Wiley J A, Hamel J, Brodeur B R
National Laboratory for Immunology, Laboratory Center for Disease Control, Ottawa, Ontario, Canada.
J Virol. 1992 Oct;66(10):5744-51. doi: 10.1128/JVI.66.10.5744-5751.1992.
Monoclonal antibodies (MAbs) directed against the prototype enterovirus 70 (EV-70) strain J670/71 were generated and characterized in order to produce anti-idiotypic MAbs (MAb2s) for use as surrogate immunogens. Western immunoblot and radioimmunoprecipitation assays suggested that all the MAbs recognize conformational epitopes on the virion surface. An EV-70-neutralizing antibody, MAb/ev-12 (MAb1), was selected for the production of MAb2s. Five MAb2s were selected for their capacities to inhibit the interaction of MAb/ev-12 with EV-70 in dot immunobinding inhibition and immunofluorescence assays. In addition, these five MAb2s inhibited virus neutralization mediated by MAb/ev-12, suggesting that they recognize paratope-associated idiotopes. In competition enzyme immunosorbent assays, none of the five MAb2s recognized other neutralizing and nonneutralizing EV-70-specific MAbs, demonstrating that the MAb2s were specific for private idiotopes. Immunization with each of the MAb2s was carried out for the production of anti-anti-idiotypic antibodies (Ab3). All five MAb2s induced an immune response. Moreover, results suggested that they share idiotopes, since MAb2-MAb/ev-12 binding could be inhibited by homologous as well as heterologous Ab3s. Ab3 sera were shown to possess antibodies capable of immunoprecipitating 35S-labeled viral proteins in the same manner as MAb/ev-12. Nine of 15 mice immunized with MAb2s demonstrated Ab3 neutralizing activity specific for the prototype EV-70 strain, J670/71. The potential application of MAb2s to serve as surrogate immunogens for conformational epitopes is substantiated by the results presented in this report.
为了生产用作替代免疫原的抗独特型单克隆抗体(MAb2),制备并鉴定了针对原型肠道病毒70型(EV - 70)毒株J670/71的单克隆抗体(MAb)。蛋白质免疫印迹和放射免疫沉淀试验表明,所有单克隆抗体均识别病毒粒子表面的构象表位。选择一种EV - 70中和抗体MAb/ev - 12(MAb1)来制备MAb2。在斑点免疫结合抑制试验和免疫荧光试验中,根据五种MAb2抑制MAb/ev - 12与EV - 70相互作用的能力对其进行筛选。此外,这五种MAb2抑制了MAb/ev - 12介导的病毒中和作用,表明它们识别与互补位相关的独特型表位。在竞争酶联免疫吸附试验中,这五种MAb2均未识别其他中和及非中和的EV - 70特异性单克隆抗体,表明这些MAb2对个体独特型表位具有特异性。用每种MAb2进行免疫以产生抗抗独特型抗体(Ab3)。所有五种MAb2均诱导了免疫反应。此外,结果表明它们共享独特型表位,因为同源及异源Ab3均可抑制MAb2与MAb/ev - 12的结合。Ab3血清显示具有能够以与MAb/ev - 12相同方式免疫沉淀35S标记病毒蛋白的抗体。用MAb2免疫的15只小鼠中有9只表现出对原型EV - 70毒株J670/71具有特异性的Ab3中和活性。本报告中的结果证实了MAb2用作构象表位替代免疫原的潜在应用价值。