes mellitus (DM) exhibit increased susceptibility to various infectious diseases, and DM represents a critical underlying risk factor for cryptococcosis. However, how diabetic metabolic dysregulation specifically affects host immune responses against Cryptococcus neoformans remains poorly understood. In this study, we investigated anti-cryptococcal immune responses using a streptozotocin (STZ)-induced DM model established in CnT-II transgenic mice, which harbor abundant Cryptococcus-specific CD4+ T cells. Inducing DM directly in these CnT-II mice enabled direct evaluation of antigen-specific immunity. DM mice, which exhibit decreased systemic reduced glutathione (GSH) under chronic hyperglycemia, showed exacerbated cryptococcal infection, characterized by significantly higher pulmonary fungal burdens, decreased IFN-γ levels, reduced survival rates, and defective granuloma formation. In vitro assays using splenocytes from uninfected DM mice revealed significantly impaired cryptococcal antigen-specific Th1 responses, expanded Treg cells, and increased PD-1 expression on CD4+ T cells compared with controls. Specifically, cross-combination cultures of isolated splenic CD4+ T cells and dendritic cells demonstrated that this Th1 impairment was intrinsic to DM-derived T cells, whereas DM-derived dendritic cells had no effect. Additionally, macrophages cultured under high-glucose conditions showed significantly decreased nitric oxide (NO) production and fungicidal activity. Importantly, exogenous GSH supplementation successfully restored both Th1 differentiation and NO production, whereas Treg cell expansion and defective macrophage fungicidal activity were GSH-independent. Taken together, our findings demonstrate how metabolic redox imbalance compromises coordinated host immunity against C. neoformans, offering potential redox-targeted therapeutic insights for diabetic hosts.
    Keywords:  Cryptococcus neoformans; Th1 immunity; diabetes mellitus; glutathione
    DOI:  https://doi.org/10.1016/j.micpath.2026.108741
  32. Toxics. 2026 Jul 10. pii: 602. [Epub ahead of print]14(7):
      As a major occupational hazard, crystalline silica (SiO2) poses a severe risk of pulmonary toxicity. While the irreversible fibrosis of late-stage silicosis has been extensively studied, the cellular and molecular mechanisms by which SiO2 reprograms macrophage metabolism to drive early pathogenesis remain poorly understood. To elucidate this early immune-inflammatory response, we combined targeted metabolomics, pharmacological treatments, and nutrient deprivation in murine alveolar macrophages. Our results demonstrate that SiO2 exposure severely impairs the master antioxidant regulator, nuclear factor erythroid 2-related factor 2 (Nrf2), triggering excessive reactive oxygen species (ROS) accumulation and upregulated glutamine catabolism to drive pro-inflammatory M1 macrophage polarization. We demonstrated that Nrf2 activation with tert-butylhydroquinone (TBHQ) redirected glutamine metabolic flux from pro-inflammatory catabolism to antioxidant anabolism, significantly attenuating SiO2-induced M1 polarization. Conversely, Nrf2 inhibition via ML385 exacerbated the inflammatory response. Furthermore, introducing a glutamine deprivation (-Gln) model revealed that restricting glutamine availability significantly attenuated the ability of Nrf2 to reverse M1 polarization, suggesting that its immune-protective effects largely depend on an intact glutamine metabolic pathway. Ultimately, our findings underscore the severe risks of silica exposure and identify the Nrf2-glutamine metabolic axis as a promising target, providing novel mechanistic insights and a robust basis for "antioxidant-metabolic" dual-target interventions in early-stage silicosis.
    Keywords:  M1 phenotype; Nrf2; alveolar macrophages; crystalline silica; metabolic reprogramming
    DOI:  https://doi.org/10.3390/toxics14070602
  33. Curr Opin Immunol. 2026 Jul 29. pii: S0952-7915(26)00106-8. [Epub ahead of print]102 102829
      Tumors are spatially heterogeneous ecosystems in which malignant, stromal, vascular, and immune cells interact within metabolically distinct niches. These localized microenvironments are shaped by factors such as nutrient availability, hypoxia, acidosis, and immunomodulatory metabolites, all of which strongly influence CD8⁺ T cell infiltration, migration, persistence, and effector function. Growing evidence indicates that spatial metabolic heterogeneity contributes to immune exclusion, T cell dysfunction, and resistance to immunotherapy. This has been accompanied by major advances in spatial metabolomics, particularly mass spectrometry imaging, which now enable the in situ mapping of metabolites within intact tissues. Combined with transcriptomic, proteomic, and imaging-based approaches, these technologies provide unprecedented insight into how metabolism is organized across tumors and how it shapes tumor-immune interactions. In this review, we discuss how metabolic zonation shapes CD8⁺ T cell function across primary tumors and metastatic lesions. We highlight emerging evidence linking localized metabolic programs to T cell exhaustion, impaired motility, and altered immune composition, and discuss therapeutic strategies aimed at improving T cell metabolic fitness, including metabolic modulation and engineering approaches relevant to immune checkpoint blockade and adoptive cell therapies. Finally, we consider the translational potential of spatial metabolomics for biomarker discovery and the development of precision immunometabolic oncology.
