Delayed urticaria during treatment with anti-CGRP monoclonal antibodies in migraine.

IF 4 2区 医学 Q1 CLINICAL NEUROLOGY
Headache Pub Date : 2026-05-01 Epub Date: 2026-03-15 DOI:10.1111/head.70082
Christoph T Berger, Federico Burguet Villena, Severin B Vogt, Lukas Heydrich, Karin Hartmann, Athina Papadopoulou
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引用次数: 0

Abstract

Objective: To characterize clinical presentation and management of urticaria associated with calcitonin gene-related peptide (CGRP) -targeting monoclonal antibodies (mAbs) for migraine prophylaxis.

Background: CGRP-targeting mAbs are effective in migraine prophylaxis, but have been associated with hypersensitivity reactions, including urticaria. The underlying mechanisms, risk factors, and therapeutic consequences of these anti-CGRP mAb-related hypersensitivity reactions remain poorly understood.

Methods: We performed a retrospective case series with descriptive analysis on five patients who developed urticaria after anti-CGRP mAb administration. Timing of reactions, history of urticaria, re-exposure strategies including premedication, and clinical outcomes were analyzed by chart review.

Results: Urticaria occurred after the first injection in three patients and after the third or sixth injection in two. Onset was delayed (12-48 h) in all patients, indicating a non-IgE-mediated hypersensitivity. Four of five patients had a prior history of urticaria. All patients were re-exposed: two to the same anti-CGRP mAb and three to a different. Three patients received H1-antihistamine premedication. All premedicated patients in this series tolerated re-exposure, irrespective of switching. One patient experienced worsening urticaria with repeated dosing without premedication despite negative allergy testing, but later tolerated the same anti-CGRP mAb with premedication. In contrast, urticaria or angioedema recurred in two patients who switched anti-CGRP mAb without premedication. One subsequently tolerated rimegepant.

Conclusion: Anti-CGRP mAb-associated urticaria in this case series was delayed and likely non-immunoglobulin E (non-IgE)-mediated. Our experience supports that in selected patients with delayed urticaria, individualized management, including H1 antihistamine premedication, may allow continuation of effective migraine prophylaxis. Larger cohorts are needed to identify risk factors and to inform general management recommendations.

抗cgrp单克隆抗体治疗偏头痛的延迟性荨麻疹。
目的:探讨降钙素基因相关肽(CGRP)靶向单克隆抗体(mab)预防偏头痛相关荨麻疹的临床表现和治疗。背景:cgrp靶向单克隆抗体在偏头痛预防中有效,但与过敏反应相关,包括荨麻疹。这些抗cgrp单克隆抗体相关的过敏反应的潜在机制、危险因素和治疗后果仍然知之甚少。方法:我们对5例服用抗cgrp单抗后出现荨麻疹的患者进行回顾性病例系列和描述性分析。通过图表回顾分析反应时间、荨麻疹史、再暴露策略(包括用药前)和临床结果。结果:3例患者在第一次注射后出现荨麻疹,2例患者在第三次或第六次注射后出现荨麻疹。所有患者的发病延迟(12-48小时),表明非ige介导的超敏反应。5例患者中有4例既往有荨麻疹病史。所有患者再次暴露:2例使用相同的抗cgrp单抗,3例使用不同的单抗。3例患者接受h1 -抗组胺药预用药。在这个系列中,所有预先用药的患者都能耐受再次暴露,无论是否转换。一名患者在没有预先用药的情况下反复给药,尽管过敏试验呈阴性,但荨麻疹恶化,但后来在预先用药的情况下耐受了相同的抗cgrp单抗。相比之下,在没有预先用药的情况下切换抗cgrp单抗的两名患者中,荨麻疹或血管性水肿复发。一个人随后忍受了巨大的痛苦。结论:本病例系列中抗cgrp单克隆抗体相关性荨麻疹是延迟性的,可能是非免疫球蛋白E(非ige)介导的。我们的经验支持,在选定的延迟性荨麻疹患者中,个体化管理,包括H1抗组胺药物的预用药,可能允许持续有效的偏头痛预防。需要更大的队列来确定风险因素并为一般管理建议提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Headache
Headache 医学-临床神经学
CiteScore
9.40
自引率
10.00%
发文量
172
审稿时长
3-8 weeks
期刊介绍: Headache publishes original articles on all aspects of head and face pain including communications on clinical and basic research, diagnosis and management, epidemiology, genetics, and pathophysiology of primary and secondary headaches, cranial neuralgias, and pains referred to the head and face. Monthly issues feature case reports, short communications, review articles, letters to the editor, and news items regarding AHS plus medicolegal and socioeconomic aspects of head pain. This is the official journal of the American Headache Society.
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