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Computational analysis and modelling of intra-host adaptation of hepatitis C virus: the role of immune cross-reactivity of HCV quasispecies

机译:丙型肝炎病毒中宿主内适应的计算分析与建模:HCV Quaspecies免疫交叉反应性的作用

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Hepatitis C virus (HCV) is a major cause of liver disease worldwide. Understanding the mechanisms responsible for the establishment of chronic HCV infection is critical to the development of efficient therapeutics and vaccines. The mechanism of intra-host HCV evolution assumed by most models is based on immune escape via random mutations. However, continuous immune escape does not explain our observation of a consistent increase in negative selection during chronic infection, which suggests extensive intra-host HCV adaptation. Using a model of cross-immunoreactivity, we show that the level of HCV intra-host adaptation correlates with the rate of cross-immunoreacivity among HCV quasispecies. We present a mathematical model describing the immunological interaction among quasispecies that involves, in addition to neutralization, a non-neutralizing cross-immunoreactivity. The model describes how HCV variants escape immune responses and persist, owing to their capability to stimulate non-neutralizing immune responses developed earlier against preceding variants without eliciting specific responses against the variant itself.
机译:丙型肝炎病毒(HCV)是全世界肝病的主要原因。了解负责建立慢性HCV感染的机制对于开发有效的治疗和疫苗至关重要。大多数模型假设的宿主HCV演化的机制基于免疫突变的免疫逃逸。然而,连续免疫逃逸并未解释我们观察慢性感染期间阴性选择的一致增加,这表明宿主内的HCV适应。使用交叉免疫反应性的模型,我们表明HCV内宿主的水平与HCV Quaspecies之间的交叉免疫率的速率相关。我们介绍了一种描述涉及的Quasispecies之间的免疫相互作用的数学模型,除了中和,还具有非中和交叉免疫反应性。该模型描述了HCV变体如何逃避免疫应答并持续存在,这是由于它们刺激前面患者的不中和免疫应答的能力,而不会引发针对变形本身的特定反应。

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