    DOI:  https://doi.org/10.1016/j.coi.2026.102829
  34. J Alzheimers Dis. 2026 Jul 31. 13872877261469862
      Alzheimer's disease (AD) is increasingly recognized as a disorder in which amyloid-β deposition and tau pathology interact with neuroinflammation and metabolic dysregulation. Although mitochondrial dysfunction, redox imbalance, and NLRP3 inflammasome activation have each been implicated in AD pathogenesis, their mechanistic continuity within microglial immunometabolic reprogramming remains insufficiently defined. This narrative review integrates mechanistic, preclinical, and human-relevant evidence to propose a stage-dependent mitochondrial dysfunction-redox imbalance-NLRP3 inflammasome axis. We discuss how AD-related stimuli shift microglia toward a pro-inflammatory metabolic phenotype; how impaired mitochondrial quality control promotes reactive oxygen species generation and oxidized mitochondrial DNA release; and how these signals facilitate NLRP3 inflammasome activation and sustained inflammatory amplification. We further summarize therapeutic strategies targeting upstream mitochondrial homeostasis, intermediate metabolic-redox coupling, and downstream NLRP3 signaling, while emphasizing the translational limitations and biomarker needs. We conclude that this proposed axis provides a testable stage-dependent framework for interpreting chronic, self-amplifying neuroinflammation in AD and may inform biomarker-guided, combinatorial therapeutic strategies.
    Keywords:  Alzheimer's disease; NLRP3 inflammasome; immunometabolic reprogramming; microglia; mitochondrial dysfunction; neuroinflammation; redox imbalance
    DOI:  https://doi.org/10.1177/13872877261469862
  35. Nat Immunol. 2026 Jul 31.
      The mechanisms sustaining chronic inflammation in rheumatoid arthritis (RA) remain incompletely understood. Here we show that branched-chain amino acid (BCAA) catabolism, mediated by the mitochondrial enzyme BCAT2, sustained interferon-driven macrophage activation in autoimmune arthritis. Multi-omics and histological analyses of individuals with active RA or sustained remission revealed that active disease was associated with systemic BCAA depletion, synovial branched-chain ketoacid accumulation and elevated BCAT2 expression in interferon-responsive synovial macrophages. Mechanistically, interferon-γ induced BCAT2 transcription through the transcription factor IRF1 in RA synovial macrophages. In human monocyte-derived macrophages, BCAT2-dependent BCAA catabolism elevated mitochondrial reactive oxygen species, which in turn restrained SHP-1 activity, prolonged STAT1 and STAT2 phosphorylation and drove inflammatory cytokine production. Furthermore, myeloid-specific deletion of Bcat2 ameliorated collagen antibody-induced arthritis in mice. Pharmacological targeting of this pathway with telmisartan suppressed persistent arthritis in methotrexate-treated mice. Together, our findings identified BCAT2-dependent amino acid catabolism as a potentially targetable metabolic pathway in autoimmune arthritis.
