Bruck C, Rensonnet N, Portetelle D, Cleuter Y, Mammerickx M, Burny A, Mamoun R, Guillemain B, van der Maaten M J, Ghysdael J
Virology. 1984 Jul 15;136(1):20-31. doi: 10.1016/0042-6822(84)90244-7.
A panel of monoclonal antibodies to the bovine leukemia virus envelope glycoprotein (BLV gp51) has previously demonstrated the association of the biological activities of the virus (infectivity, syncytia induction) with three out of eight epitopes of gp51. In BLV-infected cells, the unglycosylated homolog of the precursor to the BLV envelope glycoproteins (gPr72env) is a 47,000-MW polypeptide. Immunoprecipitation studies with monoclonal antibodies show that the neutralizing antibody-inducing sites, although present in gPr72env, are not conserved in the 47,000-MW unglycosylated homolog. Finally, it is demonstrated that the neutralizing antibody-inducing sites of gp51 are subject to antigenic variation among BLV isolates of the same or different geographical origins.
一组针对牛白血病病毒包膜糖蛋白(BLV gp51)的单克隆抗体先前已证明,该病毒的生物活性(感染性、合胞体诱导)与gp51的八个表位中的三个相关。在感染BLV的细胞中,BLV包膜糖蛋白前体(gPr72env)的未糖基化同源物是一种47,000道尔顿的多肽。用单克隆抗体进行的免疫沉淀研究表明,诱导中和抗体的位点虽然存在于gPr72env中,但在47,000道尔顿的未糖基化同源物中并不保守。最后,证明了gp51的诱导中和抗体的位点在相同或不同地理来源的BLV分离株之间存在抗原变异。