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实验性自身免疫性脑脊髓炎的起源与应用

The origin and application of experimental autoimmune encephalomyelitis.

作者信息

Baxter Alan G

机构信息

Comparative Genomics Centre, Molecular Sciences Building 21, James Cook University, Townsville, 4,811, Queensland, Australia.

出版信息

Nat Rev Immunol. 2007 Nov;7(11):904-12. doi: 10.1038/nri2190.

Abstract

Experimental autoimmune encephalomyelitis (EAE) is a model of the neuroimmune system responding to priming with central nervous system (CNS)-restricted antigens. It is an excellent model of post-vaccinal encephalitis and a useful model of many aspects of multiple sclerosis. EAE has been established in numerous species and is induced by priming with a large number of CNS-derived antigens. As a consequence, the pathogenesis, pathology and clinical signs vary significantly between experimental protocols. As I describe in this Timeline article, the reductionist approach taken in some lines of investigation of EAE resulted in a reliance on results obtained under a narrow range of conditions. Although such studies made important contributions to our molecular understanding of inflammation, T-cell activation, and MHC restriction, they did not advance as effectively our knowledge of the polyantigenic responses that usually occur in CNS immunopathology and autoimmunity.

摘要

实验性自身免疫性脑脊髓炎(EAE)是神经免疫系统对中枢神经系统(CNS)限制性抗原致敏作出反应的一种模型。它是疫苗接种后脑炎的一个优秀模型,也是多发性硬化症诸多方面的一个有用模型。EAE已在众多物种中建立,并且通过用大量CNS衍生抗原来致敏诱导产生。因此,在不同的实验方案之间,发病机制、病理学和临床体征存在显著差异。正如我在这篇时间轴文章中所描述的,在EAE的某些研究方向上所采用的简化论方法导致了对在狭窄条件范围内获得的结果的依赖。尽管此类研究对我们在分子层面理解炎症、T细胞活化和MHC限制做出了重要贡献,但它们在推进我们对通常发生在CNS免疫病理学和自身免疫中的多抗原反应的了解方面成效不佳。

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