    DOI:  https://doi.org/10.1038/s41590-026-02604-5
  36. Transl Oncol. 2026 Jul 27. pii: S1936-5233(26)00289-5. [Epub ahead of print]72 102953
      Ovarian cancer (OC) remains a leading cause of cancer-related mortality among women worldwide, largely due to asymptomatic progression, late-stage diagnosis, therapeutic resistance, and profound immunosuppression within the tumor microenvironment (TME). This is particularly relevant in advanced disease, where metastatic spread to the omentum creates a lipid-rich niche that promotes tumor growth and weakens anti-tumor immunity. This review examines lipid metabolic reprogramming and γδ T-cell function as a targetable immunometabolic axis in OC, with selected discussion of iNKT and CD8+ T-cells as comparative models. Direct evidence from OC patient samples demonstrates that the omental TME drives CD36-mediated lipid uptake and fatty acid (FA) oxidation, while chronic lipid exposure impairs γδ T-cell mitochondrial oxidative phosphorylation and promotes exhaustion, including up-regulation of PD-1 and TIGIT. The major γδ T-cell subsets exhibit distinct metabolic vulnerabilities: Vδ1 T-cells can recognize CD1-presented lipid antigens and rely on FA oxidation, favoring pro-tumoral IL-17 production, whereas Vδ2 T-cells detect phosphoantigens via BTN3A and depend more strongly on glycolysis, rendering them susceptible to glucose deprivation in the OC TME. Concurrent adenosine signaling via A2A receptors, potentially amplified by lipid-induced CD39/CD73 up-regulation, further suppresses γδ T-cell function. We also evaluate nanoparticle-based platforms for co-delivery of metabolic modulators, γδ T-cell agonists, and immune checkpoint blockers, while highlighting key translational barriers, including variable enhanced permeability and retention effects, limited γδ T-cell-specific targeting, and potential systemic toxicity of FASN or CD36 inhibition. Finally, this review proposes future strategies including single-cell metabolomics to map subset-specific vulnerabilities, CRISPR-based validation of exhaustion mechanisms, metabolic engineering of CAR-γδ T-cells through CD36 knockout or CPT1A overexpression, intraperitoneal nanoparticle delivery in patient-derived xenograft models, and TME-restricted delivery systems. Together, these approaches may help overcome lipid-driven immune dysfunction and support the development of next-generation immunotherapies for OC.
    Keywords:  Immunometabolism; Lipid-rich TME; Metabolic exhaustion; Nanoparticles; Ovarian cancer; γδ T-cells
    DOI:  https://doi.org/10.1016/j.tranon.2026.102953
  37. Pathogens. 2026 Jun 26. pii: 680. [Epub ahead of print]15(7):
      Pseudomonas aeruginosa can utilize abundant phosphatidylcholine (PC) and phosphatidylethanolamine (PE) within the host as energy and structural substrates. Fatty acids, choline, and ethanolamine liberated from PC and PE can each serve as the sole carbon source to support bacterial growth in vitro. Our previous work demonstrated that fatty acid metabolism is critical for acute pulmonary infection caused by P. aeruginosa. The pathogen senses host-derived fatty acids via the transcriptional regulator PvrA, which activates fatty acid utilization pathways and drives the production of virulence factors required for acute infection. In this study, we demonstrate that during acute pulmonary infection in mice, P. aeruginosa upregulates fatty acid catabolism while simultaneously repressing choline and ethanolamine uptake and metabolism pathways. Deletion of the transcriptional activators GbdR and EatR (which control choline and ethanolamine utilization respectively) enhances pulmonary bacterial colonization. We further identify fatty acids as environmental signals that trigger repression of choline and ethanolamine utilization programs. PvrA mediates this signaling cascade by directly binding to the promoters of gbdR and eatR and suppressing their transcription upon fatty acid exposure.
    Keywords:  P. aeruginosa; PvrA; fatty acids
    DOI:  https://doi.org/10.3390/pathogens15070680
  38. Cell Rep. 2026 Jul 28. pii: S2211-1247(26)00833-8. [Epub ahead of print]45(8): 117755
      Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection reprograms host metabolism to favor viral replication and immune evasion, yet the contribution of accessory proteins remains poorly defined. Here, we characterize the metabolic effects of the SARS-CoV-2 accessory protein ORF7a. Lentiviral expression of ORF7a in human lung epithelial (A549) and monocytic (THP1) cells, combined with integrated transcriptomic, proteomic, and metabolomic analyses, revealed marked dysregulation of glucose and lipid metabolism. ORF7a impaired mitochondrial oxidative phosphorylation, reducing basal and maximal respiration, inducing mitochondrial depolarization, and increasing reactive oxygen species. Mechanistically, ORF7a upregulated pyruvate dehydrogenase kinase 4 (PDK4), enhancing phosphorylation of the pyruvate dehydrogenase complex and suppressing pyruvate oxidation. However, pharmacological PDK4 inhibition failed to restore respiratory function. High-resolution respirometry identified complex I dysfunction, while Blue Native-PAGE revealed defective assembly of respiratory supercomplexes. Together, these findings demonstrate that ORF7a disrupts mitochondrial metabolism through enzymatic regulation and destabilization of the respiratory chain, highlighting mitochondria as a target of SARS-CoV-2-induced metabolic reprogramming.
