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生物标志物、自身抗原与免疫缩影。

Biomarkers, self-antigens and the immunological homunculus.

作者信息

Cohen Irun R

机构信息

Department of Immunology, The Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

J Autoimmun. 2007 Dec;29(4):246-9. doi: 10.1016/j.jaut.2007.07.016. Epub 2007 Sep 20.

Abstract

The notion of the immunological homunculus arose from the observations (1) that the healthy adaptive immune system is inclined to respond (T cell reactivity and autoantibodies) to particular sets of body molecules (self-antigens) and (2) that autoimmune diseases are characterized by sets of autoimmune reactivity to some of the very same self-antigens recognized by healthy subjects - with an obvious difference in outcome. I termed this natural autoimmune structuring of the immune system, the immunological homunculus - the immune system's representation of the body. What might be the selective advantage of an immune system expressing patterns of built-in autoimmunity to particular sets of self-molecules? To better characterize the homunculus, we have used informatic tools to study patterns of antibodies to many hundreds of self-molecules arrayed on glass slides - an antigen chip of our design. Results using the antigen chip suggest that the particular self-reactivities comprising the homunculus could serve as a set of biomarkers that help the immune system initiate and regulate the inflammatory processes that maintain the body.

摘要

免疫小人的概念源于以下观察结果

(1)健康的适应性免疫系统倾向于对特定的身体分子(自身抗原)产生反应(T细胞反应性和自身抗体);(2)自身免疫性疾病的特征是对健康个体识别的某些相同自身抗原产生一系列自身免疫反应——只是结果明显不同。我将免疫系统的这种自然自身免疫结构称为免疫小人——免疫系统对身体的表征。表达针对特定自身分子的内置自身免疫模式的免疫系统有什么选择优势呢?为了更好地描述免疫小人,我们使用信息工具研究了排列在玻片上的数百种自身分子的抗体模式——这是我们设计的一种抗原芯片。使用抗原芯片的结果表明,构成免疫小人的特定自身反应性可以作为一组生物标志物,帮助免疫系统启动和调节维持身体的炎症过程。

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