de Berardinis P, Londei M, James R F, Lake S P, Wise P H, Feldmann M
Charing Cross Sunley Research Centre, London.
Lancet. 1988 Oct 8;2(8615):823-4. doi: 10.1016/s0140-6736(88)92785-7.
The mechanism by which islet beta cells are destroyed in type 1 diabetes is still unknown. Because in diabetes the majority of T cells activated in vivo express CD4 and the islet beta cells selectively express the HLA class II antigens needed for recognition by CD4-positive T cells, the possibility that selective damage to islet beta cells may be caused by CD4-positive cytotoxic cells was investigated. Activated T cells were cloned from a newly diagnosed diabetic patient, and many CD4 cytotoxic clones were detected. The clone with the highest cytolytic capacity lysed HLA class II compatible islet cells which had been induced by interferon gamma and tumour necrosis factor to express class II antigens. The specificity of the lysis was demonstrated by use of histoincompatible islets, other histocompatible target cells, and blocking by anti-class-II monoclonal antibodies. The results show that a CD4-positive T cell clone can lyse HLA class II matched islet cells; this process may be important in the pathogenesis of type 1 diabetes.
1型糖尿病中胰岛β细胞被破坏的机制仍不清楚。由于在糖尿病中,体内激活的大多数T细胞表达CD4,且胰岛β细胞选择性表达CD4阳性T细胞识别所需的HLA II类抗原,因此研究了CD4阳性细胞毒性细胞可能导致胰岛β细胞选择性损伤的可能性。从一名新诊断的糖尿病患者中克隆出活化的T细胞,并检测到许多CD4细胞毒性克隆。细胞溶解能力最强的克隆可裂解由干扰素γ和肿瘤坏死因子诱导表达II类抗原的HLA II类相容胰岛细胞。通过使用组织不相容的胰岛、其他组织相容性靶细胞以及抗II类单克隆抗体的阻断作用,证明了这种裂解的特异性。结果表明,CD4阳性T细胞克隆可裂解HLA II类匹配的胰岛细胞;这一过程在1型糖尿病的发病机制中可能很重要。