    Keywords:  CP: microbiology; ORF7a; SARS-CoV-2; complex I dysfunction; metabolic reprogramming; mitochondrial dysfunction; oxidative phosphorylation; respiratory chain supercomplexes
    DOI:  https://doi.org/10.1016/j.celrep.2026.117755
  39. EBioMedicine. 2026 Jul 31. pii: S2352-3964(26)00286-0. [Epub ahead of print] 106402
       BACKGROUND: d-amino acids (D-AAs), the enantiomers of proteinogenic l-amino acids, are detectable in mammals, yet their biological roles in cancer immunity remain largely unexplored. Whether specific D-AAs modulate tumour progression or influence responsiveness to immunotherapy in gastrointestinal cancer is unknown. We aimed to determine how D-AAs, particularly d-serine (D-ser), shape the tumour immune microenvironment and affect clinical outcomes in gastrointestinal cancers.
    METHODS: Mechanistic studies were conducted using murine MC38 tumours and orthotopic gastric cancer (GC) organoid allografts with or without D-AAs supplementation. Immune landscape alterations were assessed using single-cell RNA sequencing of tumour-infiltrating immune cells, flow cytometry, ex vivo macrophage-T cell co-culture assays, and microbiome manipulation experiments. D-AAs concentrations in plasma, urine, and stool were quantified in healthy controls (HCs; n = 87) and patients with GC across three cohorts (Cohort 1, n = 14; Cohort 2, n = 108; Cohort 3, n = 28). Associations between plasma D-ser levels, disease stage, immune cell infiltration, and clinical outcomes following anti-PD-1 antibody therapy were analysed.
    FINDINGS: D-ser promoted tumour progression by suppressing CD8+ T cell immunity and enhancing SPP1-associated immunosuppressive macrophage signalling in murine model. Across all clinical cohorts, the plasma, urine, and stool levels of several D-AAs, most prominently D-ser, were significantly elevated in patients with GC compared to HCs. Plasma concentration of D-ser strongly correlated with disease stage (I-IV). Elevated plasma D-ser is associated with an immunosuppressive tumour microenvironment and poor response to anti-PD-1 monotherapy in patients with advanced gastric cancer.
    INTERPRETATION: This study identifies D-ser as a previously unrecognised immunosuppressive metabolite that promotes tumour immune evasion by increased macrophages and reduced CD8+ T cell effector function, thereby shifting the tumour microenvironment toward an immunosuppressive phenotype. Clinically, D-ser is a potential metabolite to predict cancer progression and immunotherapy resistance.
    FUNDING: This work was supported by The Japan Science and Technology Agency (JST) Fusion Oriented Research for Disruptive Science and Technology (FOREST)[JPMJFR210P], Grants-in-Aid from the Japanese Society for the Promotion of Science (JSPS) (25K10430, 21K18272, 23H02899, 23K27590, 25K22627), KGRI challenge grant, Sakaguchi Memorial Foundation, Japan Agency for Medical Research and Development (CREST 21gm1510002h0001), and Miyarisan Pharmaceutical Grant.
    Keywords:  CD8(+) T cells; Gastric cancer; Macrophages; Metabolite; d-serine
    DOI:  https://doi.org/10.1016/j.ebiom.2026.106402
  40. Nature. 2026 Jul 29.
      Senescent cells promote tissue dysfunction in part through the senescence-associated secretory phenotype (SASP)1. Cytosolic mitochondrial nucleic acids activate innate immune signalling to initiate this inflammatory programme2,3. Here we show that mitochondrial metabolism provides a second layer of control that enables execution of the inflammatory programme. In senescent cells, the mitochondrial pyruvate-citrate-acetyl-CoA axis is upregulated, increasing the availability of acetyl-CoA to support histone acetylation at SASP genes. Whereas mitochondrial DNA-driven signalling activates inflammatory transcription factors, acetyl-CoA availability is required for robust transcription of SASP genes. Accordingly, enhancing acetyl-CoA levels promotes SASP gene expression, whereas inhibition of SLC25A1, the mitochondrial citrate exporter, reduces histone acetylation at SASP loci, limiting activity of this programme. In vivo, inhibition of SLC25A1 reduces chromatin accessibility at SASP loci, dampens inflammation and improves healthspan in aged mice. Together, these findings identify a mitochondrial metabolic checkpoint that enables the epigenetic execution of innate immune signalling, revealing a mechanism that selectively controls the inflammatory output of senescent cells.
