Sairenji T, Bertoni G, Medveczky M M, Medveczky P G, Nguyen Q V, Humphreys R E
Department of Pharmacology, University of Massachusetts Medical School, Worcester 01655.
J Virol. 1988 Aug;62(8):2614-21. doi: 10.1128/JVI.62.8.2614-2621.1988.
Antibody-mediated inhibition of Epstein-Barr virus (EBV) release from the EBV-productive cell lines P3HR-1 and B95-8 was probed with two monoclonal antibodies (MAbs), 72A1 and 2L10, which immunoprecipitated the same EBV membrane antigen (MA) gp350/220 found with the 1B6 MAb with which inhibition of EBV release from P3HR-1 cells was first described. These three MAbs were not equivalent in either MA reactivities or functional effects, reflecting the variable expression of different epitopes of gp350/220. 1B6 recognized MA on P3HR-1 cells, which expressed predominately the gp220 form of MA. 1B6 did not recognize (or barely recognized) a determinant on B95-8 cells. MAbs 2L10 and 72A1 reacted as well with B95-8 cells as they did with P3HR-1 cells. MAbs 1B6 and 2L10 neutralized neither P3HR-1 nor B95-8 virus, but 72A1 neutralized both viruses. MAbs 1B6 and 72A1 inhibited P3HR-1 virus release, as measured by the assay for infectious virus and by DNA hybridization analysis of released virus, but 2L10 had no such activity. 72A1 (but not 1B6) inhibited release of EBV from B95-8 cells. These experiments pointed to the presence of three different epitopes on gp350/220, identified with the respective MAbs and having varying involvement in virus neutralization and virus release inhibition.
用两种单克隆抗体(MAb)72A1和2L10探究抗体介导的对爱泼斯坦-巴尔病毒(EBV)从产生EBV的细胞系P3HR-1和B95-8中释放的抑制作用。这两种单克隆抗体免疫沉淀出与1B6单克隆抗体所识别的相同的EBV膜抗原(MA)gp350/220,首次报道1B6单克隆抗体可抑制EBV从P3HR-1细胞中释放。这三种单克隆抗体在MA反应性或功能效应方面并不等同,这反映了gp350/220不同表位的可变表达。1B6识别P3HR-1细胞上的MA,该细胞主要表达MA的gp220形式。1B6不能识别(或几乎不能识别)B95-8细胞上的一个决定簇。单克隆抗体2L10和72A1与B95-8细胞的反应和它们与P3HR-1细胞的反应一样好。单克隆抗体1B6和2L10既不能中和P3HR-1病毒也不能中和B95-8病毒,但72A1能中和这两种病毒。通过感染性病毒检测和对释放病毒的DNA杂交分析测定,单克隆抗体1B6和72A1可抑制P3HR-1病毒的释放,但2L10没有这种活性。72A1(而非1B6)可抑制EBV从B95-8细胞中释放。这些实验表明gp350/220上存在三种不同的表位,分别由相应的单克隆抗体识别,并且它们在病毒中和及病毒释放抑制中所起的作用各不相同。