<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Manandhar P</submitter><funding>HHS | NIH | National Cancer Institute</funding><funding>NIAID NIH HHS</funding><funding>HHS | NIH | NIAID | Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases</funding><funding>NCI NIH HHS</funding><pagination>466-474</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10906969</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>212(3)</volume><pubmed_abstract>Tim-3 is a transmembrane protein that is best known for being highly expressed on terminally exhausted CD8+ T cells associated with chronic infection and tumors, although its expression is not limited to those settings. Tim-3 is also expressed by CD8+ T cells during acute infection and by multiple other immune cell types, including CD4+ Th1 and regulatory T cells, dendritic cells, and mast cells. In this study, we investigated the role of Tim-3 signaling on CD8+ T cell memory using a Tim-3 conditional knockout mouse model and mice lacking the signaling portion of the Tim-3 cytoplasmic domain. Together, our results indicate that Tim-3 has at most a modest effect on the formation and function of CD8+ memory T cells.</pubmed_abstract><journal>Journal of immunology (Baltimore, Md. : 1950)</journal><pubmed_title>Tim-3 Is Not Required for Establishment of CD8+ T Cell Memory to Lymphocytic Choriomeningitis Virus.</pubmed_title><pmcid>PMC10906969</pmcid><funding_grant_id>T32 CA082084</funding_grant_id><funding_grant_id>R01 AI138504</funding_grant_id><funding_grant_id>R01 CA206517</funding_grant_id><funding_grant_id>R03 AI131049</funding_grant_id><pubmed_authors>Kane LP</pubmed_authors><pubmed_authors>Szymczak-Workman AL</pubmed_authors><pubmed_authors>Manandhar P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tim-3 Is Not Required for Establishment of CD8+ T Cell Memory to Lymphocytic Choriomeningitis Virus.</name><description>Tim-3 is a transmembrane protein that is best known for being highly expressed on terminally exhausted CD8+ T cells associated with chronic infection and tumors, although its expression is not limited to those settings. Tim-3 is also expressed by CD8+ T cells during acute infection and by multiple other immune cell types, including CD4+ Th1 and regulatory T cells, dendritic cells, and mast cells. In this study, we investigated the role of Tim-3 signaling on CD8+ T cell memory using a Tim-3 conditional knockout mouse model and mice lacking the signaling portion of the Tim-3 cytoplasmic domain. Together, our results indicate that Tim-3 has at most a modest effect on the formation and function of CD8+ memory T cells.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-05T10:18:54.128Z</modification><creation>2025-04-05T10:18:54.128Z</creation></dates><accession>S-EPMC10906969</accession><cross_references><pubmed>38108417</pubmed><doi>10.4049/jimmunol.2300401</doi></cross_references></HashMap>