    DOI:  https://doi.org/10.1038/s41586-026-10791-2
  41. Prog Neuropsychopharmacol Biol Psychiatry. 2026 Jul 26. pii: S0278-5846(26)00259-9. [Epub ahead of print] 111861
      Diabetes-associated cognitive impairment (DCI) is an increasingly recognized neurological complication of type 2 diabetes mellitus characterized by chronic neuroinflammation and microglial immunometabolic dysregulation. Vitamin B12 (VB12) deficiency, which is highly prevalent in patients with diabetes, has been strongly associated with cognitive decline, hippocampal atrophy, and white matter injury. Emerging evidence suggests that VB12 plays a critical role in maintaining one‑carbon metabolism, mitochondrial function, and redox homeostasis. Mechanistically, VB12 deficiency promotes homocysteine accumulation, disrupts the S-adenosylmethionine/S-adenosylhomocysteine balance, impairs mitochondrial oxidative phosphorylation, and enhances oxidative stress, thereby driving pro-inflammatory microglial activation and sustained neuroinflammation. In addition, gut microbiota dysbiosis, particularly reduced abundance of Akkermansia muciniphila and other VB12-producing bacteria, may further impair VB12 bioavailability and aggravate neuroinflammation through the gut-brain axis. This review summarizes current evidence linking VB12 deficiency to microglial immunometabolic remodeling in DCI and discusses the therapeutic potential of targeting VB12 metabolism and gut microbial ecology for preventing diabetes-related cognitive decline.
    Keywords:  Akkermansia muciniphila; Diabetes-associated cognitive impairment; Gut–brain axis; Microglial immunometabolic reprogramming; Vitamin B12 deficiency
    DOI:  https://doi.org/10.1016/j.pnpbp.2026.111861
  42. Front Immunol. 2026 ;17 1873690
      Liver transplantation is a life-saving treatment for end-stage liver disease, but long-term outcomes are limited by complications of lifelong immunosuppression. Inducing immune tolerance has become a major research priority. Tryptophan (Trp) metabolism, particularly the kynurenine pathway, is a key endogenous regulator of peripheral tolerance. This review moves beyond a simple description of metabolic routes and provides a critical, integrated analysis. We systematically compare the non-redundant immunosuppressive roles of indoleamine 2,3-dioxygenase (IDO) and tryptophan 2,3-dioxygenase (TDO2) in liver transplant immunity, dissect the Trp/kynurenine/AhR pathways that reprograms immune cell function, and incorporate gut-microbiota-dependent indole metabolism as an upstream gut-liver axis node. Clinical evidence is stratified by level, and major translational barriers, including safety risks, delivery challenges, and lack of validated biomarkers are discussed. Current data suggest that combined metabolite panels may outperform single markers, but therapeutic targeting of Trp metabolism remains a preclinical research direction rather than an established therapy.
    Keywords:  IDO; TDO2; immune tolerance; liver transplantation; tryptophan metabolism
    DOI:  https://doi.org/10.3389/fimmu.2026.1873690
  43. Immunohorizons. 2026 Jul 10. pii: vlag025. [Epub ahead of print]10(7):
      Obesity is increasingly recognized as a state of chronic low-grade inflammation associated with altered immune cell function, yet the mechanisms driving these changes remain incompletely understood. This study investigated myeloid cell subpopulations and neutrophil behavior in adult participants exhibiting preclinical obesity (body mass index [BMI] 32-51 kg/m2, n = 12) compared to normal-weight controls (BMI 21-24 kg/m2, n = 9), correlating findings with metabolic and inflammatory markers. Peripheral blood samples were analyzed by flow cytometry to quantify myeloid cell populations and TLR4/IL-1R surface expression. Neutrophils were cultured under normoxic (18% O2) or hypoxic (1% O2) conditions, with or without glutaminase inhibition, to assess spontaneous neutrophil death. Participants with preclinical obesity exhibited increased monocyte numbers and eosinophils, whereas total neutrophil numbers were not significantly different between groups, together with a higher percentage of HLA-DR-/low monocytes and activated immature (CD16-CD11b+CD10-) neutrophils. In participants under 60 yr of age, IL‑1R expression on monocytes was significantly increased in the obesity group. Significant metabolic differences were also noted, including higher A1c (5.9 ± 0.1% vs 5.3 ± 0.1%), hs-CRP (9.01 ± 3.33 vs 0.69 ± 0.17 mg/L), and alkaline phosphatase (102.33 ± 9.67 vs 65.75 ± 5.54 U/L) in the preclinical obesity cohort, alongside decreased mean cell hemoglobin. Ex vivo neutrophil culture revealed that hypoxia reduced spontaneous neutrophil death in both groups; however, this effect was significantly reduced by glutaminase inhibition specifically in neutrophils from participants with preclinical obesity, suggesting a heightened reliance on glutamine metabolism for survival under hypoxia. These findings demonstrate dysregulated myelopoiesis and altered neutrophil behavior in preclinical obesity, providing mechanistic insight into the early immune consequences of metabolic dysfunction.
