Pierce J W, Hudak S, Claflin J L
Mol Immunol. 1984 Feb;21(2):159-66. doi: 10.1016/0161-5890(84)90131-7.
The immune response to phosphocholine (PC) in mice is highly restricted. Most anti-PC antibodies use heavy-chain variable-region (VH) sequences derived from single VH gene segment, V1. In order to investigate whether a highly homologous VH gene segment, V11, could contribute to the formation of PC-binding antibodies, we carried out chain recombination experiments with M47A, a non-PC binding myeloma protein whose H-chain is encoded by the V11 gene segment, and two PC-binding antibodies, HP101.6G6 (HP6G6) and M511. The H-chains from the non-PC-binding myeloma protein, M47A, formed a functional PC-binding site when paired with L-chains from both PC-binding antibodies. These results suggest that a second VH gene segment, V11, could theoretically be used to form PC-binding antibodies. In addition, these results provide direct evidence that a single H-chain can be used in combinatorial association with different L-chains to form antibodies of differing specificities.
小鼠对磷酸胆碱(PC)的免疫反应受到高度限制。大多数抗PC抗体使用源自单个重链可变区(VH)基因片段V1的序列。为了研究高度同源的VH基因片段V11是否有助于PC结合抗体的形成,我们用M47A进行了链重组实验,M47A是一种非PC结合骨髓瘤蛋白,其重链由V11基因片段编码,以及两种PC结合抗体HP101.6G6(HP6G6)和M511。当与来自两种PC结合抗体的轻链配对时,非PC结合骨髓瘤蛋白M47A的重链形成了功能性PC结合位点。这些结果表明,第二个VH基因片段V11理论上可用于形成PC结合抗体。此外,这些结果提供了直接证据,即单个重链可与不同轻链组合结合,形成具有不同特异性的抗体。