<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hassan N</submitter><funding>Cancer Research UK</funding><funding>Medical Research Council</funding><funding>Blood Cancer UK</funding><funding>National Institute for Health Research (NIHR)</funding><pagination>935949</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9753568</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>NK cells play an important role in suppression of viral replication and are critical for effective control of persistent infections such as herpesviruses. Cytomegalovirus infection is associated with expansion of 'adaptive-memory' NK cells with a characteristic CD56dimCD16bright NKG2C+ phenotype but the mechanisms by which this population is maintained remain uncertain.&lt;h4>Methods&lt;/h4>We studied NK cell reconstitution in patients undergoing haemopoietic stem cell transplantation and related this to CMV reactivation.&lt;h4>Results&lt;/h4>NK cells expanded in the early post-transplant period but then remained stable in the absence of viral reactivation. However, CMV reactivation led to a rapid and sustained 10-fold increase in NK cell number. The proportion of NKG2C-expressing</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>CMV reactivation initiates long-term expansion and differentiation of the NK cell repertoire.</pubmed_title><pmcid>PMC9753568</pmcid><funding_grant_id>29430</funding_grant_id><funding_grant_id>12052</funding_grant_id><funding_grant_id>CL-2015-09-001</funding_grant_id><funding_grant_id>NF-SI-0617-10163</funding_grant_id><funding_grant_id>MR/R011230/1</funding_grant_id><pubmed_authors>Hassan N</pubmed_authors><pubmed_authors>Kinsella F</pubmed_authors><pubmed_authors>Eldershaw S</pubmed_authors><pubmed_authors>Zuo J</pubmed_authors><pubmed_authors>Moss P</pubmed_authors><pubmed_authors>Craddock C</pubmed_authors><pubmed_authors>Stephens C</pubmed_authors><pubmed_authors>Malladi R</pubmed_authors></additional><is_claimable>false</is_claimable><name>CMV reactivation initiates long-term expansion and differentiation of the NK cell repertoire.</name><description>&lt;h4>Introduction&lt;/h4>NK cells play an important role in suppression of viral replication and are critical for effective control of persistent infections such as herpesviruses. Cytomegalovirus infection is associated with expansion of 'adaptive-memory' NK cells with a characteristic CD56dimCD16bright NKG2C+ phenotype but the mechanisms by which this population is maintained remain uncertain.&lt;h4>Methods&lt;/h4>We studied NK cell reconstitution in patients undergoing haemopoietic stem cell transplantation and related this to CMV reactivation.&lt;h4>Results&lt;/h4>NK cells expanded in the early post-transplant period but then remained stable in the absence of viral reactivation. However, CMV reactivation led to a rapid and sustained 10-fold increase in NK cell number. The proportion of NKG2C-expressing</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-07-14T16:04:00.378Z</modification><creation>2025-04-04T19:49:31.834Z</creation></dates><accession>S-EPMC9753568</accession><cross_references><pubmed>36531994</pubmed><doi>10.3389/fimmu.2022.935949</doi></cross_references></HashMap>