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脱敏预防药物过敏反应。

Desensitization for the prevention of drug hypersensitivity reactions.

机构信息

Department of Internal Medicine, Gachon University Gil Medical Center, Incheon, Korea.

Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

出版信息

Korean J Intern Med. 2022 Feb;37(2):261-270. doi: 10.3904/kjim.2021.438. Epub 2022 Feb 28.

Abstract

Drug desensitization is the temporary induction of tolerance to a sensitized drug by administering slow increments of the drug, starting from a very small amount to a full therapeutic dose. It can be used as a therapeutic strategy for patients with drug hypersensitivity when no comparable alternatives are available. Desensitization has been recommended for immunoglobulin E (IgE)-mediated immediate hypersensitivity; however, its indications have recently been expanded to include non-IgE-mediated, non-immunological, or delayed T cell-mediated reactions. Currently, the mechanism of desensitization is not fully understood. However, the attenuation of various intracellular signals in target cells is an area of active research, such as high-affinity IgE receptor (FcεRI) internalization, anti-drug IgG4 blocking antibody, altered signaling pathways in mast cells and basophils, and reduced Ca2+ influx. Agents commonly requiring desensitization include antineoplastic agents, antibiotics, antituberculous agents, and aspirin/nonsteroidal antiinflammatory drugs. Various desensitization protocols (rapid or slow, multi-bag or one-bag, with different target doses) have been proposed for each drug. An appropriate protocol should be selected with the appropriate concentration, dosage, dosing interval, and route of administration. In addition, the protocol should be adjusted with consideration of the severity of the initial reaction, the characteristics of the drug itself, as well as the frequency, pattern, and degree of breakthrough reactions.

摘要

药物脱敏是通过缓慢递增药物剂量,从非常小的量开始逐渐增加到全治疗剂量,来暂时诱导对致敏药物的耐受性。当没有可比较的替代药物时,它可以作为药物过敏患者的治疗策略。脱敏已被推荐用于免疫球蛋白 E(IgE)介导的即刻过敏反应;然而,其适应证最近已扩展到包括非 IgE 介导、非免疫或迟发性 T 细胞介导的反应。目前,脱敏的确切机制尚不完全清楚。然而,目标细胞中各种细胞内信号的衰减是一个活跃的研究领域,例如高亲和力 IgE 受体(FcεRI)内化、抗药物 IgG4 阻断抗体、肥大细胞和嗜碱性粒细胞中信号通路的改变以及 Ca2+内流的减少。通常需要脱敏的药物包括抗肿瘤药物、抗生素、抗结核药物和阿司匹林/非甾体抗炎药。针对每种药物,已经提出了各种脱敏方案(快速或缓慢、多袋或单袋、不同的目标剂量)。应根据初始反应的严重程度、药物本身的特性以及突破性反应的频率、模式和程度选择适当的方案。此外,应考虑调整方案,以适应初始反应的严重程度、药物本身的特性以及突破性反应的频率、模式和程度。

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