    Keywords:  apoptosis; hematopoiesis; human; monocytes/macrophages; neutrophils
    DOI:  https://doi.org/10.1093/immhor/vlag025
  44. Cell Rep. 2026 Jul 30. pii: S2211-1247(26)00779-5. [Epub ahead of print]45(8): 117701
      Heat stroke causes life-threatening systemic inflammation and multiorgan injury, but the intracellular mechanisms that sustain inflammatory amplification after heat exposure remain unclear. Here, using heat stroke mouse models, genetic NLRP3 deletion, pharmacological inhibition, myeloid-specific NLRP3 deficiency, macrophage depletion, and heat-stressed macrophage systems, we show that tissue macrophage NLRP3 inflammasome activation is a central driver of interleukin-1β/interleukin-18 release, organ injury, and mortality. Mechanistically, heat stroke enhances phospholipase C delta 4 signaling, promotes diacylglycerol accumulation at trans-Golgi network/Golgi-associated membranes, recruits protein kinase D1, and increases phosphatidylinositol 4-kinase β-dependent phosphatidylinositol 4-phosphate production. This lipid remodeling supports NLRP3 recruitment, ASC speck formation, caspase-1 activation, and inflammatory cytokine release. Phospholipase C delta 4 knockdown preferentially suppresses NLRP3 activation induced by heat stroke, but not by canonical stimuli. These findings link heat stroke to membrane lipid remodeling and spatial inflammasome assembly, identifying a potential organ-protective pathway in heat stroke.
    Keywords:  CP: immunology; CP: metabolism; NLRP3 inflammasome; PI4KB; PI4P; PLCd4; heat stroke; macrophages; multiorgan injury
    DOI:  https://doi.org/10.1016/j.celrep.2026.117701
  45. Brain Behav Immun Health. 2026 Oct;56 101310
      Vaccination under deliberately varied metabolic conditions provides a framework to identify metabolic determinants of immune response to vaccine and to identify metabolic pathways that may serve as immunomodulators or future adjuvant targets. Suboptimal vaccine immunogenicity and waning antibody durability remain significant public health challenges requiring effective interventions. To examine the association between vaccine immunogenicity and altered metabolic microenvironments, we applied a short-term metabolic intervention coinciding with SARS-CoV-2 immunization. In this randomized trial, half of the participants completed a metabolically targeted 90-min exercise bout immediately post-immunization, a stimulus known to induce sustained shifts in systemic metabolic changes for up to 24 h. Participants in the control group did not exercise after vaccination. Serum anti-RBD IgG antibody and a putative biomarker of germinal center activity (CXCL13) were assessed as measures of immunogenicity in longitudinally collected samples, and metabolic profile was analyzed by Raman spectroscopy. Associations between age, BMI, psychosocial stress and immune response and metabolic profiles were determined. The exercise-metabolic treatment enhanced antibody durability and shifted the kinetics of CXCL13 and serum antibody response in participants without pre-existing immunity. Specific immuno-metabolic signatures distinguished exercise-metabolic treatment from control, identified participants with pre-existing immunity, and revealed effects of age. This study demonstrates the feasibility of a readily accessible short-term metabolic intervention applied at vaccination in shaping in vivo adaptive immunity and provides critical insights into metabolic predictors of immunogenicity. These findings can be used to interrogate further host factor-related metabolic predictors of vaccine response (i.e., age, BMI, stress) and develop innovative vaccine platforms that influence the metabolic microenvironment.
