Genain C P, Cannella B, Hauser S L, Raine C S
Department of Neurology, University of California, San Francisco 94143-0435, USA.
Nat Med. 1999 Feb;5(2):170-5. doi: 10.1038/5532.
The molecular mechanisms underlying myelin sheath destruction in multiple sclerosis lesions remain unresolved. With immunogold-labeled peptides of myelin antigens and high-resolution microscopy, techniques that can detect antigen-specific antibodies in situ, we have identified autoantibodies specific for the central nervous system myelin antigen myelin/oligodendrocyte glycoprotein. These autoantibodies were specifically bound to disintegrating myelin around axons in lesions of acute multiple sclerosis and the marmoset model of allergic encephalomyelitis. These findings represent direct evidence that autoantibodies against a specific myelin protein mediate target membrane damage in central nervous system demyelinating disease.
多发性硬化症病变中髓鞘破坏的分子机制尚未明确。利用髓鞘抗原的免疫金标记肽和高分辨率显微镜技术(可原位检测抗原特异性抗体),我们鉴定出了针对中枢神经系统髓鞘抗原髓鞘/少突胶质细胞糖蛋白的自身抗体。这些自身抗体特异性结合于急性多发性硬化症病变及狨猴变应性脑脊髓炎模型中轴突周围正在崩解的髓鞘。这些发现代表了直接证据,即针对特定髓鞘蛋白的自身抗体介导中枢神经系统脱髓鞘疾病中的靶膜损伤。