Precursors of exhausted T cells are pre-emptively formed in acute infection
10.1038/s41586-024-08451-4 · doi-reference
Target-dependent B7-H1 regulation contributes to clearance of central nervous system infection and dampens morbidity
10.4049/jimmunol.0803557 · doi-reference
Detrimental contribution of the immuno-inhibitor B7-H1 to rabies virus encephalitis
10.4049/jimmunol.180.11.7506 · doi-reference
Acute viral respiratory infection rapidly induces a CD8+ T cell exhaustion-like phenotype
10.4049/jimmunol.1403004 · doi-reference
Targeting the host response in sepsis: current approaches and future evidence
10.1186/s13054-023-04762-6 · doi-reference
Restoration of T cell function in multi-drug resistant bacterial sepsis after interleukin-7, anti-PD-L1, and OX-40 administration
10.1371/journal.pone.0199497 · doi-reference
TIM3 mediates T cell exhaustion during Mycobacterium tuberculosis infection
10.1371/journal.ppat.1005490 · doi-reference
Phenotypic T cell exhaustion in a murine model of bacterial infection in the setting of pre-existing Malignancy
10.1371/journal.pone.0093523 · doi-reference
CD8+ T cell exhaustion, suppressed gamma interferon production, and delayed memory response induced by chronic Brucella melitensis infection
10.1128/iai.01184-15 · doi-reference
Cytokine storm promoting T cell exhaustion in severe COVID-19 revealed by single cell sequencing data analysis
10.1093/pcmedi/pbac014 · doi-reference
Early effects of HTLV-1 infection on the activation, exhaustion, and differentiation of T-cells in humanized NSG mice
10.3390/cells10102514 · doi-reference
Human T-cell lymphotropic/leukemia virus type 1 (HTLV-1) Tax-specific T-cell exhaustion in HTLV-1-infected individuals
10.1111/cas.13654 · doi-reference
CD8+ T-cell exhaustion phenotype in chronic hepatitis C virus infection is associated with epitope sequence variation
10.3389/fimmu.2022.832206 · doi-reference
mRNA vaccination overcomes hemozoin-mediated impairment of whole parasite vaccine efficacy for malaria
10.1101/2025.10.29.685344 · doi-reference
PARP1-NFATc1-PD1 pathway of maturation and stability of CD8+T cells is beneficial against chronic Trypanosoma cruzi infection
10.1016/j.isci.2025.112926 · doi-reference
Blockade of LAG-3 in PD-L1-deficient mice enhances clearance of blood stage malaria independent of humoral responses
10.3389/fimmu.2020.576743 · doi-reference
T cells expressing multiple co-inhibitory molecules in acute malaria are not exhausted but exert a suppressive function in mice
10.1002/eji.202149424 · doi-reference
Upregulation of LAG3 modulates the immune imbalance of CD4+ T-cell subsets and exacerbates disease progression in patients with alveolar echinococcosis and a mouse model
10.1371/journal.ppat.1011396 · doi-reference
Blockade of Tim-3 pathway in a mouse model of toxoplasmosis: impact on brain leukocyte infiltration, parasite burden, and neuroinflammation
10.1038/s41598-026-49283-8 · doi-reference
The expression of PD-1 and its ligands increases in Leishmania infection and its blockade reduces the parasite burden
10.1016/j.cyto.2022.155839 · doi-reference
Role of the PD-1/PD-L1 pathway in experimental Trypanosoma cruzi infection and potential therapeutic options
10.3389/fimmu.2022.866120 · doi-reference
Immune exhaustion of T cells in alveolar echinococcosis patients and its reversal by blocking checkpoint receptor TIGIT in a murine model
10.1002/hep.30896 · doi-reference
The expression of CTLA-4 in hepatic alveolar echinococcosis patients and blocking CTLA-4 to reverse T cell exhaustion in Echinococcus multilocularis-infected mice
10.3389/fimmu.2024.1358361 · doi-reference
Proliferation of MDSCs may indicate a lower CD4+ T cell immune response in schistosomiasis japonica. La prolifération des MDSC peut indiquer une réponse immunitaire des lymphocytes T CD4+ plus faible dans la schistosomiase japonica
10.1051/parasite/2024050 · doi-reference
IRF4 regulates myeloid-derived suppressor cells expansion and function in Schistosoma japonicum-infected mice
10.1186/s13071-024-06543-8 · doi-reference
Myeloid-derived suppressor cells (MDSCs) in the tumor microenvironment and their targeting in cancer therapy
10.1186/s12943-024-02208-3 · doi-reference
Emerging role of MDSCs as novel biomarkers and therapeutic targets for cancer immunotherapy
10.2147/itt.s485642 · doi-reference
Ex vivo generation of myeloid-derived suppressor cells that model the tumor immunosuppressive environment in colorectal cancer
10.18632/oncotarget.3682 · doi-reference
Myeloid-derived suppressor cells: The expanding world of helminth modulation of the immune system
10.3389/fimmu.2022.874308 · doi-reference
A Schistosoma japonicum infection promotes the expansion of myeloid-derived suppressor cells by activating the JAK/STAT3 pathway
10.4049/jimmunol.1601860 · doi-reference
History of myeloid-derived suppressor cells
10.1038/nrc3581 · doi-reference
Evolution of our understanding of myeloid regulatory cells: From MDSCs to Mregs
10.3389/fimmu.2014.00303 · doi-reference
LCMV-mediated loss of virtual memory CD8 T cells yields a functionally enhanced T cell subset
10.1016/j.isci.2025.113893 · doi-reference
IL-4 induces CD22 expression to restrain the effector program of virtual memory T cells
10.1126/sciimmunol.adk4841 · doi-reference
UFL1 promotes survival and function of virtual memory CD8 T cells
10.1093/jimmun/vkae042 · doi-reference
Helminth-induced IL-4 expands bystander memory CD8+ T cells for early control of viral infection
10.1038/s41467-018-06978-5 · doi-reference
Virtual memory CD8 T cells expanded by helminth infection confer broad protection against bacterial infection
10.1038/s41385-018-0100-x · doi-reference
Roles of virtual memory T cells in diseases
10.4110/in.2023.23.e11 · doi-reference
Similar but different: Virtual memory CD8 T cells as a memory-like cell population
10.1111/imcb.12277 · doi-reference
Virtual memory CD8+ T cells: Origin and beyond
10.1089/jir.2022.0053 · doi-reference
