Abraham G N, Welch E, Trieshmann H W
Immunology. 1978 Sep;35(3):437-45.
The specificity and reactivity patterns of monoclonal IgG, IgA and IgM anti-IgG autoantibodies isolated from the serum of one patient (Gil) have been determined for IgGs of the four gamma chain subclasses. The haemagglutination produced by the interaction of the Gil anti-IgGs and anti-Rh IgG coated erythrocytes was inhibited by a panel of intact IgGs, their polypeptide chains, and enzymatic fragments which included purified heavy chain constant region domains. Intact IgG1, IgG2, and IgG4 produced the same patterns of reactivity with the Gil anti-IgGs. When partially reduced and alkylated IgG1 heavy chains and its tryptic digests were tested, these were much more reactive than Fc fragments isolated from IgG of the four subclasses which were weaker inhibitors, and gamma chain constant region domains which were totally non-reactive. In all instances and by use of two anti-Rh antisera, the specificity patterns obtained for the Gil anti-IgGs were identical. The data combined with previous knowledge of the identity of the Gil light chains suggests that the antibody combining sites of these molecules are very similar if not identical.
已测定从一名患者(吉尔)血清中分离出的单克隆IgG、IgA和IgM抗IgG自身抗体针对四种γ链亚类IgG的特异性和反应模式。吉尔抗IgG与抗Rh IgG包被红细胞相互作用产生的血凝反应受到一组完整IgG、其多肽链和酶切片段(包括纯化的重链恒定区结构域)的抑制。完整的IgG1、IgG2和IgG4与吉尔抗IgG产生相同的反应模式。当测试部分还原和烷基化的IgG1重链及其胰蛋白酶消化产物时,它们的反应性比从四种亚类IgG中分离出的Fc片段(较弱的抑制剂)和完全无反应性的γ链恒定区结构域高得多。在所有情况下,使用两种抗Rh抗血清,吉尔抗IgG获得的特异性模式均相同。这些数据与之前关于吉尔轻链身份的知识相结合,表明这些分子的抗体结合位点即使不完全相同也非常相似。