Koike T, Itoh Y, Ishii T, Ito I, Takabayashi K, Maruyama N, Tomioka H, Yoshida S
Diabetes. 1987 Apr;36(4):539-41. doi: 10.2337/diab.36.4.539.
We analyzed the surface phenotypes of infiltrated cells in pancreases of nonobese diabetic (NOD) mice with monoclonal antibodies to mouse lymphocytes. Most of the infiltrated cells were Thy1+ and Ly1+ T-lymphocytes, and most of them were L3T4+ helper T-lymphocyte subsets. To elucidate the role of L3T4+ T-lymphocytes in the development of insulitis and diabetes in NOD mice, we treated the animals with injections of monoclonal anti-L3T4 antibody. Administration of this antibody prevented the insulitis and diabetes in NOD mice. These results lead to conclusions that the L3T4+ helper T-lymphocytes may play an essential role in the pathogenesis of type I diabetes and that the manipulation of the OKT4+ (Leu3+) T-lymphocyte subset, the human homology of L3T4, with monoclonal antibodies may provide effective therapy for human type I diabetes.
我们用针对小鼠淋巴细胞的单克隆抗体分析了非肥胖糖尿病(NOD)小鼠胰腺中浸润细胞的表面表型。大多数浸润细胞是Thy1+和Ly1+ T淋巴细胞,其中大多数是L3T4+辅助性T淋巴细胞亚群。为了阐明L3T4+ T淋巴细胞在NOD小鼠胰岛炎和糖尿病发生发展中的作用,我们给动物注射单克隆抗L3T4抗体进行治疗。给予这种抗体可预防NOD小鼠的胰岛炎和糖尿病。这些结果得出结论,L3T4+辅助性T淋巴细胞可能在I型糖尿病发病机制中起重要作用,并且用单克隆抗体操纵与L3T4具有人类同源性的OKT4+(Leu3+)T淋巴细胞亚群可能为人类I型糖尿病提供有效治疗。