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ESCMID 研究组(ESGICH)对有合并症宿主感染的共识文件:靶向和生物治疗的安全性:传染病学视角(可溶性免疫效应分子[II]:针对白细胞介素、免疫球蛋白和补体因子的药物)。

ESCMID Study Group for Infections in Compromised Hosts (ESGICH) Consensus Document on the safety of targeted and biological therapies: an infectious diseases perspective (Soluble immune effector molecules [II]: agents targeting interleukins, immunoglobulins and complement factors).

机构信息

Division of Infectious Diseases, Oregon Health and Science University, Portland, OR, USA.

Department of Rheumatology, Hôpitaux Universitaire Paris-Sud, Université Paris-Sud, INSERM U1184, Paris, France.

出版信息

Clin Microbiol Infect. 2018 Jun;24 Suppl 2:S21-S40. doi: 10.1016/j.cmi.2018.02.002. Epub 2018 Feb 12.

Abstract

BACKGROUND

The present review is part of the ESCMID Study Group for Infections in Compromised Hosts (ESGICH) Consensus Document on the safety of targeted and biological therapies.

AIMS

To review, from an Infectious Diseases perspective, the safety profile of agents targeting interleukins, immunoglobulins and complement factors and to suggest preventive recommendations.

SOURCES

Computer-based MEDLINE searches with MeSH terms pertaining to each agent or therapeutic family.

CONTENT

Patients receiving interleukin-1 (IL-1) -targeted (anakinra, canakinumab or rilonacept) or IL-5-targeted (mepolizumab) agents have a moderate risk of infection and no specific prevention strategies are recommended. The use of IL-6/IL-6 receptor-targeted agents (tocilizumab and siltuximab) is associated with a risk increase similar to that observed with anti-tumour necrosis factor-α agents. IL-12/23-targeted agents (ustekinumab) do not seem to pose a meaningful risk of infection, although screening for latent tuberculosis infection may be considered and antiviral prophylaxis should be given to hepatitis B surface antigen-positive patients. Therapy with IL-17-targeted agents (secukinumab, brodalumab and ixekizumab) may result in the development of mild-to-moderate mucocutaneous candidiasis. Pre-treatment screening for Strongyloides stercoralis and other geohelminths should be considered in patients who come from areas where these are endemic who are receiving IgE-targeted agents (omalizumab). C5-targeted agents (eculizumab) are associated with a markedly increased risk of infection due to encapsulated bacteria, particularly Neisseria spp. Meningococcal vaccination and chemoprophylaxis must be administered 2-4 weeks before initiating eculizumab. Patients with high-risk behaviours and their partners should also be screened for gonococcal infection.

IMPLICATIONS

Preventive strategies are particularly encouraged to minimize the occurrence of neisserial infection associated with eculizumab.

摘要

背景

本综述是 ESCMID 感染宿主研究组(ESGICH)靶向和生物治疗安全性共识文件的一部分。

目的

从传染病学的角度回顾靶向白细胞介素、免疫球蛋白和补体因子的药物的安全性概况,并提出预防建议。

来源

使用与每个药物或治疗家族相关的 MeSH 术语进行基于计算机的 MEDLINE 搜索。

内容

接受白细胞介素-1(IL-1)靶向(阿那白滞素、坎那单抗或 rilonacept)或 IL-5 靶向(美泊利珠单抗)药物治疗的患者存在中度感染风险,不推荐特定的预防策略。使用 IL-6/IL-6 受体靶向药物(托珠单抗和西妥昔单抗)与观察到的抗肿瘤坏死因子-α药物相关的风险增加相似。IL-12/23 靶向药物(乌司奴单抗)似乎不会带来有意义的感染风险,尽管可能需要考虑筛查潜伏性结核感染,并且应该给予乙型肝炎表面抗原阳性患者抗病毒预防。使用 IL-17 靶向药物(司库奇尤单抗、布罗达单抗和依奇珠单抗)治疗可能导致轻度至中度黏膜皮肤念珠菌病。来自这些疾病流行地区的患者在接受 IgE 靶向药物(奥马珠单抗)治疗时,应考虑进行肠道蠕虫感染(包括 Strongyloides stercoralis)的筛查。C5 靶向药物(依库珠单抗)与包膜细菌(尤其是奈瑟菌属)感染风险显著增加有关。在开始使用依库珠单抗之前,必须接种脑膜炎球菌疫苗并进行化学预防,时间为 2-4 周。具有高危行为的患者及其伴侣也应筛查淋病感染。

意义

特别鼓励采取预防策略,以最大限度地减少与依库珠单抗相关的奈瑟菌感染的发生。

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