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拉替拉韦耐药导致肺移植受者更昔洛韦耐药巨细胞病毒感染

Emergence of letermovir resistance in a lung transplant recipient with ganciclovir-resistant cytomegalovirus infection.

机构信息

Department of Pharmacy Services, Dignity Health, St. Joseph's Hospital and Medical Center, Phoenix, Arizona.

Department of Pharmacy Practice, College of Pharmacy, Midwestern University, Glendale, Arizona.

出版信息

Am J Transplant. 2018 Dec;18(12):3060-3064. doi: 10.1111/ajt.15135. Epub 2018 Oct 29.

Abstract

Following a year of valganciclovir prophylaxis, a lung transplant recipient developed cytomegalovirus (CMV) infection that became resistant to ganciclovir, as confirmed by detection of UL97 kinase mutation M460V and a previously uncharacterized UL54 DNA polymerase mutation L516P. The latter mutation is now shown to confer ganciclovir and cidofovir resistance. As predicted from the viral genotype, foscarnet therapy was effective, but resumption of valganciclovir as secondary prophylaxis resulted in a plasma viral load rebound to 3.6 log copies/mL several weeks later. Valganciclovir was then replaced by letermovir, resulting in gradual viral load reduction in the first 5 weeks to below the quantitation limit (2.7 log copies/mL) for 1 week, followed by 10 weeks of rising viral loads reaching 4.3 log copies/mL while on letermovir. At this point, CMV genotypic testing revealed UL56 mutation C325Y, which confers absolute resistance to letermovir. Retreatment with foscarnet was successful. This case adds to the considerable list of proven ganciclovir resistance mutations, and provides an early experience with letermovir resistance after off-label therapeutic use. This experience is consistent with in vitro observations of rapid emergence of letermovir-resistant CMV after drug exposure.

摘要

在一年的缬更昔洛韦预防治疗后,一名肺移植受者发生了巨细胞病毒(CMV)感染,且对更昔洛韦产生耐药,这通过检测 UL97 激酶突变 M460V 和以前未表征的 UL54 DNA 聚合酶突变 L516P 得到了证实。后者的突变现已证实可导致更昔洛韦和西多福韦耐药。正如病毒基因型所预测的那样,膦甲酸酯治疗有效,但随后恢复使用缬更昔洛韦作为二级预防治疗,数周后导致血浆病毒载量反弹至 3.6 log 拷贝/mL。随后将缬更昔洛韦替换为来特莫韦,在前 5 周内逐渐降低病毒载量,降至定量下限(2.7 log 拷贝/mL)持续 1 周,随后在来特莫韦治疗的 10 周内病毒载量再次升高,达到 4.3 log 拷贝/mL。此时,CMV 基因型检测显示 UL56 突变 C325Y,这导致对来特莫韦绝对耐药。膦甲酸酯重新治疗成功。该病例增加了大量已证实的更昔洛韦耐药突变,为来特莫韦的非标签治疗后出现耐药提供了早期经验。这一经验与药物暴露后迅速出现来特莫韦耐药 CMV 的体外观察结果一致。

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An overview of letermovir: a cytomegalovirus prophylactic option.来特莫韦概述:一种巨细胞病毒预防选择。
Expert Opin Pharmacother. 2019 Aug;20(12):1429-1438. doi: 10.1080/14656566.2019.1637418. Epub 2019 Jul 8.

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