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霍乱毒素对小鼠的免疫调节作用。

Immunomodulatory effects of cholera toxin in mice.

作者信息

Hussain A, Himeno K, Mayumi H, Kawamura I, Tsuru S, Nomoto K

机构信息

Department of Immunology, Kyushu University, Fukuoka, Japan.

出版信息

Nat Immun Cell Growth Regul. 1989;8(4):231-44.

PMID:2797014
Abstract

Immunomodulatory effects of cholera toxin (CT) were investigated in a murine model using various immunological parameters. C3H/HeN mice were injected with 2 micrograms of CT at various intervals (from 6 h to 21 days) before the immunological assays. Thymocytes were markedly decreased in their absolute number, and the phenotypes in such cells were clearly shifted from Thy1.2high+ PNAhigh+ to Thy1.2low+ PNAlow+ 2-4 days after the CT treatment. Spleen T cells were relatively increased, while surface IgM positive B cells were rather decreased. Natural killer activity and in vivo and in vitro cytotoxic T lymphocyte activity were markedly suppressed during the early stages after the CT treatment but recovered completely within 21 days. Mixed lymphocyte reaction was profoundly suppressed at least for the 1st week after the CT treatment. Furthermore, EL-4 tumor of C57BL/6 origin grew progressively and killed the recipient C3H mice when such tumor cells were inoculated 6 h after the CT treatment. On the contrary, a marked augmentation of direct (IgM) and indirect (IgG) plaque-forming cell responses to sheep red blood cells was seen after CT treatment. Delayed footpad reaction to SRBC was also augmented after CT treatment. As the mechanisms, both direct augmentation of CD4+ T cells and direct suppression of CD8+ T cells appeared to occur at a time due to the CT treatment. An indirect effect of CT through the release of the endogenous steroids was dismissed in the present study. Taken together, CT appears to have differential immunomodulatory effects on various immune effector cells through various mechanisms.

摘要

使用各种免疫学参数,在小鼠模型中研究了霍乱毒素(CT)的免疫调节作用。在进行免疫学检测前的不同时间间隔(从6小时到21天),给C3H/HeN小鼠注射2微克CT。CT处理后2 - 4天,胸腺细胞的绝对数量显著减少,且这些细胞的表型明显从Thy1.2高表达+ PNA高表达+转变为Thy1.2低表达+ PNA低表达+。脾脏T细胞相对增加,而表面IgM阳性B细胞则有所减少。CT处理后的早期阶段,自然杀伤活性以及体内和体外细胞毒性T淋巴细胞活性均受到显著抑制,但在21天内完全恢复。CT处理后的至少第1周,混合淋巴细胞反应受到严重抑制。此外,当在CT处理后6小时接种C57BL/6来源的EL - 4肿瘤细胞时,该肿瘤在受体C3H小鼠体内逐渐生长并导致小鼠死亡。相反,CT处理后,对绵羊红细胞的直接(IgM)和间接(IgG)空斑形成细胞反应显著增强。CT处理后,对SRBC的迟发型足垫反应也增强。作为机制,CT处理似乎同时导致CD4 + T细胞直接增加和CD8 + T细胞直接抑制。本研究排除了CT通过内源性类固醇释放产生的间接作用。综上所述,CT似乎通过多种机制对各种免疫效应细胞具有不同的免疫调节作用。

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