Prat M, Tato F, Tarone G, Comoglio P M
Immunology. 1980 Feb;39(2):179-85.
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.
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。