Raine C S, Traugott U
Lab Invest. 1983 Mar;48(3):275-84.
Guinea pigs with long-standing chronic experimental autoimmune (allergic) encephalomyelitis were treated with myelin basic protein (MBP) alone in incomplete Freund's adjuvant or MBP in combination with a lipid hapten, galactocerebroside in incomplete Freund's adjuvant and studied for up to 26 months post-treatment. Animals which received MBP/galactocerebroside consistently displayed a long-lasting, marked, clinical improvement within 3 months post-treatment. Of 14 animals treated with MBP/galactocerebroside four have been sampled for light and electron microscopy. The central nervous systems of these animals displayed widespread remyelination and profound oligodendroglial proliferation. Some oligodendroglia appeared to be of recent origin. This structural recovery had occurred against a background of advanced gliosis and fibrosis. Treatment with MBP alone was associated with an initial period of stabilization, but after several months, relapsing activity and disease progression returned. It is suggested that after prolonged autoimmune demyelination, oligodendrocytes can proliferate in the presence of advanced scarring, that central nervous system remyelination can be effected, and that these findings have relevance to multiple sclerosis.
患有长期慢性实验性自身免疫性(过敏性)脑脊髓炎的豚鼠,分别接受单独在不完全弗氏佐剂中的髓鞘碱性蛋白(MBP)治疗,或在不完全弗氏佐剂中接受MBP与脂质半抗原半乳糖脑苷脂联合治疗,并在治疗后长达26个月进行观察。接受MBP/半乳糖脑苷脂治疗的动物在治疗后3个月内持续表现出长期、显著的临床改善。在接受MBP/半乳糖脑苷脂治疗的14只动物中,有4只已进行光镜和电镜检查取样。这些动物的中枢神经系统显示出广泛的髓鞘再生和显著的少突胶质细胞增殖。一些少突胶质细胞似乎是近期产生的。这种结构恢复是在严重胶质增生和纤维化的背景下发生的。单独用MBP治疗会有一个初期的病情稳定期,但几个月后,病情会复发并进展。提示在长期自身免疫性脱髓鞘后,少突胶质细胞可在严重瘢痕形成的情况下增殖,中枢神经系统可实现髓鞘再生,且这些发现与多发性硬化症有关。