Uchigata Y, Takayama-Hasumi S, Kawanishi K, Hirata Y
Diabetes Centre, Tokyo Women's Medical College, Japan.
Diabetes. 1991 Aug;40(8):966-70. doi: 10.2337/diab.40.8.966.
We previously showed that purified human IgG1 insulin autoantibody (IAA) from the serum of male patient T.H. with insulin autoimmune syndrome is directed at a determinant at the asparagine site on the human insulin B chain. An anti-idiotypic antibody (anti-TH) that inhibited TH-IAA binding to human insulin was obtained by immunizing BALB/c mice with TH-IAA. Anti-TH bound to viable IM-9 cells and the purified insulin receptor from IM-9 cells. Anti-TH binding to IM-9 cells and the insulin receptor was inhibited by TH-IAA but not by human IgG. Moreover, incubation of HepG2 cells with anti-TH had an inhibitory effect on insulin binding to HepG2 cells. Anti-TH, like insulin, stimulated amino acid uptake in HepG2 cells. These findings indicate that the conformation of TH-IAA idiotope is a mirror image of the determinant on the insulin B chain, the binding site for TH-IAA on anti-TH is also related to the insulin binding site on the insulin receptor, and anti-TH mimics insulin action on the insulin receptor.
我们先前表明,从患有胰岛素自身免疫综合征的男性患者T.H.血清中纯化的人IgG1胰岛素自身抗体(IAA)针对人胰岛素B链天冬酰胺位点的一个决定簇。通过用TH-IAA免疫BALB/c小鼠,获得了一种抑制TH-IAA与人胰岛素结合的抗独特型抗体(抗-TH)。抗-TH与存活的IM-9细胞以及来自IM-9细胞的纯化胰岛素受体结合。TH-IAA可抑制抗-TH与IM-9细胞和胰岛素受体的结合,而人IgG则无此作用。此外,用抗-TH孵育HepG2细胞对胰岛素与HepG2细胞的结合有抑制作用。抗-TH与胰岛素一样,可刺激HepG2细胞摄取氨基酸。这些发现表明,TH-IAA独特型表位的构象是胰岛素B链上决定簇的镜像,抗-TH上TH-IAA的结合位点也与胰岛素受体上的胰岛素结合位点相关,并且抗-TH模拟了胰岛素对胰岛素受体的作用。