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Programmed death 1 protects from fatal circulatory failure during systemic virus infection of mice

https://doi.org/10.1084/jem.20121015

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Control of Toxoplasma reactivation by rescue of dysfunctional CD8 + T-cell response via PD-1–PDL-1 blockade

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Nitric Oxide Inhibits Hepatitis B Virus Replication in the Livers of Transgenic Mice

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Physiological and Immunologic Disturbances Associated with Shock in a Primate Model of Lassa Fever

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inferredcites →https://doi.org/10.1093/intimm/10.10.1563openalex-snapshot

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inferredcites →https://doi.org/10.1128/jvi.79.10.5979-5987.2005openalex-snapshot

Characterization of the Interaction of Lassa Fever Virus with Its Cellular Receptor α-Dystroglycan

inferredcites →https://doi.org/10.1146/annurev-pathol-011110-130158openalex-snapshot

The Acute Respiratory Distress Syndrome: Pathogenesis and Treatment

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Plasma leakage in dengue haemorrhagic fever

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inferredcites →https://doi.org/10.1172/jci40040openalex-snapshot

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inferredcites →https://doi.org/10.1172/jci44872openalex-snapshot

New therapy to revert dysfunctional antibody responses during HIV-1 infection

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Endothelial cells in physiology and in the pathophysiology of vascular disorders.

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Pathogenesis of lassa fever in cynomolgus macaques

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T Cell-Dependence of Lassa Fever Pathogenesis

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Programmed Death (PD)-1-Deficient Mice Are Extremely Sensitive to Murine Hepatitis Virus Strain-3 (MHV-3) Infection

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Chronic Antigen Stimulation Alone Is Sufficient to Drive CD8+ T Cell Exhaustion

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Expression of the inducible nitric oxide synthase. Correlation with neuropathology and clinical features in mice with lymphocytic choriomeningitis.

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Detrimental Contribution of the Immuno-Inhibitor B7-H1 to Rabies Virus Encephalitis

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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TOX transcriptionally and epigenetically programs CD8+ T cell exhaustion

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TOX reinforces the phenotype and longevity of exhausted T cells in chronic viral infection

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MYB orchestrates T cell exhaustion and response to checkpoint inhibition

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Endogenous glucocorticoids control host resistance to viral infection through the tissue-specific regulation of PD-1 expression on NK cells

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Not-so-opposite ends of the spectrum: CD8+ T cell dysfunction across chronic infection, cancer and autoimmunity

inferred← citeshttps://doi.org/10.1038/s41590-022-01219-wopenalex-snapshot

‘Stem-like’ precursors are the fount to sustain persistent CD8+ T cell responses

inferred← citeshttps://doi.org/10.1038/s41590-024-01961-3openalex-snapshot

Epigenetic tuning of PD-1 expression improves exhausted T cell function and viral control

inferred← citeshttps://doi.org/10.1038/s41590-025-02276-7openalex-snapshot

Lymph nodes fuel KLF2-dependent effector CD8+ T cell differentiation during chronic infection and checkpoint blockade

inferred← citeshttps://doi.org/10.1038/s42255-020-00280-9openalex-snapshot

Metabolic and epigenetic regulation of T-cell exhaustion

inferred← citeshttps://doi.org/10.1073/pnas.1408148111openalex-snapshot

Type I interferon is a therapeutic target for virus-induced lethal vascular damage

inferred← citeshttps://doi.org/10.1073/pnas.1718217115openalex-snapshot

Role of PD-1 during effector CD8 T cell differentiation

inferred← citeshttps://doi.org/10.1080/20013078.2020.1792683openalex-snapshot

In vivo identification of apoptotic and extracellular vesicle‐bound live cells using image‐based deep learning

inferred← citeshttps://doi.org/10.1080/2162402x.2017.1371399openalex-snapshot

TIGIT expressing CD4+T cells represent a tumor-supportive T cell subset in chronic lymphocytic leukemia

inferred← citeshttps://doi.org/10.1080/2162402x.2024.2344905openalex-snapshot

The potential role of CMC1 as an immunometabolic checkpoint in T cell immunity

inferred← citeshttps://doi.org/10.1084/jem.20121416openalex-snapshot

PD-1 promotes immune exhaustion by inducing antiviral T cell motility paralysis

inferred← citeshttps://doi.org/10.1084/jem.20132577openalex-snapshot

Interplay between regulatory T cells and PD-1 in modulating T cell exhaustion and viral control during chronic LCMV infection

