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自身抗体在自身免疫性疾病中的作用。

The role of autoantibodies in autoimmune disease.

作者信息

Naparstek Y, Plotz P H

机构信息

Department of Medicine, Hadassah University Hospital, Jerusalem, Israel.

出版信息

Annu Rev Immunol. 1993;11:79-104. doi: 10.1146/annurev.iy.11.040193.000455.

Abstract

In autoimmune diseases, autoantibodies may be the actual pathogenetic agents of the disease, the secondary consequences of tissue damage, or the harmless footprints of an etiologic agent. Establishing a pathogenetic role for autoantibodies requires that they meet stringent criteria. It appears that the location of the presumptive target antigen most critically influences the pathogenetic potential of autoantibodies. Autoantibodies directed against cell surface targets, such as hormone receptors, are clearly pathogenetic; those directed against extracellular targets, such as circulating molecules or extracellular matrix, may or may not cause any damage. Those apparently directed against intracellular targets are usually not pathogenetic unless it can be clearly demonstrated (a) that the antigen is released from within the cell so that it can bind onto a cell surface receptor or other extracellular location, such as proteinase 3; (b) that the antigen moves to an aberrant site on the cell surface, such as, perhaps, the small ribonucleoprotein antigen Ro; or (c) that a cross-reactive molecule, the actual target, such as the membrane ribosomal P-like protein, is at an accessible location.

摘要

在自身免疫性疾病中,自身抗体可能是疾病的实际致病因子、组织损伤的继发后果,或是病因的无害痕迹。确定自身抗体的致病作用需要它们符合严格的标准。看来推测的靶抗原的定位最关键地影响自身抗体的致病潜力。针对细胞表面靶标的自身抗体,如激素受体,显然具有致病性;针对细胞外靶标的自身抗体,如循环分子或细胞外基质,可能会也可能不会造成任何损害。那些明显针对细胞内靶标的自身抗体通常不具有致病性,除非能够明确证明:(a) 抗原从细胞内释放出来,以便它能够结合到细胞表面受体或其他细胞外位置,如蛋白酶3;(b) 抗原移动到细胞表面的异常位点,如小核糖核蛋白抗原Ro;或(c) 一种交叉反应分子,即实际靶标,如膜核糖体P样蛋白,处于可及位置。

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