    DOI:  https://doi.org/10.1016/j.bbih.2026.101310
  46. Nat Commun. 2026 07 27. pii: 7404. [Epub ahead of print]17(1):
      Obesity is a major risk factor for colorectal cancer (CRC), yet the mechanisms linking obesity-associated gut dysbiosis to tumor progression remain unclear. Here, we show that a high-fat diet and fecal microbiota from patients with obesity-associated CRC deplete the GABA-producing commensal Bacteroides ovatus, resulting in reduced luminal GABA and accelerated tumorigenesis. Microbial GABA activates epithelial GABAB receptor signaling and induces TPI1 through the PI3K-HIF1α pathway. Increased TPI1-derived glyceraldehyde-3-phosphate inhibits PPP1CA, maintains YAP phosphorylation, restricts nuclear YAP activity, and suppresses pentose phosphate pathway flux, thereby limiting tumor growth. Consistently, obesity-associated CRC exhibits reduced fecal GABA, decreased TPI1 expression, and metabolic rewiring. A GABA-deficient B. ovatus mutant fails to restore GABA or suppress tumors despite normal colonization, whereas oral GABA supplementation or recolonization with wild-type B. ovatus markedly reduces tumor burden. These findings identify a microbiota-neurotransmitter-metabolism axis linking obesity to CRC and suggest microbiota-based GABA restoration as a potential preventive strategy.
    DOI:  https://doi.org/10.1038/s41467-026-76079-1
  47. Cell Death Differ. 2026 Jul 31.
      The development and functional maintenance of CD8+ T cells are metabolically regulated processes in which mitochondria serve as the central hub. Here, we identify glucose-regulated protein 75 (GRP75) as a critical mitochondrial regulator controlling these processes. Using T cell-specific Hspa9 (encodes GRP75) knockout mice, we demonstrate that GRP75 deficiency disrupts CD8+ T cell fate, leading to defective T cell homeostasis and impaired memory differentiation. Mechanistically, impaired mitochondrial function in GRP75-deficient CD8+ T cells leads to perturbation of IL-7R signaling and aberrant expression of effector-associated molecules. Further studies reveal that GRP75 deficiency leads to upregulation of interferon regulatory factor 4 (IRF4), a critical transcription factor for effector versus memory fate, which in turn suppresses memory CD8+ T cell differentiation. Our findings establish GRP75 as a pivotal mitochondrial checkpoint that coordinates metabolic state and functional fate in CD8+ T cells.
    DOI:  https://doi.org/10.1038/s41418-026-01830-6
  48. Cell Rep. 2026 Jul 27. pii: S2211-1247(26)00831-4. [Epub ahead of print]45(8): 117753
      Fungal spores maintain viability and then germinate to infect host plants, but how these biological processes are integrated remains elusive. Here, we show that γ-carboxymuconolactone decarboxylase 1 (FolCmd1) is an acetylated protein reversibly regulated by the controlling enzymes in the devastating soil-borne pathogen Fusarium oxysporum. FolCmd1 is largely acetylated and imported into the nucleus by FolFkbp4, thereby avoiding excessive metabolism of aromatic amino acids that are critical for long-term survival of spores. During invasion, FolCmd1 is deacetylated and translocated into the cytoplasm to remove host-derived ferulic acid, thus enabling spore germination. Consequently, dysacetylation of FolCmd1 leads to impaired virulence. These findings reveal a sophisticated pathogenic mechanism by coordinating two developmental stages through dynamic modification of a metabolic enzyme.
    Keywords:  CP: microbiology; FA detoxification; plant-microbe interactions; post-translational modification; spore stability; virulence; wilt disease
    DOI:  https://doi.org/10.1016/j.celrep.2026.117753
  49. Autoimmun Rev. 2026 Jul 29. pii: S1568-9972(26)00164-3. [Epub ahead of print] 104150
      Hepato-biliary-pancreatic cancers, notorious for their pronounced heterogeneity and poor prognosis, continue to be a dominant factor in cancer-related deaths globally. Although immunotherapy has dramatically reshaped the cancer treatment landscape, its efficacy in these malignancies remains suboptimal due to the intense immunosuppression in the tumor microenvironment (TME) stemming from metabolic dysregulation. This review provides an in-depth analysis of the fundamental mechanisms of immunometabolic suppression. It highlights the strategies employed by tumor cells to compete with immune cells for nutrients, the accumulation of inhibitory metabolitessuch as lactate and adenosine, and disrupt pivotal metabolic pathways in CD8+ T, NK, and myeloid cells, ultimately leading to functional depletion. The novelty of this work lies in its systematic classification of these metabolic vulnerabilities and the introduction of a tripartite approach to address them: nutrient redistribution, metabolite scavenging, and enhancement of immune cell intrinsic metabolism. This approach aims to complement the next generation of immunotherapies, converting immunologically "cold" tumors into "hot" ones. Additionally, the review emphasizes the potential of integrating multi-omics profiling, artificial intelligence, and biomarker-guided personalized therapy as avenues to overcome resistance and enhance clinical efficacy. By viewing the challenge of therapy resistance through a metabolic perspective, this study not only enriches our foundational understanding of tumor-immune interactions but also presents a practical framework for designing highly efficacious combination therapies, representing a crucial advancement in the management of these formidable cancers.