inferred← citeshttps://doi.org/10.1084/jem.20142237openalex-snapshot

Genetic absence of PD-1 promotes accumulation of terminally differentiated exhausted CD8+ T cells

inferred← citeshttps://doi.org/10.1084/jem.20150598openalex-snapshot

High antigen levels induce an exhausted phenotype in a chronic infection without impairing T cell expansion and survival

inferred← citeshttps://doi.org/10.1084/jem.20180654openalex-snapshot

IFNγ-activated dermal lymphatic vessels inhibit cytotoxic T cells in melanoma and inflamed skin

inferred← citeshttps://doi.org/10.1084/jem.20241133openalex-snapshot

BCOR and ZC3H12A suppress a core stemness program in exhausted CD8+ T cells

inferred← citeshttps://doi.org/10.1093/eurheartj/ehaf1080openalex-snapshot

T cells in acute and chronic myocarditis: from diagnosis to treatment

inferred← citeshttps://doi.org/10.1093/infdis/jiab274openalex-snapshot

Anti–PD-L1 Therapy Does Not Improve Survival in a Murine Model of Lethal Staphylococcus aureus Pneumonia

inferred← citeshttps://doi.org/10.1093/infdis/jiu215openalex-snapshot

Postnatal Acquisition of Primary Rhesus Cytomegalovirus Infection is Associated With Prolonged Virus Shedding and Impaired CD4+ T Lymphocyte Function

inferred← citeshttps://doi.org/10.1093/intimm/dxaa039openalex-snapshot

Impact of multiple hits with cognate antigen on memory CD8+ T-cell fate

inferred← citeshttps://doi.org/10.1093/intimm/dxac050openalex-snapshot

Population dynamics and gene regulation of T cells in response to chronic antigen stimulation

inferred← citeshttps://doi.org/10.1093/jimmun/vkaf210openalex-snapshot

Lpar5 regulates the CD8 T-cell response to persistent virus infection by altering exhaustion programming, survival, and NK receptor expression

inferred← citeshttps://doi.org/10.1093/jleuko/qiae256openalex-snapshot

Protective function of ex vivo-expanded CD8 T cells in a mouse model of adoptive therapy for cytomegalovirus infection depends on integrin beta 1 but not CXCR3, CTLA4, or PD-1 expression

inferred← citeshttps://doi.org/10.1093/ofid/ofae183openalex-snapshot

Exacerbation of CMV and Nontuberculous Mycobacterial Infections Following PD-1 Blockade for HIV-Associated Kaposi Sarcoma

inferred← citeshttps://doi.org/10.1093/oncolo/oyab083openalex-snapshot

Impact of Immune Checkpoint Inhibitors on COVID-19 Severity in Patients with Cancer

inferred← citeshttps://doi.org/10.1101/2020.02.22.960278openalex-snapshot

Latent Plasticity of Effector-like Exhausted CD8 T cells contributes to memory responses

inferred← citeshttps://doi.org/10.1101/2024.03.16.585350openalex-snapshot

Protective function of ex vivo expanded CD8 T cells in a mouse model of adoptive therapy for cytomegalovirus infection depends on integrin beta 1 but not CXCR3, CTLA4, or PD-1 expression

inferred← citeshttps://doi.org/10.1101/2025.02.17.634430openalex-snapshot

Themis dominates T cell exhaustion by regulation of TCR and PD-1 signaling

inferred← citeshttps://doi.org/10.1101/2025.03.10.642460openalex-snapshot

Humanizing a CD28 signaling domain affects CD8 activation, exhaustion and stem-like precursors

inferred← citeshttps://doi.org/10.1101/2025.08.06.668764openalex-snapshot

Angiogenic CD8 T cells from PWH induce Granzymes-dependent PAR1 activation promoting endothelial inflammation

inferred← citeshttps://doi.org/10.1101/2025.10.19.683142openalex-snapshot

CD8 T cells mediate immunosurveillance for neoantigen+ epithelial stem cells in the colon

inferred← citeshttps://doi.org/10.1111/1759-7714.12494openalex-snapshot

Nivolumab infusion reaction manifesting as plantar erythema and pulmonary infiltrate in a lung cancer patient

inferred← citeshttps://doi.org/10.1111/bjh.18095openalex-snapshot

Resolving sticky relationships between platelets and lymphocytes in COVID‐19 : A role for checkpoint inhibitors?

