Traugott U, Stone S H, Raine C S
J Neurol Sci. 1979 Mar;41(1):17-29. doi: 10.1016/0022-510x(79)90136-9.
Groups of juvenile Strain 13 guinea pigs sensitized for chronic relapsing experimental allergic encephalomyelitis (EAE) with isogeneic central nervous system (CNS) tissue in complete Freund's adjuvant (CFA) were either left to develop late-onset chronic EAE (unsuppressed), or given a series of injections of bovine myelin basic protein (MBP) in incomplete Freund's adjuvant (IFA) to suppress the disease. All unsuppressed animals developed disease and all suppressed animals remained healthy over a 27-month period of study. some unsuppressed and suppressed animals were rechallenged with CNS tissue in CFA 12 or 26 months post-inoculation (PI). Unsuppressed animals all became sick 2-4 weeks after rechallenge, while rechallenged, suppressed animals were protected, indicating that the suppression was permanent. Pathologic findings in the CNS complemented the clinical changes. Circulating lymphocyte studies were performed on animals from all groups. Early (active, high-affinity rosetting) T cell levels in unsuppressed animals showed significant decreases during exacerbations (P less than 0.01) and normal values during remissions. After rechallenge, circulating early T cells decreased in unsuppressed animals with the development of signs. In suppressed animals, early T cells showed significant elevations during, and for a short time after, the period of suppressive injections, and normal values afterwards. These levels did not change significantly after rechallenge. Late (total, 24 hour rosetting) T cell and B cell values showed minor fluctuations only which did not correlate with disease activity. These results indicate that chronic relapsing EAE can be successfully suppressed with MBP in IFA, that this suppression is permanent and that the immunologic findings presented correlate well with the clinical and pathologic facets of the disease. the findings are presented in terms of their relevance to multiple sclerosis.
将同基因中枢神经系统(CNS)组织与完全弗氏佐剂(CFA)一起用于致敏,以诱发慢性复发性实验性变态反应性脑脊髓炎(EAE)的幼年13号品系豚鼠,被分为两组,一组任其发展为迟发性慢性EAE(未抑制组),另一组则给予一系列牛髓鞘碱性蛋白(MBP)与不完全弗氏佐剂(IFA)的注射以抑制疾病。在为期27个月的研究期间,所有未抑制组的动物都发病了,而所有抑制组的动物都保持健康。一些未抑制组和抑制组的动物在接种后(PI)12或26个月,再次用CFA中的CNS组织进行攻击。未抑制组的动物在再次攻击后2 - 4周全部发病,而再次攻击的抑制组动物受到了保护,这表明抑制是永久性的。CNS中的病理发现与临床变化相符合。对所有组的动物进行了循环淋巴细胞研究。未抑制组动物早期(活性、高亲和力玫瑰花结形成)T细胞水平在病情加重期间显著下降(P小于0.01),缓解期则为正常值。再次攻击后,出现症状的未抑制组动物循环早期T细胞减少。在抑制组动物中,早期T细胞在抑制性注射期间及之后短时间内显著升高,之后恢复正常水平。再次再次攻击后这些水平没有明显变化。晚期(总、24小时玫瑰花结形成)T细胞和B细胞值仅显示微小波动,与疾病活动无关。这些结果表明,用IFA中的MBP可以成功抑制慢性复发性EAE,这种抑制是永久性的,并且所呈现的免疫学发现与该疾病的临床和病理方面密切相关。这些发现是根据它们与多发性硬化症的相关性来呈现的。