<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sun Y</submitter><funding>NIAID NIH HHS</funding><pagination>1542531</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11868092</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Cytomegalovirus (CMV) viremia remains a major contributor to clinical complications in solid organ transplant (SOT) patients, including organ injury, morbidity and mortality. Given their critical role in antiviral defense, CD8+ T cells are essential for protective immunity against CMV.&lt;h4>Methods&lt;/h4>Using single-cell RNA sequencing, we investigated the transcriptional signatures and developmental lineages of CD8+ T cells in eight immunosuppressed kidney transplant recipients (KTRs) who received organs from CMV-seropositive donors. Results were validated in a cohort of 62 KTRs using immunophenotyping.&lt;h4>Results&lt;/h4>Our data revealed a significant influence of CMV serostatus on transcriptional variance of CD8+ memory T cells, associating with the first principal compon</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Cytotoxic KLRG1+ IL-7R- effector CD8+ T cells distinguish kidney transplant recipients controlling cytomegalovirus reactivation.</pubmed_title><pmcid>PMC11868092</pmcid><funding_grant_id>U19 AI128913</funding_grant_id><pubmed_authors>Schaenman JM</pubmed_authors><pubmed_authors>Sarwal MM</pubmed_authors><pubmed_authors>Lanier LL</pubmed_authors><pubmed_authors>Cappelletti M</pubmed_authors><pubmed_authors>Arakawa-Hoyt J</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Sen S</pubmed_authors><pubmed_authors>Sigdel TK</pubmed_authors><pubmed_authors>Rossetti M</pubmed_authors><pubmed_authors>Bunnapradist S</pubmed_authors><pubmed_authors>Pickering H</pubmed_authors><pubmed_authors>Reed EF</pubmed_authors><pubmed_authors>Gjertson DW</pubmed_authors><pubmed_authors>Parmar R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cytotoxic KLRG1+ IL-7R- effector CD8+ T cells distinguish kidney transplant recipients controlling cytomegalovirus reactivation.</name><description>&lt;h4>Introduction&lt;/h4>Cytomegalovirus (CMV) viremia remains a major contributor to clinical complications in solid organ transplant (SOT) patients, including organ injury, morbidity and mortality. Given their critical role in antiviral defense, CD8+ T cells are essential for protective immunity against CMV.&lt;h4>Methods&lt;/h4>Using single-cell RNA sequencing, we investigated the transcriptional signatures and developmental lineages of CD8+ T cells in eight immunosuppressed kidney transplant recipients (KTRs) who received organs from CMV-seropositive donors. Results were validated in a cohort of 62 KTRs using immunophenotyping.&lt;h4>Results&lt;/h4>Our data revealed a significant influence of CMV serostatus on transcriptional variance of CD8+ memory T cells, associating with the first principal compon</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2025-04-03T23:36:46.17Z</modification><creation>2025-04-03T23:36:46.17Z</creation></dates><accession>S-EPMC11868092</accession><cross_references><pubmed>40028342</pubmed><doi>10.3389/fimmu.2025.1542531</doi></cross_references></HashMap>