inferred← citeshttps://doi.org/10.1111/febs.15756openalex-snapshot

Dampening antiviral immunity can protect the host

inferred← citeshttps://doi.org/10.1111/imm.12739openalex-snapshot

CD8 T‐cell regulation by T regulatory cells and the programmed cell death protein 1 pathway

inferred← citeshttps://doi.org/10.1111/imr.13203openalex-snapshot

T‐cell heterogeneity, progenitor–progeny relationships, and function during latent and chronic viral infections

inferred← citeshttps://doi.org/10.1111/imr.13388openalex-snapshot

Immune checkpoint inhibitors in infectious disease

inferred← citeshttps://doi.org/10.1111/joim.13006openalex-snapshot

Beyond neurotransmission: acetylcholine in immunity and inflammation

inferred← citeshttps://doi.org/10.1111/sji.12036openalex-snapshot

Identification of new internalizing surface receptors on human dendritic cells by phage display antibodies

inferred← citeshttps://doi.org/10.1126/science.aaa7516openalex-snapshot

RETRACTED: The protein LEM promotes CD8 + T cell immunity through effects on mitochondrial respiration

inferred← citeshttps://doi.org/10.1126/science.aac4997openalex-snapshot

Expanding the role of metabolism in T cells

inferred← citeshttps://doi.org/10.1126/sciimmunol.abf3861openalex-snapshot

PD-1 blockade exacerbates Mycobacterium tuberculosis infection in rhesus macaques

inferred← citeshttps://doi.org/10.1126/sciimmunol.adg3868openalex-snapshot

Cellular and molecular waypoints along the path of T cell exhaustion

inferred← citeshttps://doi.org/10.1126/scitranslmed.aba6006openalex-snapshot

Metabolic regulation by PD-1 signaling promotes long-lived quiescent CD8 T cell memory in mice

inferred← citeshttps://doi.org/10.1128/jvi.01263-17openalex-snapshot

Differential Inhibitory Receptor Expression on T Cells Delineates Functional Capacities in Chronic Viral Infection

inferred← citeshttps://doi.org/10.1128/jvi.02103-17openalex-snapshot

Adenovirus Vector Vaccination Impacts NK Cell Rheostat Function following Lymphocytic Choriomeningitis Virus Infection

inferred← citeshttps://doi.org/10.1128/jvi.03002-13openalex-snapshot

Therapeutic Depletion of Natural Killer Cells Controls Persistent Infection

inferred← citeshttps://doi.org/10.1146/annurev-immunol-041015-055318openalex-snapshot

CD8 T Cell Exhaustion During Chronic Viral Infection and Cancer

inferred← citeshttps://doi.org/10.1146/annurev-immunol-082223-044122openalex-snapshot

Molecular Mechanisms Governing CD8 T Cell Differentiation and Checkpoint Inhibitor Response in Cancer

inferred← citeshttps://doi.org/10.1146/annurev-immunol-090222-110914openalex-snapshot

T Cell Exhaustion

inferred← citeshttps://doi.org/10.1146/annurev-immunol-101721-064501openalex-snapshot

Extremely Differentiated T Cell Subsets Contribute to Tissue Deterioration During Aging

inferred← citeshttps://doi.org/10.1172/jci.insight.181063openalex-snapshot

Prothrombin prevents fatal T cell–dependent anemia during chronic virus infection of mice

inferred← citeshttps://doi.org/10.1172/jci125297openalex-snapshot

Sphingosine kinase 2 restricts T cell immunopathology but permits viral persistence

inferred← citeshttps://doi.org/10.1186/1742-4690-10-31openalex-snapshot

Molecular signatures of T-cell inhibition in HIV-1 infection

inferred← citeshttps://doi.org/10.1186/s12951-025-03766-4openalex-snapshot

Nanomedicine targeting the PD-1/PD-L1 axis in autoimmune diseases: breaking conventional barriers to restore immune tolerance

