{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,27]],"date-time":"2026-09-27T12:10:26Z","timestamp":1790511026740,"version":"4.1.0"},"reference-count":56,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2018,10,5]],"date-time":"2018-10-05T00:00:00Z","timestamp":1538697600000},"content-version":"vor","delay-in-days":277,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/100004334","name":"Merck","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100004334","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clin &amp;amp; Trans Imm"],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Objectives<\/jats:title><jats:p>Infections are a major cause of mortality after allogeneic haemopoietic stem cell transplantation (allo<jats:styled-content style=\"fixed-case\">HSCT<\/jats:styled-content>), and immune recovery is necessary for prevention. Novel transplant procedures have changed the epidemiology of infections but contemporary data on functional immune recovery are limited. In this pilot study, we aimed to measure immune recovery in the current era of allo<jats:styled-content style=\"fixed-case\">HSCT<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Twenty, 13, 11, 9 and 9 allo<jats:styled-content style=\"fixed-case\">HSCT<\/jats:styled-content> recipients had blood collected at baseline (time of conditioning) and 3\u2010, 6\u2010, 9\u2010, and 12\u2010months post\u2010allo<jats:styled-content style=\"fixed-case\">HSCT<\/jats:styled-content>, respectively. Clinical data were collected, and immune recovery was measured using immunophenotyping, lymphocyte proliferation, cytokine analysis and antibody isotyping.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Median absolute T\u2010 and B\u2010cell counts were below normal from baseline until 9\u2010 to 12\u2010months post\u2010allo<jats:styled-content style=\"fixed-case\">HSCT<\/jats:styled-content>. Median absolute <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> T\u2010cell counts recovered at 12\u2010months post\u2010allo<jats:styled-content style=\"fixed-case\">HSCT<\/jats:styled-content>. Positive proliferative responses to <jats:italic>Aspergillus<\/jats:italic>, cytomegalovirus (<jats:styled-content style=\"fixed-case\">CMV<\/jats:styled-content>), Epstein\u2010Barr virus (<jats:styled-content style=\"fixed-case\">EBV<\/jats:styled-content>), influenza and tetanus antigens were detected from 9\u00a0months. <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20106 was the most abundant cytokine in cell cultures. In cultures stimulated with <jats:styled-content style=\"fixed-case\">CMV<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> EBV<\/jats:styled-content>, influenza and tetanus peptides, the <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> T\u2010cell count correlated with <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2 (<jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.045) and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> T\u2010cell count with <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\u03b3 (<jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.013) and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2 (<jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.012). The <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content>\u2010cell count correlated with <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2 (<jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.02) and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201017a (<jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.03). Median serum levels of IgG1, IgG2 and IgG3 were normal while IgG4 and IgA were below normal range throughout follow\u2010up.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>This pilot study demonstrates that immune recovery can be measured using <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> T\u2010cell counts, <jats:italic>in\u00a0vitro<\/jats:italic> antigen stimulation and selected cytokines (<jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\u03b3, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20104, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20106, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201017, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201021, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201031) in allo<jats:styled-content style=\"fixed-case\">HSCT<\/jats:styled-content> recipients. While larger studies are required, monitoring immune recovery may have utility in predicting infection risk post\u2010allo<jats:styled-content style=\"fixed-case\">HSCT<\/jats:styled-content>.<\/jats:p><\/jats:sec>","DOI":"10.1002\/cti2.1040","type":"journal-article","created":{"date-parts":[[2018,10,6]],"date-time":"2018-10-06T09:46:44Z","timestamp":1538819204000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":7,"title":["Contemporary analysis of functional immune recovery to opportunistic and vaccine\u2010preventable infections after allogeneic haemopoietic stem cell transplantation"],"prefix":"10.1002","volume":"7","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8062-0522","authenticated-orcid":false,"given":"Harini D","family":"de Silva","sequence":"first","affiliation":[{"name":"Burnet Institute Life Sciences Discipline Melbourne VIC Australia"},{"name":"Department of Infectious Diseases Alfred Health and Monash 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