Zhang J, Medaer R, Stinissen P, Hafler D, Raus J
Multiple Sclerosis Research Unit, Dr. L. Willems Instituut, Diepenbeek, Belgium.
Science. 1993 Sep 10;261(5127):1451-4. doi: 10.1126/science.7690157.
Activated autoreactive T cells are potentially pathogenic and regulated by clonotypic networks. Experimental autoimmune diseases can be treated by inoculation with autoreactive T cells (T cell vaccination). In the present study, patients with multiple sclerosis were inoculated with irradiated myelin basic protein (MBP)-reactive T cells. T cell responses to the inoculates were induced to deplete circulating MBP-reactive T cells in the recipients. Regulatory T cell lines isolated from the recipients inhibited T cells used for vaccination. The cytotoxicity of the CD8+ T cell lines was restricted by major histocompatibility antigens. Thus, clonotypic interactions regulating autoreactive T cells in humans can be induced by T cell vaccination.
活化的自身反应性T细胞具有潜在致病性,并受克隆型网络调控。实验性自身免疫疾病可通过接种自身反应性T细胞(T细胞疫苗接种)进行治疗。在本研究中,对多发性硬化症患者接种经辐照的髓鞘碱性蛋白(MBP)反应性T细胞。诱导T细胞对接种物产生反应,以耗尽受体中循环的MBP反应性T细胞。从受体中分离出的调节性T细胞系抑制用于疫苗接种的T细胞。CD8 + T细胞系的细胞毒性受主要组织相容性抗原限制。因此,T细胞疫苗接种可诱导人类中调节自身反应性T细胞的克隆型相互作用。