inferred← citeshttps://doi.org/10.1186/s12964-016-0160-zopenalex-snapshot

T cell exhaustion: from pathophysiological basics to tumor immunotherapy

inferred← citeshttps://doi.org/10.1186/s40001-025-02694-1openalex-snapshot

The PD-1/PD-L1 pathway and Epstein–Barr virus

inferred← citeshttps://doi.org/10.1189/jlb.4ri0214-126ropenalex-snapshot

Immune control and failure in HCV infection—tipping the balance

inferred← citeshttps://doi.org/10.1200/edbk-25-481556openalex-snapshot

One Step Ahead: Preventing Tumor Adaptation to Immune Therapy

inferred← citeshttps://doi.org/10.12659/msm.910388openalex-snapshot

Correlation of T Cell Immunoglobulin and ITIM Domain (TIGIT) and Programmed Death 1 (PD-1) with Clinicopathological Characteristics of Renal Cell Carcinoma May Indicate Potential Targets for Treatment

inferred← citeshttps://doi.org/10.1371/journal.ppat.1005224openalex-snapshot

PD-L1 Expression on Retrovirus-Infected Cells Mediates Immune Escape from CD8+ T Cell Killing

inferred← citeshttps://doi.org/10.1371/journal.ppat.1005656openalex-snapshot

Chimeric Mice with Competent Hematopoietic Immunity Reproduce Key Features of Severe Lassa Fever

inferred← citeshttps://doi.org/10.1371/journal.ppat.1005667openalex-snapshot

CD4 T Cell-Derived IFN-γ Plays a Minimal Role in Control of Pulmonary Mycobacterium tuberculosis Infection and Must Be Actively Repressed by PD-1 to Prevent Lethal Disease

inferred← citeshttps://doi.org/10.1371/journal.ppat.1006498openalex-snapshot

Host genetics play a critical role in controlling CD8 T cell function and lethal immunopathology during chronic viral infection

inferred← citeshttps://doi.org/10.1371/journal.ppat.1008525openalex-snapshot

Contribution of STAT1 to innate and adaptive immunity during type I interferon-mediated lethal virus infection

inferred← citeshttps://doi.org/10.1371/journal.ppat.1009349openalex-snapshot

PD-1 is imprinted on cytomegalovirus-specific CD4+ T cells and attenuates Th1 cytokine production whilst maintaining cytotoxicity

inferred← citeshttps://doi.org/10.1371/journal.ppat.1009892openalex-snapshot

Immunological exhaustion: How to make a disparate concept operational?

inferred← citeshttps://doi.org/10.17537/icmbb24.27openalex-snapshot

Investigation of immune response on LCMV infection using mathematical modelling

inferred← citeshttps://doi.org/10.18632/oncotarget.15489openalex-snapshot

Vitamin D increases programmed death receptor-1 expression in Crohn’s disease

inferred← citeshttps://doi.org/10.20892/j.issn.2095-3941.2020.0338openalex-snapshot

Exhausted T cells and epigenetic status

inferred← citeshttps://doi.org/10.21037/aob-21-2openalex-snapshot

Destiny of CD8+ T cells exhaustion in cancer, and rescue of it: a narrative review

inferred← citeshttps://doi.org/10.2174/1389450116666150825110532openalex-snapshot

Innate and Adaptive Immune Responses in Chronic HCV Infection

inferred← citeshttps://doi.org/10.21873/invivo.13055openalex-snapshot

Age-related Differences in Immune Reactions to SARS-CoV-2 Spike and Nucleocapsid Antigens

inferred← citeshttps://doi.org/10.2310/jim.0000000000000059openalex-snapshot

Ninety-Day Survival Rate of Patients with Sepsis Relates to Programmed Cell Death 1 Genetic Polymorphism rs11568821

inferred← citeshttps://doi.org/10.24884/1682-6655-2025-24-3-13-25openalex-snapshot

