<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Misumi I</submitter><funding>NIDDK NIH HHS</funding><funding>NCI</funding><funding>NIAID NIH HHS</funding><funding>Pilot &amp;amp; Feasibility</funding><funding>Nutrition Obesity Research Center</funding><funding>NCI NIH HHS</funding><funding>NIH</funding><funding>UNC-CH</funding><pagination>514-524.e5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6652206</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(2)</volume><pubmed_abstract>Obesity in humans is associated with poorer health outcomes after infections compared with non-obese individuals. Here, we examined the effects of white adipose tissue and obesity on T cell responses to viral infection in mice. We show that lymphocytic choriomeningitis virus (LCMV) grows to high titer in adipose tissue. Virus-specific T cells enter the adipose tissue to resolve infection but then remain as a memory population distinct from memory T cells in lymphoid tissues. Memory T cells in adipose tissue are abundant in lean mice, and diet-induced obesity further increases memory T cell number in adipose tissue and spleen. Upon re-challenge infection, memory T cells rapidly cause severe pathogenesis, leading to increases in lipase levels, calcification of adipose tissue, pancreatitis, a</pubmed_abstract><journal>Cell reports</journal><pubmed_title>Obesity Expands a Distinct Population of T Cells in Adipose Tissue and Increases Vulnerability to Infection.</pubmed_title><pmcid>PMC6652206</pmcid><funding_grant_id>R56 AI110682</funding_grant_id><funding_grant_id>P30 DK056350</funding_grant_id><funding_grant_id>P30CA016086</funding_grant_id><funding_grant_id>P30 CA016086</funding_grant_id><funding_grant_id>R01AI138337</funding_grant_id><funding_grant_id>R56AI110682</funding_grant_id><funding_grant_id>R01 AI138337</funding_grant_id><funding_grant_id>R21 AI117575</funding_grant_id><funding_grant_id>R21AI117575</funding_grant_id><funding_grant_id>R01-GM10974</funding_grant_id><funding_grant_id>P30DK56350</funding_grant_id><pubmed_authors>Beck MA</pubmed_authors><pubmed_authors>Uchimura T</pubmed_authors><pubmed_authors>Magnuson T</pubmed_authors><pubmed_authors>Whitmire JK</pubmed_authors><pubmed_authors>Misumi I</pubmed_authors><pubmed_authors>Starmer J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Obesity Expands a Distinct Population of T Cells in Adipose Tissue and Increases Vulnerability to Infection.</name><description>Obesity in humans is associated with poorer health outcomes after infections compared with non-obese individuals. Here, we examined the effects of white adipose tissue and obesity on T cell responses to viral infection in mice. We show that lymphocytic choriomeningitis virus (LCMV) grows to high titer in adipose tissue. Virus-specific T cells enter the adipose tissue to resolve infection but then remain as a memory population distinct from memory T cells in lymphoid tissues. Memory T cells in adipose tissue are abundant in lean mice, and diet-induced obesity further increases memory T cell number in adipose tissue and spleen. Upon re-challenge infection, memory T cells rapidly cause severe pathogenesis, leading to increases in lipase levels, calcification of adipose tissue, pancreatitis, a</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Apr</publication><modification>2026-05-07T05:16:28.121Z</modification><creation>2019-07-30T07:09:19Z</creation></dates><accession>S-EPMC6652206</accession><cross_references><pubmed>30970254</pubmed><doi>10.1016/j.celrep.2019.03.030</doi></cross_references></HashMap>