von Hoerschelmann Ellen, Münch Johannes, Gao Linde, Lücht Christian, Naik Marcel G, Schmidt Danilo, Pitzinger Paul, Michel Detlef, Avaniadi Parthenopi, Schrezenmeier Eva, Choi Mira, Halleck Fabian, Budde Klemens
Department of Nephrology and Medical Intensive Care, Charité Universitätsmedizin Berlin, 10117 Berlin, Germany.
Institute of Virology, Charité Universitätsmedizin Berlin, Labor Berlin-Charité-Vivantes GmbH, 10117 Berlin, Germany.
J Clin Med. 2023 Dec 23;13(1):100. doi: 10.3390/jcm13010100.
(1) Background: CMV infections remain a problem after kidney transplantation, particularly if patients are refractory or resistant (r/r) to treatment with valganciclovir (VGCV) or ganciclovir (GCV). (2) Methods: In a single-center retrospective study, kidney transplant recipients (KTR) receiving letermovir (LTV) as rescue therapy for VGCV-/GCV-r/r CMV disease were analyzed regarding CMV history, immunosuppression, and outcomes. (3) Results: Of 201 KTR treated for CMV between 2017 and 2022, 8 patients received LTV following treatment failure with VGCV/GCV. All patients received CMV prophylaxis with VGCV according to the center's protocol, and 7/8 patients had a high-risk (D+/R-) CMV constellation. In seven of eight cases, rising CMV levels occurred during prophylaxis. In seven of eight patients, a mutation in UL97 associated with a decreased response to VGCV/GCV was detected. In four of eight patients, LTV resulted in CMV clearance after 24 ± 10 weeks (16-39 weeks), two of eight patients stabilized at viral loads <2000 cop/mL (6-20 weeks), and two of eight patients developed LTV resistance (range 8-10 weeks). (4) Conclusion: LTV, which is currently evaluated for CMV prophylaxis in kidney transplantation, also shows promising results for the treatment of patients with VGCV/GCV resistance despite the risk of developing LTV resistance. Additional studies are needed to further define its role in the treatment of patients with CMV resistance.
(1)背景:肾移植后巨细胞病毒(CMV)感染仍然是一个问题,特别是当患者对缬更昔洛韦(VGCV)或更昔洛韦(GCV)治疗难治或耐药(r/r)时。(2)方法:在一项单中心回顾性研究中,分析了接受来特莫韦(LTV)作为VGCV/GCV难治性/耐药性CMV疾病挽救治疗的肾移植受者(KTR)的CMV病史、免疫抑制情况和治疗结果。(3)结果:在2017年至2022年期间接受CMV治疗的201例KTR中,8例患者在VGCV/GCV治疗失败后接受了LTV治疗。所有患者均按照中心方案接受VGCV CMV预防,8例患者中有7例具有高危(D+/R-)CMV状态。8例中有7例在预防期间出现CMV水平升高。8例患者中有7例检测到与对VGCV/GCV反应降低相关的UL97突变。8例患者中有4例在24±10周(16 - 39周)后LTV导致CMV清除,8例患者中有2例病毒载量稳定在<2000拷贝/mL(6 - 20周),8例患者中有2例出现LTV耐药(8 - 10周)。(4)结论:目前正在评估用于肾移植CMV预防的LTV,尽管有产生LTV耐药的风险,但在治疗VGCV/GCV耐药患者方面也显示出有前景的结果。需要进一步的研究来进一步确定其在CMV耐药患者治疗中的作用。