Hirayama M, Lisak R P, Silberberg D H
Neurology. 1986 Feb;36(2):276-8. doi: 10.1212/wnl.36.2.276.
We examined serum-mediated cytotoxicity on cultured rat oligodendrocytes, using serum from patients with acute or chronic progressive multiple sclerosis and normal controls. We found heat-labile serum factors in serum from MS and also in controls. The cytotoxic effects of MS and normal sera were not restored by adding a source of complement. Despite apparent lack of disease specificity, such factors might damage oligodendrocytes if they gained access to these cells through a damaged blood-brain barrier in MS or other disorders.
我们使用急性或慢性进行性多发性硬化症患者及正常对照者的血清,检测了血清介导的对培养大鼠少突胶质细胞的细胞毒性。我们在多发性硬化症患者血清以及对照血清中均发现了热不稳定血清因子。添加补体来源并不能恢复多发性硬化症血清和正常血清的细胞毒性作用。尽管明显缺乏疾病特异性,但如果这些因子通过多发性硬化症或其他疾病中受损的血脑屏障进入这些细胞,可能会损害少突胶质细胞。