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内皮,结缔组织病中免疫介导攻击的靶点。

Endothelium, a target for immune-mediated assault in connective tissue disease.

作者信息

Youinou Pierre, Le Dantec Christelle, Bendaoud Boutahar, Renaudineau Yves, Pers Jacques-Olivier, Jamin Christophe

机构信息

Laboratory of Immunology Brest University Medical School Hospital BP824, F29609, Brest Cedex, France.

出版信息

Autoimmun Rev. 2006 Mar;5(3):222-8. doi: 10.1016/j.autrev.2005.06.012. Epub 2005 Aug 19.

Abstract

Evidence is lacking that antibodies (Ab) to endothelial cells (AECA) are pathogenic. They are frequently associated with antiphospholipid Ab (aPL), binding to complexes of phosphatidylserine (PS) with beta2GPI. Recent studies have, however, kindled a new debate on their pathogenicity of AECA. A group is responsible for PS reaching the surface of a cell, a feature of commitment to apoptosis. Defective clearance by macrophages of AECA-induced apoptotic cells might display beta2GPI on their surface, and challenge T cell tolerance, until aPL production. Some AECA are thus induced by cell membrane structures, while others recognize "planted" antigens and possibly ligand-receptor complexes. A second group promotes procoagulant factor, and a third has the capacity to trigger apoptosis. Clearly, the most direct demonstration of the pathogenicity of AECA is the autoAb-induced murine model of vasculiltis.

摘要

缺乏证据表明抗内皮细胞抗体(AECA)具有致病性。它们常与抗磷脂抗体(aPL)相关,可与磷脂酰丝氨酸(PS)与β2糖蛋白I的复合物结合。然而,最近的研究引发了关于AECA致病性的新争论。一组负责PS到达细胞表面,这是细胞凋亡的一个特征。巨噬细胞对AECA诱导的凋亡细胞清除缺陷可能会使其表面呈现β2糖蛋白I,并挑战T细胞耐受性,直至产生aPL。因此,一些AECA是由细胞膜结构诱导的,而另一些则识别“植入”的抗原以及可能的配体-受体复合物。第二组促进促凝因子,第三组有触发凋亡的能力。显然,AECA致病性最直接的证明是自身抗体诱导的血管炎小鼠模型。

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