Microbiology Department, Hospital Clinic I Provincial de Barcelona, Institut of Global Health of Barcelona (ISGlobal), Barcelona, Spain.
National Reference Center for Cytomegaloviruses, Microbiology Department, Centre Hospitalier Universitaire Limoges, Institut national de la santé et de la recherche médicale 1092, Limoges, France.
J Infect Dis. 2021 Sep 17;224(6):1024-1028. doi: 10.1093/infdis/jiab029.
Two transplant recipients (1 kidney and 1 hematopoietic stem cell) received maribavir (MBV) after cytomegalovirus (CMV) infection clinically resistant to standard therapy. Both patients achieved CMV DNA clearance within 30 and 18 days; however, the UL97 C480F variant emerged, causing recurrent CMV infection after a cumulative 2 months of MBV and 15 or 4 weeks of ganciclovir treatment, respectively. C480F was not detected under ganciclovir before MBV treatment. Recombinant phenotyping showed that C480F conferred the highest level of MBV resistance and ganciclovir cross-resistance, with impaired viral growth. Clinical follow-up and genotypic and phenotypic studies are essential for the assessment and optimization of patients with suspected MBV resistance.
两名移植受者(1 例肾移植和 1 例造血干细胞移植)在临床证实对标准治疗药物产生抗药性的巨细胞病毒(CMV)感染后接受了马拉韦罗(MBV)治疗。两名患者均在 30 天和 18 天内清除了 CMV DNA;然而,UL97 C480F 变异体出现,分别导致在接受 MBV 治疗累积 2 个月和更久的 15 周或 4 周的更昔洛韦治疗后出现复发性 CMV 感染。在接受 MBV 治疗之前,更昔洛韦治疗下未检测到 C480F。重组表型分析表明,C480F 导致 MBV 耐药性和更昔洛韦交叉耐药性最高,病毒生长受损。临床随访以及基因和表型研究对于评估和优化疑似 MBV 耐药性患者至关重要。