<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Eichmann M</submitter><funding>NIDDK NIH HHS</funding><funding>National Institute for Health Research (NIHR)</funding><funding>National Institutes of Health</funding><pagination>3129-3138</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7378361</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>204(12)</volume><pubmed_abstract>We previously reported that costimulation blockade by abatacept limits the decline of β-cell function and the frequency of circulating CD4&lt;sup>+&lt;/sup> central memory T cells (T&lt;sub>CM&lt;/sub>) (CD45RO&lt;sup>+&lt;/sup>CD62L&lt;sup>+&lt;/sup>) in new-onset type 1 diabetes. In human subjects receiving placebo, we found a significant association between an increase in CD4&lt;sup>+&lt;/sup> T&lt;sub>CM&lt;/sub> cells and the decline of β-cell function. To extend and refine these findings, we examined changes in human CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> naive and memory T cell subsets at greater resolution using polychromatic flow and mass cytometry. In the placebo group, we successfully reproduced the original finding of a significant association between T&lt;sub>CM&lt;/sub> and β-cell function and extended this to other T c</pubmed_abstract><journal>Journal of immunology (Baltimore, Md. : 1950)</journal><pubmed_title>Costimulation Blockade Disrupts CD4&lt;sup>+&lt;/sup> T Cell Memory Pathways and Uncouples Their Link to Decline in β-Cell Function in Type 1 Diabetes.</pubmed_title><pmcid>PMC7378361</pmcid><funding_grant_id>U01 DK085461</funding_grant_id><funding_grant_id>U01 DK061010</funding_grant_id><funding_grant_id>U01 DK061042</funding_grant_id><funding_grant_id>U01 DK061034</funding_grant_id><funding_grant_id>U01 DK085476</funding_grant_id><funding_grant_id>U01 DK085465</funding_grant_id><funding_grant_id>DP3DK101109</funding_grant_id><funding_grant_id>U01 DK085466</funding_grant_id><funding_grant_id>U01 DK085499</funding_grant_id><funding_grant_id>U01 DK061058</funding_grant_id><funding_grant_id>U01 DK103180</funding_grant_id><funding_grant_id>U01 DK085509</funding_grant_id><funding_grant_id>UC4 DK106993</funding_grant_id><funding_grant_id>U01 DK107013</funding_grant_id><funding_grant_id>U01 DK107014</funding_grant_id><funding_grant_id>U01 DK106994</funding_grant_id><funding_grant_id>U01 DK106984</funding_grant_id><funding_grant_id>U01 DK103266</funding_grant_id><funding_grant_id>U01 DK103153</funding_grant_id><funding_grant_id>DP3 DK101109</funding_grant_id><funding_grant_id>U01 DK103282</funding_grant_id><pubmed_authors>Ellis RJ</pubmed_authors><pubmed_authors>Heck S</pubmed_authors><pubmed_authors>Peakman M</pubmed_authors><pubmed_authors>Beam CA</pubmed_authors><pubmed_authors>Baptista R</pubmed_authors><pubmed_authors>Eichmann M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Costimulation Blockade Disrupts CD4&lt;sup>+&lt;/sup> T Cell Memory Pathways and Uncouples Their Link to Decline in β-Cell Function in Type 1 Diabetes.</name><description>We previously reported that costimulation blockade by abatacept limits the decline of β-cell function and the frequency of circulating CD4&lt;sup>+&lt;/sup> central memory T cells (T&lt;sub>CM&lt;/sub>) (CD45RO&lt;sup>+&lt;/sup>CD62L&lt;sup>+&lt;/sup>) in new-onset type 1 diabetes. In human subjects receiving placebo, we found a significant association between an increase in CD4&lt;sup>+&lt;/sup> T&lt;sub>CM&lt;/sub> cells and the decline of β-cell function. To extend and refine these findings, we examined changes in human CD4&lt;sup>+&lt;/sup> and CD8&lt;sup>+&lt;/sup> naive and memory T cell subsets at greater resolution using polychromatic flow and mass cytometry. In the placebo group, we successfully reproduced the original finding of a significant association between T&lt;sub>CM&lt;/sub> and β-cell function and extended this to other T c</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2026-05-02T16:44:10.879Z</modification><creation>2022-02-10T14:49:13.384Z</creation></dates><accession>S-EPMC7378361</accession><cross_references><pubmed>32404353</pubmed><doi>10.4049/jimmunol.1901439</doi></cross_references></HashMap>