首页> 美国卫生研究院文献>Journal of Virology >CD40 Ligand-Mediated Interactions Are Involved in the Generation of Memory CD8+ Cytotoxic T Lymphocytes (CTL) but Are Not Required for the Maintenance of CTL Memory following Virus Infection
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CD40 Ligand-Mediated Interactions Are Involved in the Generation of Memory CD8+ Cytotoxic T Lymphocytes (CTL) but Are Not Required for the Maintenance of CTL Memory following Virus Infection

机译:CD40配体介导的相互作用涉及记忆CD8 +细胞毒性T淋巴细胞(CTL)的产生但对于病毒感染后维持CTL记忆不是必需的

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摘要

CD8+ cytotoxic T lymphocytes (CTL) play a key role in the control of many virus infections, and the need for vaccines to elicit strong CD8+ T-cell responses in order to provide optimal protection in such infections is increasingly apparent. However, the mechanisms involved in the induction and maintenance of CD8+ CTL memory are currently poorly understood. In this study, we investigated the involvement of CD40 ligand (CD40L)-mediated interactions in these processes by analyzing the memory CTL response of CD40L-deficient mice following infection with lymphocytic choriomeningitis virus (LCMV). The maintenance of memory CD8+ CTL precursors (CTLp) at stable frequencies over time was not impaired in CD40L-deficient mice. By contrast, the initial generation of memory CTLp was affected. CD40L-deficient mice produced lower levels of CD8+ CTLp during the primary immune response to LCMV than did wild-type controls, despite the fact that the LCMV-specific effector CTL response of CD40L-deficient mice was indistinguishable from that of control animals. The differentiation of naïve CD8+ T cells into effector and memory CTL thus involves pathways that can be discriminated from each other by their requirement for CD40L-mediated interactions. Expression of CD40L by CTLp themselves was not an essential step during their expansion and differentiation from naïve CD8+ cells into memory CTLp; instead, the reduction in memory CTLp generation in CD40L-deficient mice was likely a consequence of defects in the CD4+ T-cell response mounted by these animals. These results thus suggest a previously unappreciated role for CD40L in the generation of CD8+ memory CTLp, the probable nature of which is discussed.
机译:CD8 + 细胞毒性T淋巴细胞(CTL)在许多病毒感染的控制中起着关键作用,并且需要疫苗以引起强烈的CD8 + T细胞应答在这种感染中提供最佳保护越来越明显。但是,目前尚不清楚CD8 + CTL记忆的诱导和维持机制。在这项研究中,我们通过分析CD40L缺陷型小鼠感染淋巴细胞性脉络膜脑膜炎病毒(LCMV)后的记忆CTL反应,研究了这些过程中CD40配体(CD40L)介导的相互作用的参与。在缺乏CD40L的小鼠中,记忆CD8 + CTL前体(CTLp)随时间保持稳定的频率不会受到损害。相比之下,内存CTLp的初始生成受到了影响。尽管缺乏CD40L缺陷小鼠的LCMV特异性效应子CTL反应是无法区分的,但CD40L缺陷小鼠在对LCMV的初次免疫应答中产生的CD8 + CTLp水平低于野生型对照。与对照动物相比因此,将原始CD8 + T细胞分化为效应CTL和记忆CTL涉及一些途径,这些途径可以通过其对CD40L介导的相互作用的需求加以区分。 CTLp自身表达CD40L并不是将其从原始CD8 + 细胞扩增和分化为记忆CTLp的必要步骤。相反,缺乏CD40L的小鼠记忆CTLp产生的减少可能是这些动物体内CD4 + T细胞应答缺陷的结果。因此,这些结果表明,CD40L在CD8 + 记忆CTLp的产生中起着前所未有的作用,并讨论了其可能的性质。

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