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脑原在不完全弗氏佐剂中参与诱导哈特利豚鼠实验性变应性脑脊髓炎的作用。

Participation of encephalitogen in incomplete Freund's adjuvant in the induction of experimental allergic encephalomyelitis in Hartley guinea pigs.

作者信息

Lebar R, Vincent C

出版信息

J Neuroimmunol. 1984 Jun;6(3):187-96. doi: 10.1016/0165-5728(84)90005-5.

Abstract

The addition of complete Freund's adjuvant (CFA) to encephalitogen is required for the induction of experimental allergic encephalomyelitis (EAE). On the other hand, administration of encephalitogen in incomplete Freund's adjuvant (IFA) protects the animal from the development of EAE. It is shown in this work that injection of homologous central nervous system (CNS) tissue or myelin basic protein (BP) in IFA, before challenge with CNS tissue in CFA, accelerated the onset of the disease in Hartley guinea pigs. It also appeared to protect the animals, however, because 22% of the group did not develop EAE at all, and in those which did, the disease was not as lethal as in controls. To produce this accelerated form of EAE with encephalitogen in IFA required (1) a time interval shorter than 9 days between the first injection and challenge and (2) that the first injection and the challenge be done in the same site, which could be hind or front foot pads but not the nuchal area. The results indicated that 'priming' by encephalitogen in IFA occurred when this two-step induction procedure was used. The experimental conditions may have bypassed suppressive mechanisms.

摘要

诱导实验性变应性脑脊髓炎(EAE)需要在致脑炎原中添加完全弗氏佐剂(CFA)。另一方面,在不完全弗氏佐剂(IFA)中给予致脑炎原可保护动物不发生EAE。本研究表明,在以CFA中的中枢神经系统(CNS)组织进行攻击之前,在IFA中注射同源CNS组织或髓磷脂碱性蛋白(BP)可加速Hartley豚鼠疾病的发作。然而,这似乎也能保护动物,因为该组中有22%的动物根本没有发生EAE,而在发生EAE的动物中,疾病的致死性不如对照组。要在IFA中用致脑炎原产生这种加速形式的EAE,需要(1)第一次注射与攻击之间的时间间隔短于9天,以及(2)第一次注射和攻击在同一部位进行,该部位可以是后足垫或前足垫,但不是颈部区域。结果表明,当采用这种两步诱导程序时,IFA中的致脑炎原会发生“预激发”。实验条件可能绕过了抑制机制。

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