Lifke V V, Razumov I A, Konovalova S N
Vopr Virusol. 1997 Jan-Feb;42(1):19-23.
A panel of 9 mouse hybridomas producing monoclonal antibodies (MAb-2) to determinants of rat MAb 4H5 (MAb-1) was prepared. MAb-1 blocked hemagglutination caused by different alphaviruses. The specificity of paratopes of MAb-2 was studied by competitive enzyme immunoassay and they were divided into 2 groups: 1) interacting with isotypic and/or allotypic determinants of molecules of MAb 4H5 (5 hybridomas) and 2) specific to idiotypic determinants of MAb 4H5 molecules (4 hybridomas). The antigenic structure of paratopes of 3 antiidiotypic MAb (1C2, 1F9, and 6C8) was specific to the idiotopes localized in the active MAb 4H5 center interacting with the hemagglutination domain of VEE virus glycoprotein E2. These antiidiotypic MAb can agglutinate goose red cells, this indicating that the antigenic structure of their paratopes mimicks the functional determinant of the hemagglutination domain of VEE virus glycoprotein E2.
制备了一组9个小鼠杂交瘤,它们产生针对大鼠单克隆抗体4H5(MAb-1)决定簇的单克隆抗体(MAb-2)。MAb-1可阻断由不同甲病毒引起的血凝反应。通过竞争性酶免疫测定法研究了MAb-2互补位的特异性,它们被分为2组:1)与MAb 4H5分子的同种型和/或异型决定簇相互作用(5个杂交瘤),2)对MAb 4H5分子的独特型决定簇具有特异性(4个杂交瘤)。3种抗独特型单克隆抗体(1C2、1F9和6C8)的互补位抗原结构对位于与委内瑞拉马脑炎病毒糖蛋白E2血凝结构域相互作用的活性MAb 4H5中心的独特位具有特异性。这些抗独特型单克隆抗体可凝集鹅红细胞,这表明它们互补位的抗原结构模拟了委内瑞拉马脑炎病毒糖蛋白E2血凝结构域的功能决定簇。