Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/20873
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dc.contributor.authorOGUNJIMI, Benson-
dc.contributor.authorHENS, Niel-
dc.contributor.authorPebody, R.-
dc.contributor.authorJansens, H.-
dc.contributor.authorSeale, H.-
dc.contributor.authorQuinlivan, M.-
dc.contributor.authorTheeten, H.-
dc.contributor.authorGoossens, Herman-
dc.contributor.authorBreuer, Judy-
dc.contributor.authorBeutels, Philippe-
dc.date.accessioned2016-03-31T15:18:36Z-
dc.date.available2016-03-31T15:18:36Z-
dc.date.issued2015-
dc.identifier.citationHuman Vaccines & Immunotherapeutics 11(6), p. 1394-1399-
dc.identifier.issn2164-5515-
dc.identifier.urihttp://hdl.handle.net/1942/20873-
dc.description.abstractHerpes zoster (HZ) is caused by VZV reactivation that is facilitated by a declined immunity against varicella-zoster virus (VZV), but also occurs in immunocompetent individuals. Cytomegalovirus (CMV) infection is associated with immunosenescence meaning that VZV-specific T-cells could be less responsive. This study aimed to determine whether CMV infection could be a risk factor for the development of HZ. CMV IgG serostatus was determined in stored serum samples from previously prospectively recruited ambulatory adult HZ patients in the UK (N D 223) in order to compare the results with those from UK population samples (N D 1545) by means of a logistic regression (controlling for age and gender). Furthermore, we compared the UK population CMV seroprevalence with those from population samples from other countries (from Belgium (N1 D 1741, N2 D 576), USA (N D 5572) and Australia (N D 2080)). Furthermore, CMV IgG titers could be compared between UK HZ patients and Belgium N2 population samples because the same experimental set-up for analysis was used. We found UK ambulatory HZ patients to have a higher CMV seroprevalence than UK population samples (OR 1.56 [1.11 2.19]). CMV IgG seropositivity was a significant risk factor for HZ in the UK (OR 3.06 [1.32 7.04]. Furthermore, high CMV IgG titers (exceeding the upper threshold) were less abundant in CMV-seropositive Belgian N2 population samples than in CMV-seropositive UK HZ patients (OR 0.51 [0.31 0.82]. We found CMVseroprevalence to increase faster with age in the UK than in other countries (P < 0.05). We conclude that CMV IgG seropositivity is associated with HZ. This finding could add to the growing list of risk factors for HZ.-
dc.description.sponsorshipThis work was supported by the Research Foundation Flanders (FWO) [personal grants to B.O. and H.T. and project grant G040912N]; the University of Antwerp [Pfizer-sponsored scientific chair to N.H.]; The Wellcome Trust [081703/B/06/Z] and the National Institute for Health Research (NIHR) UCL/UCLH Comprehensive Biomedical Research Center [to J.B.].-
dc.language.isoen-
dc.rights© 2015 Taylor & Francis Group, LLC-
dc.subject.otherCMV; immunosenescence; reactivation; shingles; susceptibility; zoster-
dc.titleCytomegalovirus seropositivity is associated with herpes zoster-
dc.typeJournal Contribution-
dc.identifier.epage1399-
dc.identifier.issue6-
dc.identifier.spage1394-
dc.identifier.volume11-
local.bibliographicCitation.jcatA1-
dc.description.notesCorrespondence to: Benson Ogunjimi; Email: benson.ogunjimi@uantwerp.be-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1080/21645515.2015.1037999-
dc.identifier.isi000356426800026-
item.fulltextWith Fulltext-
item.contributorOGUNJIMI, Benson-
item.contributorHENS, Niel-
item.contributorPebody, R.-
item.contributorJansens, H.-
item.contributorSeale, H.-
item.contributorQuinlivan, M.-
item.contributorTheeten, H.-
item.contributorGoossens, Herman-
item.contributorBreuer, Judy-
item.contributorBeutels, Philippe-
item.fullcitationOGUNJIMI, Benson; HENS, Niel; Pebody, R.; Jansens, H.; Seale, H.; Quinlivan, M.; Theeten, H.; Goossens, Herman; Breuer, Judy & Beutels, Philippe (2015) Cytomegalovirus seropositivity is associated with herpes zoster. In: Human Vaccines & Immunotherapeutics 11(6), p. 1394-1399.-
item.accessRightsRestricted Access-
item.validationecoom 2016-
crisitem.journal.issn2164-5515-
crisitem.journal.eissn2164-554X-
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