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造血干细胞移植患者的巨细胞病毒病:当前及未来的治疗选择

Cytomegalovirus disease in hematopoietic stem cell transplant patients: current and future therapeutic options.

作者信息

Fuji Shigeo, Einsele Hermann, Kapp Markus

机构信息

aDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan bDivision of Hematology/Oncology, Department of Internal Medicine II, University Hospital of Würzburg, Würzburg, Germany.

出版信息

Curr Opin Infect Dis. 2017 Aug;30(4):372-376. doi: 10.1097/QCO.0000000000000375.

Abstract

PURPOSE OF REVIEW

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) has become one of the standard treatment for hematological diseases. Although the clinical outcome has improved significantly during the last decades, the morbidity and mortality after allo-HSCT are still obstacles to cure. Out of major morbidities, opportunistic virus infections such as cytomegalovirus (CMV) infection are important complications, in particular in patients who received human leukocyte antigen-mismatched HSCT. Here, we aim to summarize information about current and future therapeutic options in CMV disease after allo-HSCT.

RECENT FINDINGS

Recently, not only new drugs but also adoptive T-cell therapy are tested in the setting of clinical trials. CMV prophylaxis using letermovir significantly reduced the incidence of CMV disease in comparison to placebo in a phase III clinical trial. Meanwhile, adoptive T-cell therapies which are fully adapted to good manufacturing practice (GMP) conditions are now available. A recent multicenter study in Germany showed a promising result using Streptamer-isolated T-cell therapy.

SUMMARY

With the recent development of CMV-targeted therapy, treatment strategies of CMV infection would be further sophisticated in the near future. VIDEO ABSTRACT: http://links.lww.com/COID/A19.

摘要

综述目的

异基因造血干细胞移植(allo-HSCT)已成为血液系统疾病的标准治疗方法之一。尽管在过去几十年中临床疗效有了显著改善,但allo-HSCT后的发病率和死亡率仍是治愈的障碍。在主要的发病情况中,机会性病毒感染如巨细胞病毒(CMV)感染是重要的并发症,尤其是在接受人类白细胞抗原不匹配的HSCT患者中。在此,我们旨在总结allo-HSCT后CMV疾病当前和未来治疗选择的相关信息。

最新发现

最近,不仅新药,而且过继性T细胞疗法也在临床试验中进行了测试。在一项III期临床试验中,与安慰剂相比,使用来特莫韦进行CMV预防可显著降低CMV疾病的发生率。同时,现在已有完全符合药品生产质量管理规范(GMP)条件的过继性T细胞疗法。德国最近的一项多中心研究显示,使用链霉亲和素分离的T细胞疗法取得了有前景的结果。

总结

随着CMV靶向治疗的最新进展,CMV感染的治疗策略在不久的将来将进一步完善。视频摘要:http://links.lww.com/COID/A19。

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