Cambi F, Lees M B, Williams R M, Macklin W B
Ann Neurol. 1983 Mar;13(3):303-8. doi: 10.1002/ana.410130313.
A chronic experimental allergic encephalomyelitis (EAE) has been produced in rabbits sensitized with bovine white matter proteolipid apoprotein. Eleven of 12 animals developed clinical disease one to six months after immunization with a single dose of the apoprotein. The clinical course was characterized by posterior ataxia, flaccid paralysis progressing to spastic paralysis, and incontinence. Spontaneous relapses and remissions were observed in 3 rabbits. Histologically, acute and chronic encephalomyelitis accompanied by primary demyelination were observed. Serum antibody production, assayed by both an enzyme-linked immunosorbent assay and an electroblot procedure, did not correlate with either the clinical course or the histopathological findings. Delayed hypersensitivity to proteolipid apoprotein was observed in all rabbits prior to the onset of clinical signs. The data suggest that lymphocytes specifically sensitized to the proteolipid may be involved in the pathogenesis of the demyelination in chronic EAE.
用牛白质蛋白脂蛋白致敏的家兔已诱发慢性实验性变应性脑脊髓炎(EAE)。12只动物中有11只在单次注射该脂蛋白免疫后1至6个月出现临床疾病。临床病程的特征为后部共济失调、弛缓性麻痹进展为痉挛性麻痹以及大小便失禁。3只家兔出现自发缓解和复发。组织学上,观察到伴有原发性脱髓鞘的急性和慢性脑脊髓炎。通过酶联免疫吸附测定法和电印迹法检测的血清抗体产生与临床病程或组织病理学结果均无相关性。在临床症状出现之前,所有家兔均观察到对蛋白脂蛋白的迟发型超敏反应。数据表明,对蛋白脂蛋白特异性致敏的淋巴细胞可能参与慢性EAE脱髓鞘的发病机制。