Willcox N, Mautner V
J Immunol. 1976 Jan;116(1):25-9.
We have tested the two principal theories which explain the previous finding that small amounts of type-specific antibody to the adenovirus hexon can neutralize infectivity, whereas even large amounts of cross-reactive antibody do not. a) It has been suggested that the type-specific determinants are especially prominent in the virion. We have therefore measured the capacity of whole virus to bind appropriate antibodies, using a sensitive radioimmunoprecipitation (RIP) system. In fact, virions bound type-specific and cross-reactive antibodies impartially. Moreover, they bound both much less effectively than did free hexon or disrupted virus, suggesting that many of each kind of determinant are inaccessible in virions. b) It has been suggested that the type-specific determinants are confined to those hexons located next to the pentons, and that they are the targets for neutralizing antibody. We have therefore studied the antigenicity of peripentonal and nonamer hexons isolated from virions, and found that each possessed both kinds of determinants. Furthermore, these were present in the same proportion as in hexons purified from the soluble antigens in infected cells ("free hexons"). We concluded that the mechanism of neutralization by antibody is complicated, and that the type-specific determinants exposed on the virion must play a crucial role.
我们已经对两种主要理论进行了验证,这两种理论解释了之前的一项发现:少量针对腺病毒六邻体的型特异性抗体能够中和感染性,而即便大量的交叉反应抗体也不能。a) 有人提出型特异性决定簇在病毒粒子中格外突出。因此,我们使用灵敏的放射免疫沉淀(RIP)系统测定了完整病毒结合相应抗体的能力。事实上,病毒粒子对型特异性抗体和交叉反应抗体的结合并无偏向性。此外,它们的结合效率远低于游离的六邻体或裂解病毒,这表明病毒粒子中每种决定簇的许多位点都无法接近。b) 有人提出型特异性决定簇局限于位于五邻体旁边的那些六邻体,并且它们是中和抗体的作用靶点。因此,我们研究了从病毒粒子中分离出的五邻体周围和九聚体六邻体的抗原性,发现每种都含有这两种决定簇。此外,它们的比例与从感染细胞中的可溶性抗原纯化出的六邻体(“游离六邻体”)中的比例相同。我们得出结论,抗体中和的机制很复杂,并且病毒粒子上暴露的型特异性决定簇必定起着关键作用。