Tackling CMV in Transplant Recipients: Past, Present, and Future.

IF 4.7 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2025-06-01 Epub Date: 2025-04-27 DOI:10.1007/s40121-025-01159-6
Tal Schlaeffer-Yosef, Lior Nesher
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引用次数: 0

Abstract

Cytomegalovirus (CMV), a beta-herpesvirus capable of maintaining lifelong latency, presents a substantial risk to transplant recipients, resulting in significant morbidity and mortality among both hematopoietic stem cell and solid organ transplantation recipients. Recent advances have shifted management from reactive approaches, such as preemptive therapy, to preventive strategies to reduce active infections and disease burden. Letermovir, a selective CMV terminase inhibitor, has emerged as a critical prophylactic agent in high-risk transplant populations, significantly lowering infection rates and improving survival with fewer adverse effects than older antivirals. Maribavir, a UL97 kinase inhibitor, is another recently approved promising option for treating CMV, especially in patients with ganciclovir-resistant or refractory CMV infections. Despite these achievements, the risk of late-onset CMV infection after prophylaxis discontinuation remains a significant clinical challenge. Current research seeks to refine prophylactic regimens and develop advanced diagnostic tools, notably interferon-gamma release assays that measure CMV-specific T cell responses. These immunologic assays may help clinicians identify individuals capable of controlling CMV replication, thus guiding the safer discontinuation of prophylaxis and reducing unnecessary drug exposure. Conversely, patients lacking robust immune reconstitution could be targeted for extended prophylaxis or closer follow-up. Looking into the future, ongoing innovations in immune monitoring and antiviral development will likely lead to a more personalized approach to CMV prevention and treatment, optimizing care based on patient-specific risk profiles and immune competence. As this field continues to evolve, integrating novel therapies, improved diagnostics, and immunity-driven protocols holds promise for further reducing CMV-related complications and improving overall outcomes for transplant recipients.

处理移植受者的巨细胞病毒:过去,现在和未来。
巨细胞病毒(CMV)是一种能够维持终身潜伏期的乙型疱疹病毒,对移植受者具有重大风险,在造血干细胞和实体器官移植受者中导致显著的发病率和死亡率。最近的进展已将管理从反应性方法(如先发制人的治疗)转向预防性战略,以减少活动性感染和疾病负担。Letermovir是一种选择性巨细胞病毒终止酶抑制剂,在高危移植人群中已成为一种重要的预防药物,与较老的抗病毒药物相比,它显著降低了感染率,提高了生存率,而且副作用更少。UL97激酶抑制剂Maribavir是最近批准的另一种治疗巨细胞病毒的有希望的选择,特别是对更昔洛韦耐药或难治性巨细胞病毒感染的患者。尽管取得了这些成就,停药后迟发性巨细胞病毒感染的风险仍然是一个重大的临床挑战。目前的研究旨在完善预防方案和开发先进的诊断工具,特别是测量巨细胞病毒特异性T细胞反应的干扰素γ释放测定。这些免疫检测可以帮助临床医生识别有能力控制巨细胞病毒复制的个体,从而指导更安全的停止预防和减少不必要的药物暴露。相反,缺乏强大免疫重建的患者可以针对延长预防或更密切的随访。展望未来,免疫监测和抗病毒药物开发方面的持续创新可能会导致更个性化的巨细胞病毒预防和治疗方法,根据患者特定的风险概况和免疫能力优化护理。随着这一领域的不断发展,整合新疗法、改进诊断和免疫驱动方案有望进一步减少巨细胞病毒相关并发症,改善移植受者的总体预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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