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The impact of drug-resistant cytomegalovirus in pediatric allogeneic hematopoietic cell transplant recipients: a prospective monitoring of UL97 and UL54 gene mutations

Authors
Choi, S. -H.Hwang, J. -Y.Park, K. -S.Kim, Y.Lee, S. H.Yoo, K. H.Kang, E. -S.Ahn, J. -H.Sung, K. W.Koo, H. H.Kim, Y. -J.
Issue Date
12월-2014
Publisher
WILEY
Keywords
cytomegalovirus; drug resistance; ganciclovir kinase; UL54 protein; hematopoietic stem cell transplantation
Citation
TRANSPLANT INFECTIOUS DISEASE, v.16, no.6, pp.919 - 929
Indexed
SCIE
SCOPUS
Journal Title
TRANSPLANT INFECTIOUS DISEASE
Volume
16
Number
6
Start Page
919
End Page
929
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/96584
DOI
10.1111/tid.12311
ISSN
1398-2273
Abstract
BackgroundCytomegalovirus (CMV) infection is a major cause of morbidity in allogeneic hematopoietic cell transplant (alloHCT) recipients. Little is known about the epidemiology of antiviral resistance in the pediatric population. We performed the prospective study to assess the impact of drug-resistant CMV infections in pediatric alloHCT recipients. MethodsPediatric alloHCT recipients who developed CMV infection were consecutively enrolled from May 2009 to April 2012. CMV polymerase chain reaction amplification and sequencing analysis for UL97 and UL54 genes were performed at enrollment and during follow-up. ResultsIn total, 208 sequence data from viruses in 49 recipients were eligible for the final analysis. Resistant CMV infection caused by UL97 and UL54 mutations occurred in 4.1% (2/49) and 2.0% (1/49), respectively. Known UL97 mutations, M460V and C592G, were observed in each of 2 patients. One patient with the M460V UL97 mutation had an additional T700A UL54 mutation. Drug-resistant CMV attributable mortality was 2.0% (1/49). One or more known sequence variants (drug-sensitive) were observed in all 49 patients. Thirty-one (63.3%) and 28 patients (60.9%) already had known UL97 and UL54 sequence variants before antiviral therapy, respectively. ConclusionThis study provides comprehensive information on the epidemiology of both UL97 and UL54 variants and mutations in alloHCT recipients.
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