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呼吸道合胞病毒转化的成纤维细胞表面作为抗体和补体作用靶点的抗原。

Target antigens for antibodies and complement at the cell surface of RSV-transformed fibroblasts.

作者信息

Prat M, Tato F, Tarone G, Comoglio P M

出版信息

Immunology. 1980 Feb;39(2):179-85.

Abstract

Using cells transformed by Rous sarcoma virus (RSV), an RNA tumour virus whose genetic and structural composition is fully known, the virus-induced surface antigens acting as targets for antibodies and complement were studied. Among the virus structural proteins, only the envelope antigen gp85, but not the core group-specific proteins or reverse transcriptase, were able to mediate immune lysis in the 51Cr-release assay. The group-specific antigenic determinants of gp85 were predominantly involved. The virus-induced cell surface antigen (VCSA), specific for transformation, was the only other molecule effective. Since different cells express either of these antigens, further support is given to the non-identity of virus structural antigens and VCSA.

摘要

利用经劳斯肉瘤病毒(RSV)转化的细胞,该病毒是一种遗传和结构组成完全已知的RNA肿瘤病毒,对作为抗体和补体靶标的病毒诱导表面抗原进行了研究。在病毒结构蛋白中,只有包膜抗原gp85,而不是核心群特异性蛋白或逆转录酶,能够在51Cr释放试验中介导免疫裂解。gp85的群特异性抗原决定簇起主要作用。病毒诱导的细胞表面抗原(VCSA),对转化具有特异性,是唯一有效的其他分子。由于不同细胞表达这些抗原中的一种,这进一步支持了病毒结构抗原和VCSA的非同一性。

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