<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fogle JE</submitter><funding>NIAID NIH HHS</funding><pagination>97</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2997086</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Using the FIV model, we reported previously that CD4+CD25+ T regulatory (Treg) cells from FIV+ cats are constitutively activated and suppress CD4+CD25- and CD8+ T cell immune responses. In an effort to further explore Treg-mediated suppression, we asked whether Treg cells induce anergy through the alteration of production of cyclins, cyclin-dependent kinases and their inhibitors.&lt;h4>Results&lt;/h4>Lymphocytes were obtained from control or FIV+ cats and sorted by FACS into CD4+CD25+ and CD8+ populations. Following co-culture with CD4+CD25+ cells, CD8+ targets were examined by Western blot for changes in cyclins D3, E and A, retinoblastoma (Rb) protein, as well as the cyclin dependent kinase inhibitor p21cip1. Following co-culture with CD4+CD25+cells, we observed up-regulatio</pubmed_abstract><journal>Retrovirology</journal><pubmed_title>CD4+CD25+ T regulatory cells from FIV+ cats induce a unique anergic profile in CD8+ lymphocyte targets.</pubmed_title><pmcid>PMC2997086</pmcid><funding_grant_id>R01 AI080288</funding_grant_id><funding_grant_id>AI080288</funding_grant_id><funding_grant_id>1K08AI074445</funding_grant_id><pubmed_authors>Tompkins MB</pubmed_authors><pubmed_authors>Fogle JE</pubmed_authors><pubmed_authors>Tompkins WA</pubmed_authors></additional><is_claimable>false</is_claimable><name>CD4+CD25+ T regulatory cells from FIV+ cats induce a unique anergic profile in CD8+ lymphocyte targets.</name><description>&lt;h4>Background&lt;/h4>Using the FIV model, we reported previously that CD4+CD25+ T regulatory (Treg) cells from FIV+ cats are constitutively activated and suppress CD4+CD25- and CD8+ T cell immune responses. In an effort to further explore Treg-mediated suppression, we asked whether Treg cells induce anergy through the alteration of production of cyclins, cyclin-dependent kinases and their inhibitors.&lt;h4>Results&lt;/h4>Lymphocytes were obtained from control or FIV+ cats and sorted by FACS into CD4+CD25+ and CD8+ populations. Following co-culture with CD4+CD25+ cells, CD8+ targets were examined by Western blot for changes in cyclins D3, E and A, retinoblastoma (Rb) protein, as well as the cyclin dependent kinase inhibitor p21cip1. Following co-culture with CD4+CD25+cells, we observed up-regulatio</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Nov</publication><modification>2025-04-18T16:35:41.917Z</modification><creation>2019-03-27T00:37:11Z</creation></dates><accession>S-EPMC2997086</accession><cross_references><pubmed>21092106</pubmed><doi>10.1186/1742-4690-7-97</doi></cross_references></HashMap>