<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>30(3)</volume><submitter>Huang S</submitter><pubmed_abstract>Immunosuppression in response to severe sepsis remains a serious human health concern. Evidence of sepsis-induced immunosuppression includes impaired T lymphocyte function, T lymphocyte depletion or exhaustion, increased susceptibility to opportunistic nosocomial infection, and imbalanced cytokine secretion. CD4 T cells play a critical role in cellular and humoral immune responses during sepsis. Here, using an RNA sequencing assay, we found that the expression of T cell-containing immunoglobulin and mucin domain-3 (Tim-3) on CD4 T cells in sepsis-induced immunosuppression patients was significantly elevated. Furthermore, the percentage of Tim-3&lt;sup>+&lt;/sup> CD4 T cells from sepsis patients was correlated with the mortality of sepsis-induced immunosuppression. Conditional deletion of Tim-3 i</pubmed_abstract><journal>Molecular therapy : the journal of the American Society of Gene Therapy</journal><pagination>1227-1238</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8899604</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tim-3 regulates sepsis-induced immunosuppression by inhibiting the NF-κB signaling pathway in CD4 T cells.</pubmed_title><pmcid>PMC8899604</pmcid><pubmed_authors>Qiu J</pubmed_authors><pubmed_authors>Jiang J</pubmed_authors><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Gan L</pubmed_authors><pubmed_authors>Zeng L</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Deng J</pubmed_authors><pubmed_authors>Liu D</pubmed_authors><pubmed_authors>Qu G</pubmed_authors><pubmed_authors>Sun J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tim-3 regulates sepsis-induced immunosuppression by inhibiting the NF-κB signaling pathway in CD4 T cells.</name><description>Immunosuppression in response to severe sepsis remains a serious human health concern. Evidence of sepsis-induced immunosuppression includes impaired T lymphocyte function, T lymphocyte depletion or exhaustion, increased susceptibility to opportunistic nosocomial infection, and imbalanced cytokine secretion. CD4 T cells play a critical role in cellular and humoral immune responses during sepsis. Here, using an RNA sequencing assay, we found that the expression of T cell-containing immunoglobulin and mucin domain-3 (Tim-3) on CD4 T cells in sepsis-induced immunosuppression patients was significantly elevated. Furthermore, the percentage of Tim-3&lt;sup>+&lt;/sup> CD4 T cells from sepsis patients was correlated with the mortality of sepsis-induced immunosuppression. Conditional deletion of Tim-3 i</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-05-28T08:07:38.819Z</modification><creation>2025-04-25T17:05:38.374Z</creation></dates><accession>S-EPMC8899604</accession><cross_references><pubmed>34933101</pubmed><doi>10.1016/j.ymthe.2021.12.013</doi></cross_references></HashMap>