Kelsey Andrew, Chirch Lisa M, Payette Michael J
University of Connecticut Health Center, Farmington, CT.
Dermatol Online J. 2018 Sep 15;24(9):13030/qt58j4n38m.
Several new monoclonal antibodies that interfere with interleukin (IL) cascades have come to market in recent years. They follow a generation of drugs that block tumor necrosis factor (TNF). It has been well established that TNF is important in the containment of Mycobacterium tuberculosis (Mtb) and that blocking this cytokine increases the risk of tuberculosis (TB) infection. Thus, judicious screening for Mtb of patients taking TNF blocking drugs has been the standard of care. It remains unclear if the newer monoclonal, interleukin blocking drugs, which affect IL-12, IL-23, and IL-17 pathways are associated with risk of Mtb reactivation. Herein we discuss what is known about the immunologic response to Mtb and discuss the data that is currently available for the new interleukin monoclonal antibody blocking medications regarding the risk of latent TB reactivation or active TB infection.
近年来,几种干扰白细胞介素(IL)级联反应的新型单克隆抗体已上市。它们是继一代阻断肿瘤坏死因子(TNF)的药物之后出现的。TNF在遏制结核分枝杆菌(Mtb)方面的重要性已得到充分证实,阻断这种细胞因子会增加结核病(TB)感染的风险。因此,对服用TNF阻断药物的患者进行Mtb的审慎筛查一直是标准治疗方法。目前尚不清楚影响IL-12、IL-23和IL-17途径的新型白细胞介素阻断单克隆药物是否与Mtb再激活风险相关。在此,我们讨论已知的对Mtb的免疫反应,并讨论目前可获得的关于新型白细胞介素单克隆抗体阻断药物潜伏性TB再激活或活动性TB感染风险的数据。