<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Knox JJ</submitter><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>National Heart, Lung, and Blood Institute</funding><pagination>317-324</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11952879</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>214(3)</volume><pubmed_abstract>The humoral immune system influences the development of atherosclerosis, but the contributions of specific memory B cell subsets and IgG isotypes are poorly understood. We assessed the relationship between atherosclerosis and age-associated B cells (ABCs), a T-bet-expressing memory B cell subset that is enriched for IgG2c production and implicated in humoral autoimmunity. We found increased numbers of splenic CD11c+ ABCs in 6-mo-old, chow-fed Apoe-/- mice versus C57BL/6 control mice, which were exacerbated by high-fat diet. Deletion of T-bet in the B lineage in high-fat diet-fed Apoe-/- mice reduced aortic lesion area, and this correlated with decreased splenic CD11c+ B cells and reduced serum oxidized low-density lipoprotein-specific IgG2c. Our findings suggest that T-bet-expressing B cel</pubmed_abstract><journal>Journal of immunology (Baltimore, Md. : 1950)</journal><pubmed_title>T-bet-expressing B cells promote atherosclerosis in apolipoprotein E-deficient mice.</pubmed_title><pmcid>PMC11952879</pmcid><funding_grant_id>T32 AI055428</funding_grant_id><funding_grant_id>T32 HL007954</funding_grant_id><funding_grant_id>T32 HL07954</funding_grant_id><pubmed_authors>Rader DJ</pubmed_authors><pubmed_authors>Cancro MP</pubmed_authors><pubmed_authors>Cromley D</pubmed_authors><pubmed_authors>Pure E</pubmed_authors><pubmed_authors>Karolyi K</pubmed_authors><pubmed_authors>Knox JJ</pubmed_authors><pubmed_authors>Monslow J</pubmed_authors></additional><is_claimable>false</is_claimable><name>T-bet-expressing B cells promote atherosclerosis in apolipoprotein E-deficient mice.</name><description>The humoral immune system influences the development of atherosclerosis, but the contributions of specific memory B cell subsets and IgG isotypes are poorly understood. We assessed the relationship between atherosclerosis and age-associated B cells (ABCs), a T-bet-expressing memory B cell subset that is enriched for IgG2c production and implicated in humoral autoimmunity. We found increased numbers of splenic CD11c+ ABCs in 6-mo-old, chow-fed Apoe-/- mice versus C57BL/6 control mice, which were exacerbated by high-fat diet. Deletion of T-bet in the B lineage in high-fat diet-fed Apoe-/- mice reduced aortic lesion area, and this correlated with decreased splenic CD11c+ B cells and reduced serum oxidized low-density lipoprotein-specific IgG2c. Our findings suggest that T-bet-expressing B cel</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-07-16T23:07:35.397Z</modification><creation>2026-07-12T03:10:41.366Z</creation></dates><accession>S-EPMC11952879</accession><cross_references><pubmed>40073097</pubmed><doi>10.1093/jimmun/vkae027</doi></cross_references></HashMap>