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Prolonged persistence of measles virus RNA is characteristic of primary infection dynamics

机译:麻疹病毒RNA的持续存在是主要感染动态的特征

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摘要

Measles virus (MeV) is the poster child for acute infection followed by lifelong immunity. However, recent work shows the presence of MeV RNA in multiple sites for up to 3 mo after infection in a proportion of infected children. Here, we use experimental infection of rhesus macaques to show that prolonged RNA presence is characteristic of primary infection. We found that viral RNA persisted in the blood, respiratory tract, or lymph nodes four to five times longer than the infectious virus and that the clearance of MeV RNA from blood happened in three phases: rapid decline coincident with clearance of infectious virus, a rebound phase with increases up to 10-fold, and a phase of slow decrease to undetect-able levels. To examine the effect of individual host immune factors on MeV load dynamics further, we developed a mathematical model that expressed viral replication and elimination in terms of the strength of MeV-specif ic T-cell responses, antibody responses, target cell limitations, and immunosuppressive activity of regulatory T cells. Based on the model, we demonstrate that viral dynamics, although initially regulated by T cells, require antibody to eliminate viral RNA. These results have profound consequences for our view of acute viral infections, the development of prolonged immunity, and, potentially, viral evolution.
机译:麻疹病毒(MeV)是急性感染的代表,其后是终生免疫。然而,最近的研究表明,在感染后的一部分儿童中,感染后长达3个月的多个位点都存在MeV RNA。在这里,我们使用恒河猴的实验性感染来证明长时间存在的RNA是原发感染的特征。我们发现病毒RNA持续存在于血液,呼吸道或淋巴结中的时间是感染性病毒的四到五倍,并且MeV RNA从血液中的清除分为三个阶段:快速下降与感染性病毒的清除同时发生,反弹阶段增加到10倍,阶段缓慢减少到无法检测的水平。为了进一步检查各个宿主免疫因子对MeV负荷动态的影响,我们开发了一个数学模型,该模型根据MeV特异性T细胞应答,抗体应答,靶细胞限制和免疫抑制的强度表达病毒复制和消除调节性T细胞的活性。基于该模型,我们证明病毒动力学虽然最初受T细胞调节,但仍需要抗体来消除病毒RNA。这些结果对我们对急性病毒感染,延长的免疫力以及潜在的病毒进化的观点具有深远的影响。

著录项

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  • 作者单位

    W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205;

    Department of Ecology and Evolutionary Biology, Woodrow Wilson School of Public and International Affairs, Princeton University, Princeton, NJ 08544;

    Department of Molecular and Comparative Pathobiology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205;

    Department of Ecology and Evolutionary Biology, Woodrow Wilson School of Public and International Affairs, Princeton University, Princeton, NJ 08544,Fogarty International Center, National Institutes of Health, Bethesda, MD 20892;

    W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    immune responses; within-host modeling; virus clearance;

    机译:免疫反应;主机内部建模;病毒清除;
  • 入库时间 2022-08-18 00:40:29

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