Bitar D M, Whitacre C C
Department of Medical Microbiology and Immunology, Ohio State University College of Medicine, Columbus 43210.
Cell Immunol. 1988 Apr 1;112(2):364-70. doi: 10.1016/0008-8749(88)90305-x.
The oral administration of myelin basic protein (MBP) to Lewis rats prior to an encephalitogenic challenge resulted in total inhibition or a significant delay in the onset of experimental autoimmune encephalomyelitis (EAE). In vitro lymphocyte proliferative responses to MBP were significantly decreased in MBP-fed rats when compared with vehicle-fed controls. Suppression of EAE and in vitro proliferative responses to MBP were observed to be antigen specific, since oral feeding of a control protein exerted no suppressive effect. Moreover, the specificity of MBP-induced oral tolerance was shown to be species specific, since feeding guinea pig MBP (GPMBP) or human MBP (HuMBP) induced protection only against a GPMBP or HuMBP challenge, respectively. Conversely, Lewis rats could not be orally tolerized to the self antigen rat MBP.
在致脑炎攻击前给Lewis大鼠口服髓鞘碱性蛋白(MBP),可完全抑制实验性自身免疫性脑脊髓炎(EAE)的发作或使其显著延迟。与喂食赋形剂的对照大鼠相比,喂食MBP的大鼠对MBP的体外淋巴细胞增殖反应显著降低。由于口服对照蛋白没有抑制作用,因此观察到EAE的抑制和对MBP的体外增殖反应具有抗原特异性。此外,MBP诱导的口服耐受性的特异性显示为物种特异性,因为喂食豚鼠MBP(GPMBP)或人MBP(HuMBP)分别仅诱导针对GPMBP或HuMBP攻击的保护作用。相反,Lewis大鼠不能通过口服耐受自身抗原大鼠MBP。