<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu K</submitter><funding>NIDA NIH HHS</funding><pagination>e70267</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11896887</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The HIV-1 reservoir in CD4+ T cells (HR&lt;sub>CD4&lt;/sub>) pose a major challenge to curing HIV, with many of its mechanisms still unclear. HIV-1 DNA integration and immune responses may alter the host's epigenetic landscape, potentially silencing HIV-1 replication.&lt;h4>Methods&lt;/h4>This study used bisulphite capture DNA methylation sequencing in CD4+ T cells from the blood of 427 virally suppressed women with HIV to identify differentially methylated sites and regions associated with HR&lt;sub>CD4&lt;/sub>.&lt;h4>Results&lt;/h4>The average total HR&lt;sub>CD4&lt;/sub> size was 1409 copies per million cells, with most proviruses defective and only a small proportion intact. The study identified 245 differentially methylated CpG sites and 85 regions linked to HR&lt;sub>CD4&lt;/sub> size, with 52% of s</pubmed_abstract><journal>Clinical and translational medicine</journal><pubmed_title>Aberrant DNA methylation of genes regulating CD4+ T cell HIV-1 reservoir in women with HIV.</pubmed_title><pmcid>PMC11896887</pmcid><funding_grant_id>R01DA047820</funding_grant_id><funding_grant_id>R01DA052846</funding_grant_id><funding_grant_id>R01DA047063</funding_grant_id><funding_grant_id>R01DA061926</funding_grant_id><pubmed_authors>Xu K</pubmed_authors><pubmed_authors>Asam K</pubmed_authors><pubmed_authors>Kuniholm MH</pubmed_authors><pubmed_authors>Archin NM</pubmed_authors><pubmed_authors>Page GP</pubmed_authors><pubmed_authors>Valizadeh A</pubmed_authors><pubmed_authors>Topper EF</pubmed_authors><pubmed_authors>Cohen MH</pubmed_authors><pubmed_authors>Aouizerat BE</pubmed_authors><pubmed_authors>DeHovitz J</pubmed_authors><pubmed_authors>Tien PC</pubmed_authors><pubmed_authors>Marconi VC</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Johnson EO</pubmed_authors><pubmed_authors>Lahiri CD</pubmed_authors><pubmed_authors>Martinez C</pubmed_authors><pubmed_authors>Hancock DB</pubmed_authors><pubmed_authors>Konkle-Parker D</pubmed_authors><pubmed_authors>Quach BC</pubmed_authors><pubmed_authors>Kassaye SG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aberrant DNA methylation of genes regulating CD4+ T cell HIV-1 reservoir in women with HIV.</name><description>&lt;h4>Background&lt;/h4>The HIV-1 reservoir in CD4+ T cells (HR&lt;sub>CD4&lt;/sub>) pose a major challenge to curing HIV, with many of its mechanisms still unclear. HIV-1 DNA integration and immune responses may alter the host's epigenetic landscape, potentially silencing HIV-1 replication.&lt;h4>Methods&lt;/h4>This study used bisulphite capture DNA methylation sequencing in CD4+ T cells from the blood of 427 virally suppressed women with HIV to identify differentially methylated sites and regions associated with HR&lt;sub>CD4&lt;/sub>.&lt;h4>Results&lt;/h4>The average total HR&lt;sub>CD4&lt;/sub> size was 1409 copies per million cells, with most proviruses defective and only a small proportion intact. The study identified 245 differentially methylated CpG sites and 85 regions linked to HR&lt;sub>CD4&lt;/sub> size, with 52% of s</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-04-04T01:41:24.005Z</modification><creation>2025-04-04T01:41:24.005Z</creation></dates><accession>S-EPMC11896887</accession><cross_references><pubmed>40070009</pubmed><doi>10.1002/ctm2.70267</doi></cross_references></HashMap>