Stevenson F K, Elliott E V, Stevenson G T
Immunology. 1977 Apr;32(4):549-57.
During the growth of the L2C leukaemia in strain 2 guinea-pigs there is excreted in the urine a monoclonal light chain of lambda class. This is believed to arise from synthesis by the leukaemic cells of a small molar excess of the light chains incorporated into their surface IgM. Antibodies to this light chain have been raised in rabbits and separated by immunosorption into those directed against idiotypic determinants (anti-Id), and those against determinants also present on other lambda chains (anti-lambda). Both antibodies react with L2C cells via the surface immunoglobulin. In accord with prediction anti-Id is specific for L2C cells while anti-lambda also reacts with 7 per cent of normal nodal lymphocytes. L2C cells are agglutinated strongly by anti-Id, weakly by anti-lambda. Both antisera inhibit migration of the cells, and both can kill them by invoking complement or K-cell cytotoxic mechanisms. The results emphasize the potential of anti-idiotype sera for identifying and specifically attacking neoplastic B lymphocytes.
在2系豚鼠中L2C白血病生长期间,尿液中会排泄出一种λ类单克隆轻链。据信这是由白血病细胞合成的,其合成的轻链摩尔数略多于整合到其表面IgM中的轻链。针对这种轻链的抗体已在兔中产生,并通过免疫吸附分离为针对独特型决定簇的抗体(抗独特型)和针对其他λ链上也存在的决定簇的抗体(抗λ)。两种抗体都通过表面免疫球蛋白与L2C细胞发生反应。与预测一致,抗独特型对L2C细胞具有特异性,而抗λ也与7%的正常淋巴结淋巴细胞发生反应。L2C细胞被抗独特型强烈凝集,被抗λ微弱凝集。两种抗血清均抑制细胞迁移,并且都可以通过激活补体或K细胞细胞毒性机制杀死它们。结果强调了抗独特型血清在识别和特异性攻击肿瘤性B淋巴细胞方面的潜力。