Abramsky O, Brenner T, Mizrachi R, Soffer D
J Neuroimmunol. 1982 Jan;2(1):1-7. doi: 10.1016/0165-5728(82)90070-4.
Experimental allergic encephalomyelitis (EAE), induced in guinea pigs by immunization with myelin basic protein (MBP) or whole CNS homogenate was successfully treated, as well as partially prevented, by daily administration of fetal alpha-fetoprotein (alpha FP). alpha FP which is produced in high quantities during pregnancy can inhibit both the cell-mediated immune response to MBP and the binding of MBP antibody to the antigen in vitro. It has a non-specific immunosuppressive effect on both the cellular and humoral responses. It is suggested that the ability of alpha FP to suppress an experimental autoimmune disease, as presented in this model of EAE, indicates that clinical remissions of human autoimmune disease during pregnancy may be attributed to the effect of this natural substance.
通过用髓鞘碱性蛋白(MBP)或全中枢神经系统匀浆免疫豚鼠诱导出实验性变应性脑脊髓炎(EAE),每日给予胎甲球蛋白(αFP)可成功治疗该疾病,并能部分预防。在怀孕期间大量产生的αFP在体外既能抑制对MBP的细胞介导免疫反应,又能抑制MBP抗体与抗原的结合。它对细胞和体液反应均有非特异性免疫抑制作用。有人提出,如在该EAE模型中所示,αFP抑制实验性自身免疫疾病的能力表明,人类自身免疫疾病在怀孕期间的临床缓解可能归因于这种天然物质的作用。