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dc.contributor.authorWatanabe, Mizukien
dc.contributor.authorKanda, Junyaen
dc.contributor.authorHishizawa, Masakatsuen
dc.contributor.authorKondo, Tadakazuen
dc.contributor.authorYamashita, Kouheien
dc.contributor.authorTakaori-Kondo, Akifumien
dc.contributor.alternative諫⽥, 淳也ja
dc.contributor.alternative菱澤, 方勝ja
dc.contributor.alternative近藤, 忠一ja
dc.contributor.alternative山下, 浩平ja
dc.contributor.alternative髙折, 晃史ja
dc.date.accessioned2019-05-24T05:31:35Z-
dc.date.available2019-05-24T05:31:35Z-
dc.date.issued2019-03-
dc.identifier.issn1083-8791-
dc.identifier.issn1523-6536-
dc.identifier.urihttp://hdl.handle.net/2433/241617-
dc.description.abstractViral infection is a serious complication that can greatly affect patient mortality and morbidity after allogenic hematopoietic stem cell transplantation (allo-HSCT). For the early identification of patients at high risk for viral infection, we evaluated the impact of lymphocyte area under the curve (AUC) value as a new predictive factor for early immune reconstitution after allo-HSCT against viral infection. This study included 286 patients who underwent their first allo-HSCT at Kyoto University Hospital between 2005 and 2017. Lymphocyte AUC from day 0 to day +15 was calculated in the analysis of human herpesvirus 6 (HHV-6), and lymphocyte AUC from day 0 to day +30 was calculated in the analysis of other viruses (cytomegalovirus [CMV], adenovirus, BK virus, JC virus, and varicella zoster virus). The risk factors for each viral reactivation/infection were assessed by multivariate analysis. The median age at transplantation was 51 years (range, 17 to 68 years). The median lymphocyte AUC was 63/μL (range, 0 to 5620/μL) at day +15 and 3880 (range, 0 to 118, 260/μL) at day +30. An increase in lymphocyte AUC was significantly associated with a high frequency of HHV-6 reactivation (P = .033) and a low frequency of CMV antigenemia (P = .014). No apparent association was found between lymphocyte AUC and reactivation/infection of other viruses. Aplastic anemia as a primary disease (hazard ratio [HR], 5.34; P < .001) and cord blood as a donor source (HR, 3.05; P = .006) were other risk factors for HHV-6 reactivation. Other risk factors for CMV antigenemia included the occurrence of acute graft-versus-host disease (HR 2.21; P < .001) and recipient age (HR 1.55; P = .017). Higher lymphocyte AUC at day +30 was significantly associated with low treatment-related mortality (HR, .47; P = .045). Lymphocyte AUC may be a good predictive factor for immune reconstitution against CMV reactivation. It also provides valuable information for predicting HHV-6 reactivation and treatment-related mortality.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier Inc.en
dc.rights© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.rightsThe full-text file will be made open to the public on 1 March 2020 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.rightsThis is not the published version. Please cite only the published version.en
dc.subjectLymphocyte AUCen
dc.subjectHHV-6en
dc.subjectCMV antigenemiaen
dc.subjectViral reactivationen
dc.subjectImmune reconstitutionen
dc.titleLymphocyte Area Under the Curve as a Predictive Factor for Viral Infection after Allogenic Hematopoietic Stem Cell Transplantationen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleBiology of Blood and Marrow Transplantationen
dc.identifier.volume25-
dc.identifier.issue3-
dc.identifier.spage587-
dc.identifier.epage593-
dc.relation.doi10.1016/j.bbmt.2018.10.014-
dc.textversionauthor-
dc.addressDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto Universityen
dc.addressDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto Universityen
dc.identifier.pmid30359733-
dcterms.accessRightsopen access-
datacite.date.available2020-03-01-
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