Inoue A, Koh C S, Yahikozawa H, Yanagisawa N, Yagita H, Ishihara Y, Kim B S
Department of Medicine (Neurology), Shinshu University School of Medicine, Asahi 3-1-1, Matsumoto 390, Japan.
Int Immunol. 1996 Jul;8(7):1001-8. doi: 10.1093/intimm/8.7.1001.
The levels of tumor necrosis factor (TNF)-alpha producing cells were analyzed in mice with Theiler's murine encephalomyelitis virus-induced demyelinating disease (TMEV-IDD). Using an ELISPOT assay, we demonstrate an increase in TNF-alpha producing cells in the spinal cords of TMEV-infected SJL/J mice, especially at an active disease stage. The numbers of TNF-alpha producing cells were extremely high in susceptible SJL/J mice compared with the numbers in resistant BALB/c and C57BL/6 mice. TNF-alpha producing cells were also immunohistochemically identified in active lesions of TMEV-IDD at acute as well as chronic stages. The percentage of TNF-alpha producing cells compared with the total number of cells isolated from spinal cords was higher in TMEV-infected SJL/J mice than resistant BALB/c and C57BL/6 mice. Correspondingly, the level of TNF-alpha was much higher in the culture supernatants of both infiltrating cells in the spinal cords and spleen cells from clinically affected animals than that from similarly treated resistant mice. Treatment of virus-infected mice with a mAb specific for TNF-alpha at the beginning of the onset of disease suppressed the development of the demyelinating disease. These findings suggest that TNF-alpha may play an important role in the pathogenicity of TMEV-IDD.
在感染泰勒氏鼠脑脊髓炎病毒诱发脱髓鞘疾病(TMEV-IDD)的小鼠中,分析了产生肿瘤坏死因子(TNF)-α的细胞水平。使用酶联免疫斑点分析(ELISPOT),我们证明在感染TMEV的SJL/J小鼠脊髓中,产生TNF-α的细胞增加,尤其是在疾病活跃期。与抗性BALB/c和C57BL/6小鼠相比,易感SJL/J小鼠中产生TNF-α的细胞数量极高。在TMEV-IDD的急性和慢性阶段的活动性病变中,也通过免疫组织化学鉴定出产生TNF-α的细胞。与从脊髓分离的细胞总数相比,感染TMEV的SJL/J小鼠中产生TNF-α的细胞百分比高于抗性BALB/c和C57BL/6小鼠。相应地,临床患病动物脊髓中的浸润细胞和脾细胞的培养上清液中TNF-α水平比同样处理的抗性小鼠高得多。在疾病发作开始时,用针对TNF-α的单克隆抗体治疗病毒感染的小鼠可抑制脱髓鞘疾病的发展。这些发现表明,TNF-α可能在TMEV-IDD的致病性中起重要作用。