<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Luo Q</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>CD4&lt;sup>+&lt;/sup>T cells are significant compositions of immune cells in rheumatoid arthritis (RA) and the aberrant function of CD4&lt;sup>+&lt;/sup>T cells have been demonstrated to promote RA's progression. N6-methyladenosine (m6A) is a highly enriched modification found in CircRNAs. However, the role of m6A-methylated circRNA in regulation of CD4&lt;sup>+&lt;/sup>T cells function in RA and its association with RA disease activity are presently unclear.&lt;h4>Methods&lt;/h4>We used m6A-circRNA epitranscriptomic microarray analysis and m6A RNA immunocoprecipitation-quantitative polymerase chain reaction (MeRIP-qPCR) to screen and verify the differentially expressed m6A-methylated circRNAs in CD4&lt;sup>+&lt;/sup>T cells from RA and HC.&lt;h4>Results&lt;/h4>Many m6A-methylated circRNAs were differential</pubmed_abstract><journal>Journal of translational autoimmunity</journal><pagination>100326</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12554200</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The significance of m6A-circFOXK2 in CD4&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;T cells from patients with rheumatoid arthritis and circFOXK2 correlates with Th17 % and autophagy.</pubmed_title><pmcid>PMC12554200</pmcid><pubmed_authors>Fu B</pubmed_authors><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Luo Q</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Huang Z</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Lan M</pubmed_authors><pubmed_authors>Fu P</pubmed_authors><pubmed_authors>Xiao Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>The significance of m6A-circFOXK2 in CD4&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;T cells from patients with rheumatoid arthritis and circFOXK2 correlates with Th17 % and autophagy.</name><description>&lt;h4>Objective&lt;/h4>CD4&lt;sup>+&lt;/sup>T cells are significant compositions of immune cells in rheumatoid arthritis (RA) and the aberrant function of CD4&lt;sup>+&lt;/sup>T cells have been demonstrated to promote RA's progression. N6-methyladenosine (m6A) is a highly enriched modification found in CircRNAs. However, the role of m6A-methylated circRNA in regulation of CD4&lt;sup>+&lt;/sup>T cells function in RA and its association with RA disease activity are presently unclear.&lt;h4>Methods&lt;/h4>We used m6A-circRNA epitranscriptomic microarray analysis and m6A RNA immunocoprecipitation-quantitative polymerase chain reaction (MeRIP-qPCR) to screen and verify the differentially expressed m6A-methylated circRNAs in CD4&lt;sup>+&lt;/sup>T cells from RA and HC.&lt;h4>Results&lt;/h4>Many m6A-methylated circRNAs were differential</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-04T03:08:09.661Z</modification><creation>2026-06-04T03:06:11.417Z</creation></dates><accession>S-EPMC12554200</accession><cross_references><pubmed>41146880</pubmed><doi>10.1016/j.jtauto.2025.100326</doi></cross_references></HashMap>