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dc.contributor.author문영철*
dc.date.accessioned2016-08-27T04:08:35Z-
dc.date.available2016-08-27T04:08:35Z-
dc.date.issued2015*
dc.identifier.issn1386-6532*
dc.identifier.issn1873-5967*
dc.identifier.otherOAK-16062*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/217854-
dc.description.abstractBackground: The incidence of herpes zoster is substantial during bortezomib treatment in patients with multiple myeloma (MM). Objectives: This study aimed to elucidate the effect of chemotherapy with or without bortezomib in MM patients on their herpes zoster incidence and varicella zoster virus (VZV)-specific cell-mediated immunity (CMI). Study design: Peripheral blood mononuclear cells were collected at baseline and after 1 month of bortezomib-based or thalidomide-based chemotherapy and then analyzed using VZV-specific interferongamma (IFN-gamma) enzyme-linked immunospot (ELISPOT) assay. The clinical data from these patients were analyzed in relation to the ELISPOT results. Results: Of 58 patients analyzed, 39 patients received bortezomib and the other 19 patients, thalidomide. Among them, 5 patients developed herpes zoster during chemotherapy; all 5 were being treated with the bortezomib-based regimen and were not receiving prophylactic anti-viral agents. The median onset of herpes zoster was 32 days (range, 15-95 days) from the initiation of chemotherapy. Among patients who received bortezomib therapy, acyclovir prophylaxis significantly reduced the risk for herpes zoster (100-day cumulative incidence, 0% vs. 49.5%; p < 0.001). Spot-forming cell (SFC) counts in the IFN-gamma ELISPOT assay decreased from baseline after bortezomib (p = 0.011) or thalidomide (p = 0.096) treatment. Patients with baseline SFCs greater than 20/10(6) mononuclear cells exhibited significantly higher incidence of herpes zoster (100-day cumulative incidence, 34.8% vs. 0%; p = 0.040). Conclusions: Bortezomib treatment significantly reduced VZV-specific CMI, and high baseline SFC counts in patients receiving this treatment without acyclovir prophylaxis were associated with a significantly increased risk for herpes zoster. (C) 2015 Elsevier B.V. All rights reserved.*
dc.languageEnglish*
dc.publisherELSEVIER SCIENCE BV*
dc.subjectVaricella-zoster virus*
dc.subjectEnzyme-linked immunospot assay*
dc.subjectHerpes zoster*
dc.subjectMultiple myeloma*
dc.subjectBortezomib*
dc.titleVaricella-zoster virus-specific cell-mediated immunity and herpes zoster development in multiple myeloma patients receiving bortezomib- or thalidomide-based chemotherapy*
dc.typeArticle*
dc.relation.volume73*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage64*
dc.relation.lastpage69*
dc.relation.journaltitleJOURNAL OF CLINICAL VIROLOGY*
dc.identifier.doi10.1016/j.jcv.2015.10.018*
dc.identifier.wosidWOS:000367390700013*
dc.identifier.scopusid2-s2.0-84949449433*
dc.author.googleKim, Ji-Won*
dc.author.googleMin, Chang-Ki*
dc.author.googleMun, Yeung-Chul*
dc.author.googlePark, Yong*
dc.author.googleKim, Byung Soo*
dc.author.googleNam, Seung-Hyun*
dc.author.googleKoh, Youngil*
dc.author.googleKwon, Ji-Hyun*
dc.author.googleChoe, Pyoeng Gyun*
dc.author.googlePark, Wan Beom*
dc.author.googleKim, Inho*
dc.contributor.scopusid문영철(7003363716)*
dc.date.modifydate20240422115947*
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의과대학 > 의학과 > Journal papers
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