Emini E A, Kao S Y, Lewis A J, Crainic R, Wimmer E
J Virol. 1983 May;46(2):466-74. doi: 10.1128/JVI.46.2.466-474.1983.
Antibody-mediated poliovirus neutralization was studied by using a series of 13 monospecific neutralizing antibodies. These antibodies were found to recognize seven individual viral epitopes, several of which functionally overlap one another. Each epitope was capable of undergoing variation so that the variant virus was no longer capable of being neutralized by antibody directed against that epitope. The measured degree of variation for each site varied from -3.1 to -4.2 log10 variant PFU per wild-type PFU. Under nonsaturating but neutralizing conditions, the antibodies, with the exception of those directed to one specific epitope, failed to completely inhibit the virion's binding to the cell. Similarly, none of the neutralizing antibodies completely inhibited viral penetration, but all prevented virus-specific transcription. A strong correlation was established between the binding of each of the neutralizing antibodies, with one exception, to the virion and a significant shift in the virion's pI from 7.0 to ca. 4.0.
通过使用一系列13种单特异性中和抗体研究了抗体介导的脊髓灰质炎病毒中和作用。发现这些抗体识别7个单独的病毒表位,其中几个在功能上相互重叠。每个表位都能够发生变异,从而使变异病毒不再能够被针对该表位的抗体中和。每个位点的测量变异程度为每野生型PFU -3.1至-4.2 log10变异PFU。在非饱和但中和的条件下,除了针对一个特定表位的抗体外,其他抗体均未能完全抑制病毒粒子与细胞的结合。同样,没有一种中和抗体能完全抑制病毒穿透,但所有抗体都能阻止病毒特异性转录。除一种抗体外,每种中和抗体与病毒粒子的结合与病毒粒子的pI从7.0显著转变至约4.0之间建立了强相关性。