Department of Laboratory Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Catholic Genetic Laboratory Center, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Viruses. 2023 May 30;15(6):1286. doi: 10.3390/v15061286.
Cytomegalovirus (CMV) infection is a serious complication in hematopoietic cell transplantation (HCT) recipients. Drug-resistant strains make it more challenging to treat CMV infection. This study aimed to identify variants associated with CMV drug resistance in HCT recipients and assess their clinical significance. A total of 123 patients with refractory CMV DNAemia out of 2271 HCT patients at the Catholic Hematology Hospital between April 2016 and November 2021 were analyzed, which accounted for 8.6% of the 1428 patients who received pre-emptive therapy. Real-time PCR was used to monitor CMV infection. Direct sequencing was performed to identify drug-resistant variants in and . Resistance variants were found in 10 (8.1%) patients, and variants of uncertain significance (VUS) were found in 48 (39.0%) patients. Patients with resistance variants had a significantly higher peak CMV viral load than those without ( = 0.015). Patients with any variants had a higher risk of severe graft-versus-host disease and lower one-year survival rates than those without ( = 0.003 and = 0.044, respectively). Interestingly, the presence of variants reduced the rate of CMV clearance, particularly in patients who did not modify their initial antiviral regimen. However, it had no apparent impact on individuals whose antiviral regimens were changed due to refractoriness. This study highlights the importance of identifying genetic variants associated with CMV drug resistance in HCT recipients for providing appropriate antiviral treatment and predicting patient outcomes.
巨细胞病毒(CMV)感染是造血细胞移植(HCT)受者的严重并发症。耐药株使得治疗 CMV 感染更加具有挑战性。本研究旨在鉴定与 HCT 受者 CMV 耐药相关的变异体,并评估其临床意义。对 2016 年 4 月至 2021 年 11 月期间天主教血液病医院 2271 例 HCT 患者中出现难治性 CMV DNA 血症的 123 例患者(占接受预防性治疗的 1428 例患者的 8.6%)进行了分析。实时 PCR 用于监测 CMV 感染。直接测序用于鉴定 和 中的耐药变异体。在 10 例(8.1%)患者中发现耐药变异体,在 48 例(39.0%)患者中发现意义不明的变异体(VUS)。携带耐药变异体的患者的 CMV 病毒载量峰值明显高于未携带的患者( = 0.015)。携带任何变异体的患者发生严重移植物抗宿主病的风险和 1 年生存率均高于未携带的患者( = 0.003 和 = 0.044)。有趣的是,变异体的存在降低了 CMV 清除率,尤其是在未改变初始抗病毒方案的患者中。然而,对于因耐药性而改变抗病毒方案的个体,这种变异体似乎没有明显影响。本研究强调了鉴定与 HCT 受者 CMV 耐药相关的遗传变异体的重要性,以便为患者提供适当的抗病毒治疗并预测患者结局。