异基因造血干细胞移植后儿童巨细胞病毒UL97基因耐药相关突变的监测

Q4 Medicine
O.S. ​ Kozhushnaya, G. Solopova, M. I. Markelov, A.R. Oril, D. N. Balashov, L. Shelikhova, G. Novichkova
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引用次数: 0

摘要

目标。对巨细胞病毒(CMV)磷酸转移酶UL97进行基因分型,并研究确诊巨细胞病毒感染的异基因造血干细胞移植(HSCT)后儿童更昔洛韦/缬更昔洛韦(GCV/VGCV)耐药的相关突变。材料与方法。这项单中心前瞻性研究于2020年1月至2021年12月进行,招募了18岁以下确认巨细胞病毒感染的同种异体造血干细胞移植受体。对于可能的GCV抗性,采用Sanger测序进行分子基因分型。结果:在168例确诊的巨细胞病毒感染患者中,72例患者符合GCV/VGCV可能耐药的标准。对19例患者(占患者总数的11.3%,符合耐药标准的患者占26.4%)的CMV UL97基因进行核苷酸测序,鉴定出11种基因型:H520Q、C592G、A594V、L595S、D605E、C603W、C607Y、C607F、M615V、M460V和E655K。12例患者中发现HCV/VHCV耐药相关突变:H520Q、C592G、A594V、L595S、C603W、C607Y、C607F、M460V(占患者总数的7%,符合耐药标准的患者占9.7%)。由于在确认巨细胞病毒感染的同种异体造血移植受体中检测到磷酸转移酶UL97突变形式的频率很高,因此监测耐药相关突变以给予适当的抗病毒治疗非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Monitoring of resistanceassociated mutations in UL97 gene of cytomegalovirus in children after allogeneic hematopoietic stem cell transplantation
Objective. To perform genotyping of cytomegalovirus (CMV) phosphotransferase UL97 and investigate mutations associated with ganciclovir/valganciclovir (GCV/VGCV) resistance in children after allogeneic hematopoietic stem cell transplantation (HSCT) with confirmed CMV infection. Materials and Methods. This single-center prospective study was conducted from January 2020 to December 2021 and enrolled allogeneic HSCT recipients under 18 years of age with confirmed CMV infection. In case of possible GCV resistance, molecular genotyping with Sanger sequencing was performed. The search for mutations in the UL97 gene was carried out in the range of 425–670 codons. Results. Out of 168 patients with confirmed CMV infection, 72 patients met the criteria for possible resistance to GCV/VGCV. As a result of nucleotide sequencing of the CMV UL97 gene in 19 patients (11.3% of a total number of patients and 26.4% of patients meeting the resistance criteria) 11 genotypes of the following mutations were identified: H520Q, C592G, A594V, L595S, D605E, C603W, C607Y, C607F, M615V, M460V and E655K. The following mutations associated with resistance to HCV/VHCV: H520Q, C592G, A594V, L595S, C603W, C607Y, C607F, M460V were found in 12 patients (7% of a total number of patients and 9.7% of patients meeting the resistance criteria). Conclusions. Due to a high frequency of detection of the mutant form of phosphotransferase UL97 in allogeneic HSCT recipients with confirmed CMV infection, it is important to implement monitoring of resistant-associated mutations in order to administer appropriate antiviral therapy.
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CiteScore
0.90
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