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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:丙型肝炎病毒宿主内部适应性的计算分析和建模:HCV准种的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-immunoreactivity 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)是全球范围内肝脏疾病的主要原因。了解负责建立慢性HCV感染的机制对于开发有效的疗法和疫苗至关重要。大多数模型假设的宿主内HCV进化机制是基于通过随机突变的免疫逃逸。然而,连续的免疫逃逸并不能解释我们在慢性感染期间阴性选择持续增加的观察结果,这表明宿主体内HCV的广泛适应性。使用交叉免疫反应性模型,我们显示HCV宿主内适应水平与HCV准种之间的交叉免疫反应率相关。我们提出了一种数学模型,描述了准种之间的免疫学相互作用,除了中和作用外,还涉及非中和的交叉免疫反应性。该模型描述了HCV变体如何刺激免疫反应并持续存在,这是由于它们能够刺激较早产生的针对先前变体的非中和免疫反应,而不会引起针对变体本身的特异性反应。

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