Salvana Edsel Maurice T, Salata Robert A
Division of Infectious Diseases and HIV Medicine, Department of Medicine, University Hospitals Case Medical Center and Case Western Reserve University, Cleveland, Ohio 44106-5083, USA.
Clin Microbiol Rev. 2009 Apr;22(2):274-90, Table of Contents. doi: 10.1128/CMR.00040-08.
Biologics are increasingly becoming part of routine disease management. As more agents are developed, the challenge of keeping track of indications and side effects is growing. While biologics represent a milestone in targeted and specific therapy, they are not without drawbacks, and the judicious use of these "magic bullets" is essential if their full potential is to be realized. Infectious complications in particular are not an uncommon side effect of therapy, whether as a direct consequence of the agent or because of the underlying disease process. With this in mind, we have reviewed and summarized the risks of infection and the infectious disease-related complications for all FDA-approved monoclonal antibodies and some related small molecules, and we discuss the probable mechanisms involved in immunosuppression as well as recommendations for prophylaxis and treatment of specific disease entities.
生物制剂正日益成为常规疾病管理的一部分。随着越来越多的药物被研发出来,跟踪适应症和副作用的挑战也在不断增加。虽然生物制剂代表了靶向和特异性治疗的一个里程碑,但它们并非没有缺点,如果要充分发挥其潜力,明智地使用这些“神奇子弹”至关重要。特别是感染性并发症并非治疗中罕见的副作用,无论是药物的直接后果还是潜在疾病过程导致的。考虑到这一点,我们回顾并总结了所有美国食品药品监督管理局(FDA)批准的单克隆抗体和一些相关小分子的感染风险及与传染病相关的并发症,并讨论了免疫抑制可能涉及的机制以及针对特定疾病实体的预防和治疗建议。