How I prevent viral reactivation in high-risk patients

被引:21
作者
Dadwal, Sanjeet S. [1 ]
Papanicolaou, Genovefa A. [2 ,3 ]
Boeckh, Michael [4 ,5 ,6 ]
机构
[1] City Hope Natl Med Ctr, Dept Med, Div Infect Dis, Duarte, CA USA
[2] Mem Sloan Kettering Canc Ctr, Infect Dis Serv, New York, NY USA
[3] Cornell Univ, Weill Cornell Med Coll, Dept Med, New York, NY USA
[4] Fred Hutchinson Canc Ctr, Vaccine & Infect & Clin Res Div, Seattle, WA USA
[5] Univ Washington, Dept Med, Div Allergy & Infect Dis, Seattle, WA USA
[6] Fred Hutchinson Canc Ctr, 1100 Fairview Ave N, Seattle, WA 98109 USA
基金
美国国家卫生研究院;
关键词
STEM-CELL TRANSPLANTATION; VERSUS-HOST-DISEASE; VARICELLA-ZOSTER-VIRUS; CYTOMEGALOVIRUS-INFECTION; ADENOVIRUS INFECTION; T-CELLS; HEMORRHAGIC CYSTITIS; PREEMPTIVE THERAPY; DOUBLE-BLIND; IMMUNE RECONSTITUTION;
D O I
10.1182/blood.2021014676
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Preventing viral infections at an early stage is a key strategy for successfully improving transplant outcomes. Pre-emptive therapy and prophylaxis with antiviral agents have been successfully used to prevent clinically significant viral infections in hematopoietic cell transplant recipients. Major progress has been made over the past decades in preventing viral infections through a better understanding of the biology and risk factors, as well as the introduction of novel antiviral agents and advances in immunotherapy. High-quality evidence exists for the effective prevention of herpes simplex virus, varicella-zoster virus, and cytomegalovirus infection and disease. Few data are available on the effective prevention of human herpesvirus 6, Epstein-Barr virus, adenovirus, and BK virus infections. To highlight the spectrum of clinical practice, here we review high-risk situations that we handle with a high degree of uniformity and cases that feature differences in approaches, reflecting distinct hematopoietic cell transplant practices, such as ex vivo T-cell depletion.
引用
收藏
页码:2062 / 2074
页数:13
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