Effect of Tumor Necrosis Factor Alpha Inhibitor and Interleukin-6 Inhibitor Therapy on Endothelial Dysfunction in Patients with Rheumatoid Arthritis

inferred← citeshttps://doi.org/10.32469/10355/88918openalex-snapshot

Virus interactions with the sphingolipid network : sphingosine kinase 2 in immunosuppression, immunopathology, and viral propagation

inferred← citeshttps://doi.org/10.33594/000000554openalex-snapshot

Insights into Virus-Induced Immune Mediated Liver Pathology

inferred← citeshttps://doi.org/10.33696/immunology.6.194openalex-snapshot

T cell-Intrinsic Peripheral Tolerance: A Checkpoint Target to Treat Autoimmunity

inferred← citeshttps://doi.org/10.3389/fcimb.2019.00207openalex-snapshot

The PD-1/PD-L1 Axis and Virus Infections: A Delicate Balance

inferred← citeshttps://doi.org/10.3389/fcvm.2025.1646968openalex-snapshot

Myocardial infarction with nonobstructive coronary arteries due to acute coronary vasospasm induced by toripalimab: a case report and review of literature

inferred← citeshttps://doi.org/10.3389/fendo.2026.1861245openalex-snapshot

Ocular manifestations and immunological profiles of thyroid eye disease with lacrimal gland enlargement

inferred← citeshttps://doi.org/10.3389/fimmu.2013.00455openalex-snapshot

Inhibitory Receptor Expression Depends More Dominantly on Differentiation and Activation than “Exhaustion” of Human CD8 T Cells

inferred← citeshttps://doi.org/10.3389/fimmu.2015.00310openalex-snapshot

Inhibitory Receptors Beyond T Cell Exhaustion

inferred← citeshttps://doi.org/10.3389/fimmu.2015.00603openalex-snapshot

T Lymphocyte–Endothelial Interactions: Emerging Understanding of Trafficking and Antigen-Specific Immunity

inferred← citeshttps://doi.org/10.3389/fimmu.2016.00564openalex-snapshot

Type I Interferon Impairs Specific Antibody Responses Early during Establishment of LCMV Infection

inferred← citeshttps://doi.org/10.3389/fimmu.2017.01597openalex-snapshot

PD-1/PD-L1 Blockade: Have We Found the Key to Unleash the Antitumor Immune Response?

inferred← citeshttps://doi.org/10.3389/fimmu.2018.02560openalex-snapshot

Hantavirus-Driven PD-L1/PD-L2 Upregulation: An Imperfect Viral Immune Evasion Mechanism

inferred← citeshttps://doi.org/10.3389/fimmu.2018.02642openalex-snapshot

Disruption of IL-33 Signaling Limits Early CD8+ T Cell Effector Function Leading to Exhaustion in Murine Hemophagocytic Lymphohistiocytosis

inferred← citeshttps://doi.org/10.3389/fimmu.2018.02662openalex-snapshot

Non-hematopoietic Control of Peripheral Tissue T Cell Responses: Implications for Solid Tumors

inferred← citeshttps://doi.org/10.3389/fimmu.2019.00054openalex-snapshot

The PD-1/PD-L1 Pathway Affects the Expansion and Function of Cytotoxic CD8+ T Cells During an Acute Retroviral Infection

inferred← citeshttps://doi.org/10.3389/fimmu.2019.00491openalex-snapshot

A Threshold Model for T-Cell Activation in the Era of Checkpoint Blockade Immunotherapy

inferred← citeshttps://doi.org/10.3389/fimmu.2019.01181openalex-snapshot

Can Immunogenic Chemotherapies Relieve Cancer Cell Resistance to Immune Checkpoint Inhibitors?

inferred← citeshttps://doi.org/10.3389/fimmu.2019.02298openalex-snapshot

The Diverse Function of PD-1/PD-L Pathway Beyond Cancer

inferred← citeshttps://doi.org/10.3389/fimmu.2019.02468openalex-snapshot

SHP-2 in Lymphocytes' Cytokine and Inhibitory Receptor Signaling

inferred← citeshttps://doi.org/10.3389/fimmu.2020.00487openalex-snapshot

The Role of PD-1 in Acute and Chronic Infection

inferred← citeshttps://doi.org/10.3389/fimmu.2020.00986openalex-snapshot

Profiling Virus-Specific Tcf1+ T Cell Repertoires During Acute and Chronic Viral Infection

inferred← citeshttps://doi.org/10.3389/fimmu.2021.765730openalex-snapshot

The New Old CD8+ T Cells in the Immune Paradox of Pregnancy

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1029438openalex-snapshot

Role of regulation of PD-1 and PD-L1 expression in sepsis

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1198551openalex-snapshot

Hierarchical transcriptional network governing heterogeneous T cell exhaustion and its implications for immune checkpoint blockade

