Pierres M, Ju S T, Waltenbaugh C, Dorf M E, Benacerraf B, Germain R N
Proc Natl Acad Sci U S A. 1979 May;76(5):2425-9. doi: 10.1073/pnas.76.5.2425.
The polyethylene glycol-mediated cell fusion technique has been used to analyze the diversity of the antibody response to the terpolymer poly(Glu60Ala30Tyr10)(GAT). Nine stable clones (all producing IgM K anti-GAT antibodies) were isolated from a fusion between P3-X63-Ag8 myeloma cells and spleen cells from a DBA/2 mouse sensitized to GAT 5 days earlier. Seven other clones (producing IgG K anti-GAT antibodies) were derived from another fusion between NSI myeloma cells and spleen cells of (C57BL/6 X DBA/2)F1 hybrid mice hyperimmunized with GAT. These 16 anti-GAT antibodies were grouped according to their pattern of reactivity with GAT and the two related polymers of poly(Glu60Ala40) (GA) and poly(GLU50Tyr50) (GT). Two monoclonal anti-GAT antibodies (IgM F9-102.2 and IgG F17-148.3) demonstrated crossreactivity with GA but failed to crossreact with GT determinants. In contrast, the remaining 14 hybridoma antibodies demonstrated preferential reactivity with GAT but also exhibited crossreactive binding to GT and in some cases GA. There was a correlation between the fine specificity pattern and the presence of a common anti-GAT idiotype on these antibodies. Thus, the hybridoma anti-GAT antibodies which reacted with GT shared crossreactive idiotypic determinants (CGAT) present in mouse anti-GAT immune sera. In contrast, the monoclonal F9-102.2 and F17-148.3 antibodies that failed to bind to GT lacked the major CGAT idiotypic determinants.
聚乙二醇介导的细胞融合技术已被用于分析针对三元共聚物聚(Glu60Ala30Tyr10)(GAT)的抗体反应多样性。从5天前对GAT致敏的DBA/2小鼠的脾脏细胞与P3-X63-Ag8骨髓瘤细胞的融合物中分离出9个稳定克隆(均产生IgM κ抗GAT抗体)。另外7个克隆(产生IgG κ抗GAT抗体)来自NSI骨髓瘤细胞与用GAT超免疫的(C57BL/6×DBA/2)F1杂种小鼠的脾脏细胞之间的另一次融合。根据这16种抗GAT抗体与GAT以及聚(Glu60Ala40)(GA)和聚(GLU50Tyr50)(GT)这两种相关聚合物的反应模式进行分组。两种单克隆抗GAT抗体(IgM F9-102.2和IgG F17-148.3)与GA表现出交叉反应,但与GT决定簇无交叉反应。相比之下,其余14种杂交瘤抗体对GAT表现出优先反应性,但也与GT以及在某些情况下与GA表现出交叉反应性结合。这些抗体的精细特异性模式与共同抗GAT独特型的存在之间存在相关性。因此,与GT反应的杂交瘤抗GAT抗体共享存在于小鼠抗GAT免疫血清中的交叉反应性独特型决定簇(CGAT)。相比之下,未能与GT结合的单克隆F9-102.2和F17-148.3抗体缺乏主要的CGAT独特型决定簇。