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识别嗜神经性弗氏小鼠白血病病毒的单克隆抗体的特性分析

Characterization of monoclonal antibodies recognizing neurotropic Friend murine leukemia virus.

作者信息

Ikeda T, Takase-Yoden S, Watanabe R

机构信息

Institute of Life Science, Soka University, Tokyo, Japan.

出版信息

Virus Res. 1995 Oct;38(2-3):297-304. doi: 10.1016/0168-1702(95)00066-y.

Abstract

We isolated a replication-competent, neurotropic retrovirus (FrC6 virus) and its molecular clone A8 from the NB-tropic Friend murine leukemia virus (FLV) complex. For detection and characterization of the FrC6 and A8 viruses, monoclonal antibodies (MAbs) against the FLV complex were established. Thirty MAbs, each of which reacted with the FLV-producing cell line, were tested for potential neutralizing activities; only two MAbs inhibited the proliferation of the A8 virus. These two MAbs were ineffective or had very weak neutralizing activities toward the non-neurotropic FLV strain clone 57 virus. Further characterization of MAbs by immunoprecipitation revealed that 4 MAbs recognized the envelope protein of the A8 virus. Two of these 4 MAbs recognized the surface glycoprotein gp70, requiring the conformational epitope of the virus for this recognition, while the other two MAbs, which were reactive with the transmembrane protein p15E, were conformation-independent. Both of the MAbs against gp70 distinguished neuropathogenic and non-neuropathogenic viruses to some extent, through neutralizing activity or binding activity detected by immunoprecipitation, whereas the two MAbs against p15E reacted with the viruses in a similar manner. Furthermore, one of the MAbs distinguished the viral antigen in the wall of the vacuolation that composes the spongiotic lesion induced by FrC6 viral infection of the brain.

摘要

我们从嗜NB的弗氏小鼠白血病病毒(FLV)复合体中分离出一种具有复制能力的嗜神经逆转录病毒(FrC6病毒)及其分子克隆A8。为了检测和鉴定FrC6和A8病毒,制备了针对FLV复合体的单克隆抗体(MAb)。对30种与产生FLV的细胞系发生反应的MAb进行了潜在中和活性测试;只有两种MAb抑制了A8病毒的增殖。这两种MAb对非嗜神经FLV株克隆57病毒无效或具有非常弱的中和活性。通过免疫沉淀对MAb进行进一步鉴定发现,有4种MAb识别A8病毒的包膜蛋白。这4种MAb中的两种识别表面糖蛋白gp70,这种识别需要病毒的构象表位,而另外两种与跨膜蛋白p15E发生反应的MAb则不依赖构象。两种针对gp70的MAb在一定程度上通过免疫沉淀检测到的中和活性或结合活性区分神经致病性和非神经致病性病毒,而两种针对p15E的MAb与病毒的反应方式相似。此外,其中一种MAb区分了由FrC6病毒感染大脑诱导形成海绵状病变的空泡壁中的病毒抗原。

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