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1285554openalex-snapshot

Immune checkpoints in rheumatoid arthritis: progress and promise

inferred← citeshttps://doi.org/10.3389/fimmu.2026.1743170openalex-snapshot

Memory-like CD8+ T cells lacking PD-1 adapt to persistent stimulation by reducing TCR signal transduction rather than increasing exhaustion

inferred← citeshttps://doi.org/10.3389/fmicb.2014.00733openalex-snapshot

Endothelial cell dysfunction in viral hemorrhage and edema

inferred← citeshttps://doi.org/10.3390/biomedicines9030260openalex-snapshot

Hypoxia/HIF Modulates Immune Responses

inferred← citeshttps://doi.org/10.3390/cancers11010055openalex-snapshot

Exploiting NK Cell Surveillance Pathways for Cancer Therapy

inferred← citeshttps://doi.org/10.3390/ijms21144918openalex-snapshot

Allosterism of Nicotinic Acetylcholine Receptors: Therapeutic Potential for Neuroinflammation Underlying Brain Trauma and Degenerative Disorders

inferred← citeshttps://doi.org/10.3390/ijms21218159openalex-snapshot

Delicate Role of PD-L1/PD-1 Axis in Blood Vessel Inflammatory Diseases: Current Insight and Future Significance

inferred← citeshttps://doi.org/10.3390/molecules25204831openalex-snapshot

Targeting Metabolism in Cancer Cells and the Tumour Microenvironment for Cancer Therapy

inferred← citeshttps://doi.org/10.3390/nu16234143openalex-snapshot

Polyphenols as Immunomodulators and Epigenetic Modulators: An Analysis of Their Role in the Treatment and Prevention of Breast Cancer

inferred← citeshttps://doi.org/10.3390/v11100885openalex-snapshot

Viral Infections and Autoimmune Disease: Roles of LCMV in Delineating Mechanisms of Immune Tolerance

inferred← citeshttps://doi.org/10.3390/v16030390openalex-snapshot

CD8+ T Cells Mediate Lethal Lung Pathology in the Absence of PD-L1 and Type I Interferon Signalling following LCMV Infection

inferred← citeshttps://doi.org/10.3390/vaccines11101563openalex-snapshot

Usp22 Deficiency Leads to Downregulation of PD-L1 and Pathological Activation of CD8+ T Cells and Causes Immunopathology in Response to Acute LCMV Infection

inferred← citeshttps://doi.org/10.3410/f.726579120.793545055openalex-snapshot

Faculty Opinions recommendation of High antigen levels induce an exhausted phenotype in a chronic infection without impairing T cell expansion and survival.

inferred← citeshttps://doi.org/10.4049/jimmunol.1402180openalex-snapshot

Programmed Death-1 Controls T Cell Survival by Regulating Oxidative Metabolism

inferred← citeshttps://doi.org/10.4049/jimmunol.1403237openalex-snapshot

CD4 T Cell Depletion Substantially Augments the Rescue Potential of PD-L1 Blockade for Deeply Exhausted CD8 T Cells

inferred← citeshttps://doi.org/10.4049/jimmunol.1502018openalex-snapshot

Vaccine Targeting of Subdominant CD8+ T Cell Epitopes Increases the Breadth of the T Cell Response upon Viral Challenge, but May Impair Immediate Virus Control

inferred← citeshttps://doi.org/10.4049/jimmunol.1601464openalex-snapshot

Conserved Region C Functions To Regulate PD-1 Expression and Subsequent CD8 T Cell Memory

inferred← citeshttps://doi.org/10.4049/jimmunol.2300396openalex-snapshot

Neonatal CD8+ T Cells Resist Exhaustion during Chronic Infection

inferred← citeshttps://doi.org/10.4049/jimmunol.2300462openalex-snapshot

SHP-1 Regulates CD8+ T Cell Effector Function but Plays a Subtle Role with SHP-2 in T Cell Exhaustion Due to a Stage-Specific Nonredundant Functional Relay

inferred← citeshttps://doi.org/10.4049/jimmunol.2300785openalex-snapshot

Altering β Cell Antigen Exposure to Exhausted CD8+ T Cells Prevents Autoimmune Diabetes in Mice

inferred← citeshttps://doi.org/10.53846/goediss-7670openalex-snapshot

The Role of Glycolysis in shaping the Autoimmune Potential of Myelin-Reactive T Cells in the Course of Experimental Autoimmune Encephalomyelitis

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