Bach M K, Block K J, Austen K F
J Exp Med. 1971 Apr 1;133(4):772-84. doi: 10.1084/jem.133.4.772.
IgGa, in contrast to IgE, antibodies mediated the antigen-induced release of histamine from rat peritoneal mast cells without a requirement for a latent period and without the capacity to bind firmly to the target cell. Nonetheless, IgGa anti-DNP antibody interfered with the capacity of rat anti-N. brasiliensis antiserum rich in IgE antibodies to prepare the target cells for histamine release by worm antigen. Further, interaction of IgE antibody-prepared cells with IgGa anti-DNP antibody and DNP-BSA at 0 degrees C so as to achieve sterile activation, or at 30 degrees C to permit histamine release, inactivated such cells as determined by the subsequent failure to release histamine upon challenge with worm antigen. Thus, although IgE and IgGa antibodies are immunochemically distinct homologous immunoglobulins and exhibit different functional characteristics, their interaction at the target cell involves a common receptor and at least one common point in the pathway to the release of pharmacologic agents from the cell.
与IgE不同,IgGa抗体介导大鼠腹腔肥大细胞从抗原诱导释放组胺,无需潜伏期,也没有牢固结合靶细胞的能力。尽管如此,IgGa抗DNP抗体干扰了富含IgE抗体的大鼠抗巴西日圆线虫抗血清通过蠕虫抗原使靶细胞释放组胺的能力。此外,在0℃下,用IgGa抗DNP抗体和DNP-BSA与IgE抗体致敏的细胞相互作用以实现无菌激活,或在30℃下使其释放组胺,结果发现这些细胞随后在受到蠕虫抗原攻击时无法释放组胺,从而失去活性。因此,尽管IgE和IgGa抗体是免疫化学上不同的同源免疫球蛋白,且表现出不同的功能特性,但它们在靶细胞上的相互作用涉及一个共同的受体以及细胞释放药理介质途径中的至少一个共同点。