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猫补体C3的分离与鉴定及猫传染性腹膜炎免疫复合物发病机制的证据

Isolation and characterization of feline C3 and evidence for the immune complex pathogenesis of feline infectious peritonitis.

作者信息

Jacobse-Geels H E, Daha M R, Horzinek M C

出版信息

J Immunol. 1980 Oct;125(4):1606-10.

PMID:7410847
Abstract

Infections of cats with feline peritonitis (FIP) virus are usually inapparent but may lead to fatal polyserositis. We have recently advanced the hypothesis that immune complexes play an essential role in the pathogenesis of the condition. To support this hypothesis, the role of the third component of complement in FIP was investigated. In the present paper, the isolation of C3 from normal cat serum and some of its physical and immunologic properties are described. The final protein had an apparent m.w. of 185,000 and was composed of 2 polypeptide chains with m.w. of 128,000 and 71,000, respectively. When tested against whole cat serum, an antiserum raised in rabbits against purified C3 recognized only 1 protein whose identity with C3 was established. With the aid of this antiserum, depositions of C3 in renal glomeruli of FIP-affected cats were demonstrated by immunofluorescence. Their localizaton coincided with that of deposited IgG, thereby supporting the concept of an immune complex pathogenesis of FIP.

摘要

猫感染猫传染性腹膜炎(FIP)病毒通常不表现出明显症状,但可能导致致命的多浆膜炎。我们最近提出了一个假说,即免疫复合物在该病的发病机制中起关键作用。为支持这一假说,我们研究了补体第三成分在FIP中的作用。在本文中,描述了从正常猫血清中分离C3及其一些物理和免疫学特性。最终得到的蛋白质表观分子量为185,000,由两条多肽链组成,分子量分别为128,000和71,000。用兔抗纯化C3血清检测全猫血清时,该血清仅识别一种与C3一致的蛋白质。借助该抗血清,通过免疫荧光法证实了FIP感染猫肾小球中有C3沉积。其定位与沉积的IgG一致,从而支持了FIP免疫复合物发病机制的概念。

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