Hallam T J
Roche Research Centre, Welwyn Garden City, Herts, U.K.
Clin Exp Rheumatol. 1993 Mar-Apr;11 Suppl 8:S131-4.
The assumption that protein kinase C activation is necessary for T-cell activation in response to MHC class II restricted antigen-presentation is supported by several lines of circumstantial evidence. We have developed potent, cell-permeable and selective inhibitors of PKC to test this hypothesis. Our data demonstrate the crucial role for PKC in T-cell activation and that selective orally bioavailable PKC inhibitors are efficacious in preventing T-cell driven chronic inflammatory responses in vivo.
有几条间接证据支持这样一种假设,即蛋白激酶C激活对于T细胞响应MHC II类限制性抗原呈递而活化是必要的。我们已经开发出了有效的、可穿透细胞的蛋白激酶C选择性抑制剂来验证这一假设。我们的数据证明了蛋白激酶C在T细胞活化中的关键作用,并且选择性口服生物可利用的蛋白激酶C抑制剂在体内预防T细胞驱动的慢性炎症反应方面是有效的。