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Explaining rapid reinfections in multiple-wave influenza outbreaks: Tristan da Cunha 1971 epidemic as a case study

机译:解释多波流感爆发中的快速再感染:以特里斯坦·达·库尼亚(Tristan da Cunha)1971年的流行为例

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摘要

Influenza usually spreads through the human population in multiple-wave outbreaks. Successive reinfection of individuals over a short time interval has been explicitly reported during past pandemics. However, the causes of rapid reinfection and the role of reinfection in driving multiple-wave outbreaks remain poorly understood. To investigate these issues, we focus on a two-wave influenza A/H3N2 epidemic that occurred on the remote island of Tristan da Cunha in 1971. Over 59 days, 273 (96%) of 284 islanders experienced at least one attack and 92 (32%) experienced two attacks. We formulate six mathematical models invoking a variety of antigenic and immunological reinfection mechanisms. Using a maximum-likelihood analysis to confront model predictions with the reported incidence time series, we demonstrate that only two mechanisms can be retained: some hosts with either a delayed or deficient humoral immune response to the primary influenza infection were reinfected by the same strain, thus initiating the second epidemic wave. Both mechanisms are supported by previous empirical studies and may arise from a combination of genetic and ecological causes. We advocate that a better understanding and account of heterogeneity in the human immune response are essential to analysis of multiple-wave influenza outbreaks and pandemic planning.
机译:流感通常在多波暴发中在整个人群中传播。在过去的大流行中已明确报告了在短时间间隔内对个体进行连续再感染。但是,对于快速再感染的原因以及再感染在引发多波暴发中的作用仍然知之甚少。为了调查这些问题,我们集中于1971年在偏远的特里斯坦达库尼亚岛特里斯坦达库纳岛发生的两波A / H3N2流感流行。在59天中,284名岛民中的273名(96%)经历了至少一次袭击,而92名32%)经历了两次攻击。我们制定了六个数学模型,调用了多种抗原和免疫再感染机制。使用最大似然分析来对模型预测与报告的发病时间序列进行对峙,我们证明只有两种机制可以保留:某些宿主对原发性流感感染的体液免疫反应延迟或不足,但又被同一株感染,从而引发第二次流行病流行。这两种机制都得到先前经验研究的支持,可能是遗传和生态原因的结合。我们主张更好地理解和解释人类免疫应答中的异质性对于分析多波流感爆发和大流行规划至关重要。

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