Department of Infectious Diseases, Infection Control, and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Curr Opin Infect Dis. 2019 Dec;32(6):565-574. doi: 10.1097/QCO.0000000000000607.
Refractory or resistant cytomegalovirus (CMV) infections are challenging complications after hematopoietic cell transplantation (HCT). Most refractory or resistant CMV infections are associated with poor outcomes and increased mortality. Prompt recognition of resistant or refractory CMV infections, understanding the resistance pathways, and the treatment options in HCT recipients are imperative.
New definitions for refractory and resistant CMV infections in HCT recipients have been introduced for future clinical trials. Interestingly, refractory CMV infections are more commonly encountered in HCT recipients when compared with resistant CMV infections. CMV terminase complex mutations in UL56, UL89, and UL51 could be associated with letermovir resistance; specific mutations in UL56 are the most commonly encountered in clinical practice. Finally, brincidofovir, maribavir, letermovir, and CMV-specific cytotoxic T-cell therapy expanded our treatment options for refractory or resistant CMV infections.
Many advances have been made to optimize future clinical trials for management of refractory or resistant CMV infections, and to better understand new resistance mechanisms to novel drugs. New drugs or strategies with limited toxicities are needed to improve outcomes of difficult to treat CMV infections in HCT recipients.
造血细胞移植(HCT)后出现难治性或耐药性巨细胞病毒(CMV)感染是一种棘手的并发症。大多数难治性或耐药性 CMV 感染与不良结局和死亡率增加有关。因此,及时识别难治性或耐药性 CMV 感染、了解耐药途径以及 HCT 受者的治疗选择至关重要。
为未来的临床试验引入了 HCT 受者中难治性和耐药性 CMV 感染的新定义。有趣的是,与耐药性 CMV 感染相比,HCT 受者中更常出现难治性 CMV 感染。UL56、UL89 和 UL51 中的 CMV 末端酶复合物突变可能与来特莫韦耐药相关;在临床实践中,最常遇到 UL56 中的特定突变。最后,布西利福韦、马拉韦罗、来特莫韦和 CMV 特异性细胞毒性 T 细胞治疗扩大了我们对难治性或耐药性 CMV 感染的治疗选择。
为优化难治性或耐药性 CMV 感染管理的未来临床试验,并更好地了解新型药物的新耐药机制,已经取得了许多进展。需要具有有限毒性的新药或策略来改善 HCT 受者中难以治疗的 CMV 感染的结局。