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Gliptin 相关性大疱性类天疱疮具有抗 BP180 和 -BP230 体液反应的独特特征:一项多中心研究的结果。

Gliptin-associated bullous pemphigoid shows peculiar features of anti-BP180 and -BP230 humoral response: Results of a multicenter study.

机构信息

Molecular and Cell Biology Laboratory, IDI-IRCCS, Rome, Italy.

First Dermatology Clinic, IDI-IRCCS, Rome, Italy.

出版信息

J Am Acad Dermatol. 2022 Jul;87(1):56-63. doi: 10.1016/j.jaad.2022.02.036. Epub 2022 Mar 1.

DOI:10.1016/j.jaad.2022.02.036
PMID:35240229
Abstract

BACKGROUND

Recently, several case-control studies demonstrated an association between gliptins and bullous pemphigoid (BP) occurrence. However, data on the clinical and immunologic features of gliptin-associated bullous pemphigoid (GABP) are controversial.

OBJECTIVE

This study aimed to clinically and immunologically characterize a large cohort of GABP patients to get an insight into the pathophysiology of this emerging drug-induced variant of BP.

METHODS

Seventy-four GABP patients were prospectively enrolled and characterized from 9 different Italian dermatology units between 2013 and 2020.

RESULTS

Our findings demonstrated the following in the GABP patients: (1) a noninflammatory phenotype, which is characterized by low amounts of circulating and skin-infiltrating eosinophils, is frequently found; (2) immunoglobulin (Ig)G, IgE, and IgA humoral responses to BP180 and BP230 antigens are reduced in frequency and titers compared with those in patients with idiopathic BP; (3) IgG reactivity targets multiple BP180 epitopes other than noncollagenous region 16A.

LIMITATIONS

A limitation of the study is that the control group did not comprise only type 2 diabetes mellitus patients with BP.

CONCLUSION

GABP patients show peculiar features of anti-BP180 and -BP230 humoral responses, laying the foundation for diagnostic improvements and getting novel insights into understanding the mechanism of BP onset.

摘要

背景

最近,几项病例对照研究表明,二肽基肽酶-4 抑制剂(gliptins)与大疱性类天疱疮(BP)的发生之间存在关联。然而,关于gliptin 相关性大疱性类天疱疮(GABP)的临床和免疫特征的数据仍存在争议。

目的

本研究旨在对大量 GABP 患者进行临床和免疫学特征分析,以深入了解这种新兴的药物诱导的 BP 变异型的发病机制。

方法

2013 年至 2020 年期间,我们从意大利 9 个不同的皮肤科单位前瞻性地纳入并分析了 74 例 GABP 患者。

结果

我们的研究结果表明,GABP 患者具有以下特征:(1)非炎症表型,其特点是循环和皮肤浸润的嗜酸性粒细胞数量较少;(2)与特发性 BP 患者相比,针对 BP180 和 BP230 抗原的免疫球蛋白(Ig)G、IgE 和 IgA 体液反应的频率和滴度降低;(3)IgG 反应靶向 BP180 的多个非胶原区 16A 以外的表位。

局限性

本研究的一个局限性是对照组不仅包括患有 BP 的 2 型糖尿病患者。

结论

GABP 患者表现出针对 BP180 和 BP230 的独特的体液反应特征,为诊断的改进奠定了基础,并为深入了解 BP 发病机制提供了新的见解。

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