<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>61</viewCount><searchCount>0</searchCount></scores><additional><submitter>Bromley SK</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>NIAID NIH HHS</funding><pagination>108085</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7520726</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>32(9)</volume><pubmed_abstract>CD8&lt;sup>+&lt;/sup> tissue-resident memory T cells (T&lt;sub>RM&lt;/sub>) persist at sites of previous infection, where they provide rapid local protection against pathogen challenge. CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub> expressing the α1 chain (CD49a) of integrin VLA-1 have been identified within sites of resolved skin infection and in vitiligo lesions. We demonstrate that CD49a is expressed early following T cell activation in vivo, and TGF-β and IL-12 induce CD49a expression by CD8&lt;sup>+&lt;/sup> T cells in vitro. Despite this rapid expression, CD49a is not required for the generation of a primary CD8&lt;sup>+&lt;/sup> T cell response to cutaneous herpes simplex virus (HSV) infection, migration of CD8&lt;sup>+&lt;/sup> T cells across the epidermal basement membrane, or positioning of T&lt;sub>RM&lt;/sub> within basal epidermis. Rather, CD49a supports CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub> persistence within skin, regulates epidermal CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub> dendritic extensions, and increases the frequency of IFN-γ&lt;sup>+&lt;/sup> CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub> following local antigen challenge. Our results suggest that CD49a promotes optimal cutaneous CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub>-mediated immunity.</pubmed_abstract><journal>Cell reports</journal><pubmed_title>CD49a Regulates Cutaneous Resident Memory CD8&lt;sup>+&lt;/sup> T Cell Persistence and Response.</pubmed_title><pmcid>PMC7520726</pmcid><funding_grant_id>R01 AI121546</funding_grant_id><funding_grant_id>R01 AI040618</funding_grant_id><pubmed_authors>Luster AD</pubmed_authors><pubmed_authors>Bromley SK</pubmed_authors><pubmed_authors>Mora-Buch R</pubmed_authors><pubmed_authors>Akbaba H</pubmed_authors><pubmed_authors>Mani V</pubmed_authors><pubmed_authors>Chasse AY</pubmed_authors><pubmed_authors>Sama A</pubmed_authors><view_count>61</view_count></additional><is_claimable>false</is_claimable><name>CD49a Regulates Cutaneous Resident Memory CD8&lt;sup>+&lt;/sup> T Cell Persistence and Response.</name><description>CD8&lt;sup>+&lt;/sup> tissue-resident memory T cells (T&lt;sub>RM&lt;/sub>) persist at sites of previous infection, where they provide rapid local protection against pathogen challenge. CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub> expressing the α1 chain (CD49a) of integrin VLA-1 have been identified within sites of resolved skin infection and in vitiligo lesions. We demonstrate that CD49a is expressed early following T cell activation in vivo, and TGF-β and IL-12 induce CD49a expression by CD8&lt;sup>+&lt;/sup> T cells in vitro. Despite this rapid expression, CD49a is not required for the generation of a primary CD8&lt;sup>+&lt;/sup> T cell response to cutaneous herpes simplex virus (HSV) infection, migration of CD8&lt;sup>+&lt;/sup> T cells across the epidermal basement membrane, or positioning of T&lt;sub>RM&lt;/sub> within basal epidermis. Rather, CD49a supports CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub> persistence within skin, regulates epidermal CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub> dendritic extensions, and increases the frequency of IFN-γ&lt;sup>+&lt;/sup> CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub> following local antigen challenge. Our results suggest that CD49a promotes optimal cutaneous CD8&lt;sup>+&lt;/sup> T&lt;sub>RM&lt;/sub>-mediated immunity.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2024-11-08T17:47:25.893Z</modification><creation>2020-10-08T07:20:37Z</creation></dates><accession>S-EPMC7520726</accession><cross_references><pubmed>32877667</pubmed><doi>10.1016/j.celrep.2020.108085</doi></cross_references></HashMap>