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疱疹样皮炎的病因发病机制。

Etiopathogenesis of dermatitis herpetiformis.

作者信息

Rybak-d'Obyrn Joanna, Placek Waldemar

机构信息

Department of Dermatology, Sexually Transmitted Diseases and Clinical Immunology, University of Warmia and Mazury, Olsztyn, Poland.

出版信息

Postepy Dermatol Alergol. 2022 Feb;39(1):1-6. doi: 10.5114/ada.2020.101637. Epub 2022 Feb 28.

Abstract

Dermatitis herpetiformis is a rare chronic, autoimmune bullous disease linked to gluten sensitivity with intense pruritus and characteristic skin eruptions. Etiopathogenesis is complex and not fully understood. It is currently considered to be a specific cutaneous manifestation of celiac disease. Genetic, environmental and immunological factors influence both conditions. Exposure to gluten is the starting point of an inflammatory cascade leading to the formation of circulating IgA antibodies against tissue transglutaminase and skin immune IgA deposition followed by skin lesions. Binding of the immune complex deposits of IgA transglutaminases and epidermal antibodies with enzymes in the papillary dermis stimulates complement activation, neutrophil influx, proinflammatory cytokine release and overproduction of matrix metalloproteinases. We have collected current knowledge of the pathogenesis of dermatitis herpetiformis.

摘要

疱疹样皮炎是一种罕见的慢性自身免疫性大疱性疾病,与麸质敏感性相关,伴有剧烈瘙痒和特征性皮肤疹。病因发病机制复杂,尚未完全了解。目前认为它是乳糜泻的一种特异性皮肤表现。遗传、环境和免疫因素影响这两种疾病。接触麸质是炎症级联反应的起点,导致循环中针对组织转谷氨酰胺酶的IgA抗体形成和皮肤免疫IgA沉积,随后出现皮肤病变。IgA转谷氨酰胺酶和表皮抗体的免疫复合物沉积物与乳头真皮中的酶结合,刺激补体激活、中性粒细胞流入、促炎细胞因子释放和基质金属蛋白酶的过度产生。我们收集了目前关于疱疹样皮炎发病机制的知识。

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