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用CD4特异性单克隆抗体处理的小鼠,对淋巴细胞性脉络丛脑膜炎病毒和痘苗病毒产生抗病毒细胞毒性的能力受损。

Impaired generation of anti-viral cytotoxicity against lymphocytic choriomeningitis and vaccinia virus in mice treated with CD4-specific monoclonal antibody.

作者信息

Leist T P, Kohler M, Zinkernagel R M

机构信息

Institute for Pathology, University Hospital, Zurich, Switzerland.

出版信息

Scand J Immunol. 1989 Dec;30(6):679-86. doi: 10.1111/j.1365-3083.1989.tb02476.x.

Abstract

The role of CD4+ helper T cells in induction of anti-viral cytotoxic T-cell response was investigated by treating normal and thymectomized C57B1/6 mice with CD4-specific monoclonal antibodies (MoAb). In CD4-specific MoAb-treated mice infected with Vaccinia or lymphocytic choriomeningitis virus (LCMV), cytotoxic T-cell activity was 5-15 times lower than in normal controls when measured in a 51Cr release assay and computed as lytic units 6 and 8 days respectively after virus inoculation. This difference in the levels of effector T-cell activities did not reflect slower kinetics of cytotoxic T-cell induction in antibody-treated versus control mice, since it was also obvious at 8 days after infection for Vaccinia virus and 10 and 12 days after inoculation with LCMV. CD4-specific MoAb-induced inhibition of cytotoxic T-cell responses in vivo was seen up to 150 days after treatment in thymectomized mice. However, no significant suppressive effect of the same antibody treatment on T-cell cytotoxicity could be observed in animals treated on day 3 or later after infection with Vaccinia virus. Injection of CD4-depleted mice with recombinant interleukin 2 (rIL-2) partially corrected the impaired virus-specific cytotoxic T-cell response, suggesting that IL-2 supply may be limiting in mice lacking T helper cells.

摘要

通过用CD4特异性单克隆抗体(MoAb)处理正常和胸腺切除的C57B1/6小鼠,研究了CD4 +辅助性T细胞在诱导抗病毒细胞毒性T细胞反应中的作用。在用痘苗病毒或淋巴细胞性脉络丛脑膜炎病毒(LCMV)感染的CD4特异性MoAb处理的小鼠中,在51Cr释放试验中测量并分别计算病毒接种后6天和8天的裂解单位时,细胞毒性T细胞活性比正常对照低5至15倍。效应T细胞活性水平的这种差异并不反映抗体处理小鼠与对照小鼠中细胞毒性T细胞诱导的动力学较慢,因为在痘苗病毒感染后8天以及接种LCMV后10天和12天也很明显。在胸腺切除的小鼠中,治疗后长达150天可见CD4特异性MoAb在体内诱导的细胞毒性T细胞反应抑制。然而,在用痘苗病毒感染后第3天或更晚处理的动物中,未观察到相同抗体处理对T细胞细胞毒性的显著抑制作用。给CD4耗竭的小鼠注射重组白细胞介素2(rIL-2)可部分纠正受损的病毒特异性细胞毒性T细胞反应,这表明在缺乏T辅助细胞的小鼠中IL-2供应可能受到限制。

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