矛盾反应:抗肿瘤坏死因子α药物,Ustekinumab, Secukinumab, Ixekizumab等。

Current problems in dermatology Pub Date : 2018-01-01 Epub Date: 2017-11-07 DOI:10.1159/000479475
Lluís Puig
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引用次数: 89

摘要

在生物制剂治疗期间的矛盾反应可以定义为在治疗患者的另一种通常处于控制之下的疾病时,通常对这类药物有反应的病理状况的出现或恶化(即使可能在形态或表型上发生变化)。矛盾反应最初被描述为使用抗肿瘤坏死因子(TNF) α药物治疗的患者的孤立病例报告或病例系列,首先用于炎症性风湿病,后来用于牛皮癣和炎症性肠病。随后,其他生物药物或类别(如托珠单抗)也报道了矛盾反应,尽管在某些情况下,疗效不足或表型转换可能难以与真正的矛盾反应区分开来。本章将讨论最常见的矛盾反应:掌足底脓疱和银屑病样反应、银屑病关节炎、汗腺炎、炎症性肠病、葡萄膜炎、坏疽性脓皮病、肉芽肿反应和血管炎。在这些涉及多种免疫途径的复杂疾病中,潜在的发病机制很可能是细胞因子失衡,用抗p40或抗il - 17a生物制剂替代抗tnf - α药物可能非常有帮助。矛盾的反应可导致严重的残疾,早期识别和治疗这些药物类效应至关重要,特别是当原发疾病相对缺乏治疗选择,其重新激活可能产生灾难性后果时。密切监测使用新生物药物治疗的患者是必要的,以发现和描述新的矛盾反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paradoxical Reactions: Anti-Tumor Necrosis Factor Alpha Agents, Ustekinumab, Secukinumab, Ixekizumab, and Others.

Paradoxical reactions during treatment with a biologic agent can be defined as the appearance or exacerbation of a pathological condition that usually responds to this class of drug while treating a patient for another condition, which usually remains under control (even though there may be a change in morphology or phenotype). Paradoxical reactions were initially described as isolated case reports or case series in patients treated with anti-tumor necrosis factor (TNF) α agents, first in inflammatory rheumatic diseases, later in psoriasis and inflammatory bowel disease. Paradoxical reactions have subsequently been reported with other biological drugs or classes (e.g., tocilizumab), even though in some cases insufficient efficacy or phenotype switch may be difficult to differentiate from true paradoxical reactions. This chapter will deal with the most frequently reported variants of paradoxical reactions: palmoplantar pustular and psoriasiform reactions, psoriatic arthritis, hidradenitis, inflammatory bowel disease, uveitis, pyoderma gangrenosum, granulomatous reactions, and vasculitis. The underlying pathomechanism in these complex diseases with involvement of multiple immunological pathways is most likely a cytokine imbalance, and substitution of the anti-TNFα agent by an alternative anti-p40 or anti-IL-17A biologic may be extremely helpful. Paradoxical reactions can cause serious handicap, and early recognition and treatment of these drug class effects is of paramount importance, especially when the primary disease is relatively devoid of therapeutic alternatives and its reactivation may have catastrophic consequences. Close surveillance of patients treated with newly available biologic drugs is necessary to detect and describe new paradoxical reactions.

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