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T细胞肽中分子模拟的频率作为自身免疫性疾病和自身抗体诱导的基础。

Frequency of molecular mimicry among T cell peptides as the basis for autoimmune disease and autoantibody induction.

作者信息

Garza K M, Tung K S

机构信息

Department of Microbiology, University of Virginia, Charlottesville 22908, USA.

出版信息

J Immunol. 1995 Dec 1;155(11):5444-8.

PMID:7594562
Abstract

Experimental ovarian autoimmune disease is inducible by immunization with an ovarian peptide from zona pellucida (ZP) 3, a glycoprotein of the zona pellucida on mouse oocyte. The murine ZP3 peptide contains two nested T cell epitopes with slightly different critical residue motifs. To investigate the frequency of cross-reaction between nonovarian and ovarian peptides, we have chosen arbitrarily 16 nonovarian peptides with complete or partial homology to the critical residue motifs of the two T cell epitopes. Based on peptide induction of autoimmune oophoritis and T cell-dependent amplified autoantibody response to ovarian ZP, cross-reaction was documented for 7 (or 44%) of the 16 nonovarian peptides studied. Thus, molecular mimicry as a pathogenetic mechanism of autoimmunity should not be limited by the frequency of cross-reaction among self and nonself peptides. On the other hand, the sharing of critical residue motif per se is not sufficient for mimicry to occur, nor does it predict peptide cross-reaction.

摘要

实验性卵巢自身免疫性疾病可通过用来自透明带(ZP)3的卵巢肽进行免疫诱导,ZP3是小鼠卵母细胞透明带上的一种糖蛋白。小鼠ZP3肽包含两个嵌套的T细胞表位,其关键残基基序略有不同。为了研究非卵巢肽与卵巢肽之间的交叉反应频率,我们任意选择了16种与两个T细胞表位的关键残基基序具有完全或部分同源性的非卵巢肽。基于肽诱导的自身免疫性卵巢炎以及对卵巢ZP的T细胞依赖性自身抗体反应增强,在所研究的16种非卵巢肽中,有7种(或44%)出现了交叉反应。因此,分子模拟作为自身免疫的一种致病机制不应受自身肽与非自身肽之间交叉反应频率的限制。另一方面,关键残基基序本身的共享不足以发生模拟,也不能预测肽的交叉反应。

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