    Keywords:  CAR-T; Hepato biliary pancreatic tumors; Immune checkpoint inhibitors; Immune metabolism; Metabolic vulnerability; Tumor microenvironment
    DOI:  https://doi.org/10.1016/j.autrev.2026.104150
  50. Infect Dis Immun. 2026 Apr;6(2): 122-137
       Background: Immunometabolism plays a vital role in the immunopathogenesis of people living with human immunodeficiency virus type 1 (HIV-1) (PLWH). However, the precise relationship between metabolic profiles and T-cell dysfunction in this population remains unclear. This study aimed to investigate the metabolic reprogramming and underlying mechanisms contributing to T-cell dysfunction in PLWH, highlighting potential pathogenic mechanisms during chronic HIV-1 infection.
    Methods: This study re-analyzed single-cell RNA sequencing data from the Genome Sequence Archive of the Beijing Institute of Genomics Data Center, Chinese Academy of Sciences. The dataset comprised samples from healthy donors (HD), HIV-1-infected treatment-naive patients (TN), and patients undergoing antiviral therapy. Various analytical approaches-including functional analysis, transcription factor analysis, network analysis, and enrichment analysis-were performed to assess T-cell functional and metabolic characteristics, as well as to identify potential targets within metabolic-epigenetic or non-epigenetic regulatory axes involved in T-cell dysfunction.
    Results: By analyzing the transcriptional profiles, a total of 58,752 CD4+ T cells and 68,907 CD8+ T cells were identified and annotated. Among these, the naive subset CD8-CCR7 was significantly reduced in TN patients compared to HD (P < 0.05), whereas CD4-CCR7 showed a decreasing trend. Conversely, the effector subset CD8+ activated effector/memory T cells (CD8-EMRA) were significantly increased in TN patients (P < 0.05), while cytolytic CD4+ T cells (CD4-CTL) displayed an increasing trend. ART did not effectively reverse these alterations. Additionally, naive subsets and CD8-EMRA cells were associated with disease progression. Further analysis revealed that naive subsets exhibited hyper-activation and increased differentiation, whereas effector subsets showed excessive activation and a strong interferon (IFN) response in PLWH compared to HD (P < 0.05). Intriguingly, we observed substantial metabolic alterations linked to immune dysfunction within the four T-cell subsets. Specifically, elevated levels of the methyltransferases absent, small, or homeotic-like 1 (ASH1L) and SET domain containing 1B (SETD1B) may have promoted the differentiation and exhaustion of the CD4-CCR7 subset via the ASH1L/SETD1B-H3K4me3-FOXP1 axis. These enzymes were also associated with the exhaustion of CD8-CCR7 cells in TN patients through ASH1L/SETD1B-H3K4me3 axis. Additionally, isocitrate dehydrogenase 2 (IDH2)-mediated production of α-ketoglutarate (α-KG) may have contributed to the dysfunction of CD8-CCR7 cells by activating Janus kinase (JAK)-signal transducer and activator of transcription (STAT)3-dependent interferon signaling during HIV-1 infection. Conversely, increased activity of SET domain containing 2 methyltransferase was closely linked to hyperactivation, a strong type I interferon response, and cellular senescence in CD4-CTL cells from TN patients. Furthermore, heightened expression of solute carrier family 7 member 5 correlated with exhaustion of effector subsets in TN individuals. The IDH2-STAT1 axis may have also played a crucial role in driving the over-activation and exhaustion of CD8-EMRA cells through interferon signaling pathways.
    Conclusion: These findings indicate that amino acid- and IDH2-related metabolism may contribute to the dysfunction of both naive and effector subsets by metabolic-epigenetic or non-epigenetic regulatory axes in PLWH.
    Keywords:  HIV; Human metabolism; Immunology; Virology
    DOI:  https://doi.org/10.1097/ID9.0000000000000189