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蛋白酶抑制剂α-2-巨球蛋白样-1 是人类副肿瘤天疱疮自身抗体识别的 p170 抗原。

The protease inhibitor alpha-2-macroglobulin-like-1 is the p170 antigen recognized by paraneoplastic pemphigus autoantibodies in human.

机构信息

Department of Dermatology, Inselspital, Bern University Hospital and University of Bern, Bern, Switzerland.

出版信息

PLoS One. 2010 Aug 18;5(8):e12250. doi: 10.1371/journal.pone.0012250.

Abstract

BACKGROUND

Paraneoplastic pemphigus (PNP) is a devastating autoimmune blistering disease, involving mucocutaneous and internal organs, and associated with underlying neoplasms. PNP is characterized by the production of autoantibodies targeting proteins of the plakin and cadherin families involved in maintenance of cell architecture and tissue cohesion. Nevertheless, the identity of an antigen of Mr 170,000 (p170), thought to be critical in PNP pathogenesis, has remained unknown.

METHODOLOGY/PRINCIPAL FINDINGS: Using an immunoprecipitation and mass spectrometry based approach, we identified p170 as alpha-2-macroglobuline-like-1, a broad range protease inhibitor expressed in stratified epithelia and other tissues damaged in the PNP disease course. We demonstrate that 10 PNP sera recognize alpha-2-macroglobuline-like-1 (A2ML1), while none of the control sera obtained from patients with bullous pemphigoid, pemphigus vulgaris, pemphigus foliaceus and normal subjects does.

CONCLUSIONS/SIGNIFICANCE: Our study unravels a broad range protease inhibitor as a new class of target antigens in a paraneoplastic autoimmune multiorgan syndrome and opens a new challenging investigation avenue for a better understanding of PNP pathogenesis.

摘要

背景

副肿瘤天疱疮(PNP)是一种严重的自身免疫性水疱病,涉及黏膜和内脏器官,并与潜在的肿瘤有关。PNP 的特征是产生针对桥粒和钙黏蛋白家族蛋白的自身抗体,这些蛋白参与维持细胞结构和组织内聚。然而,被认为在 PNP 发病机制中起关键作用的 Mr 170,000(p170)抗原的身份仍然未知。

方法/主要发现:我们使用免疫沉淀和基于质谱的方法,将 p170 鉴定为α-2-巨球蛋白样-1(A2ML1),这是一种广谱蛋白酶抑制剂,在表皮分层和 PNP 疾病过程中受损的其他组织中表达。我们证明 10 种 PNP 血清识别α-2-巨球蛋白样-1(A2ML1),而从大疱性类天疱疮、寻常型天疱疮、落叶型天疱疮和正常受试者获得的对照血清中没有一种识别。

结论/意义:我们的研究揭示了广谱蛋白酶抑制剂作为一种新的靶抗原类,存在于副肿瘤性自身免疫多器官综合征中,并为更好地理解 PNP 发病机制开辟了新的具有挑战性的研究途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aea/2923615/df7f2bdd6ed2/pone.0012250.g001.jpg

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