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病毒特异性细胞毒性T细胞在小鼠中引发的病毒触发免疫抑制。

Virus-triggered immune suppression in mice caused by virus-specific cytotoxic T cells.

作者信息

Leist T P, Rüedi E, Zinkernagel R M

机构信息

Institut für Pathologie, Universitätsspital, Zürich, Switzerland.

出版信息

J Exp Med. 1988 May 1;167(5):1749-54. doi: 10.1084/jem.167.5.1749.

Abstract

Normal mice infected with 10(5) infectious doses of lymphocytic choriomeningitis virus (LCMV, WE isolate) generated a reduced or no T cell-independent IgM and/or T cell-dependent IgG response to a subsequent vesicular stomatitis virus Indiana (VSV-IND) injection; this transient immune suppression lasted for weeks to months. Connatally infected LCMV-carrier mice or acutely infected T cell-deficient nude mice had normal anti-VSV IgM and IgG or IgM responses respectively. LCMV-infected nude mice transfused with helper cell-depleted LCMV-specific immune spleen cells were immunosuppressed. Normal mice infected with LCMV but treated with a rat anti-CD8 mAb (that had been shown previously to eliminate cytotoxic T cells in vivo) and then infected with VSV exhibited a normal anti-VSV IgM and IgG response. Since no IFN-alpha or -beta was detected on, or after, day 6 of LCMV infection, neither LCMV alone, nor IFN induced by it caused the observed immune suppression; the presented evidence suggests that LCMV-immune CD8+ T cells were responsible for it. It is conceivable that a similar pathogenesis where virus-specific cytotoxic T cells may destroy virus-infected cells essentially involved in an immune response (APC, T helper cells, etc.) may be involved in other virally triggered immune suppression or in AIDS.

摘要

用10⁵个感染剂量的淋巴细胞性脉络丛脑膜炎病毒(LCMV,WE株)感染正常小鼠后,对随后注射的水疱性口炎病毒印第安纳株(VSV-IND)产生的非T细胞依赖性IgM和/或T细胞依赖性IgG反应减弱或无反应;这种短暂的免疫抑制持续数周或数月。先天性感染LCMV的携带小鼠或急性感染的T细胞缺陷裸鼠分别具有正常的抗VSV IgM和IgG或IgM反应。用去除辅助细胞的LCMV特异性免疫脾细胞输注的LCMV感染裸鼠受到免疫抑制。用大鼠抗CD8单克隆抗体(先前已证明可在体内消除细胞毒性T细胞)处理后感染LCMV,然后再感染VSV的正常小鼠表现出正常的抗VSV IgM和IgG反应。由于在LCMV感染后第6天及之后均未检测到IFN-α或-β,因此单独的LCMV及其诱导的IFN均未导致观察到的免疫抑制;现有证据表明LCMV免疫的CD8⁺T细胞对此负责。可以想象,在其他病毒引发的免疫抑制或艾滋病中,可能涉及类似的发病机制,即病毒特异性细胞毒性T细胞可能破坏基本参与免疫反应的病毒感染细胞(APC、T辅助细胞等)。

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