Department of Epidemiology, University of Michigan School of Public Health, United States.
Department of Epidemiology, University of Michigan School of Public Health, United States.
Epidemics. 2017 Sep;20:21-36. doi: 10.1016/j.epidem.2017.02.013. Epub 2017 Mar 1.
Waning immunity could allow transmission of polioviruses without causing poliomyelitis by promoting silent circulation (SC). Undetected SC when oral polio vaccine (OPV) use is stopped could cause difficult to control epidemics. Little is known about waning. To develop theory about what generates SC, we modeled a range of waning patterns. We varied both OPV and wild polio virus (WPV) transmissibility, the time from beginning vaccination to reaching low polio levels, and the infection to paralysis ratio (IPR). There was longer SC when waning continued over time rather than stopping after a few years, when WPV transmissibility was higher or OPV transmissibility was lower, and when the IPR was higher. These interacted in a way that makes recent emergence of prolonged SC a possibility. As the time to reach low infection levels increased, vaccine rates needed to eliminate polio increased and a threshold was passed where prolonged low-level SC emerged. These phenomena were caused by increased contributions to the force of infection from reinfections. The resulting SC occurs at low levels that would be difficult to detect using environmental surveillance. For all waning patterns, modest levels of vaccination of adults shortened SC. Previous modeling studies may have missed these phenomena because (1) they used models with no or very short duration waning and (2) they fit models to paralytic polio case counts. Our analyses show that polio case counts cannot predict SC because nearly identical polio case count patterns can be generated by a range of waning patterns that generate different patterns of SC. We conclude that the possibility of prolonged SC is real but unquantified, that vaccinating modest fractions of adults could reduce SC risk, and that joint analysis of acute flaccid paralysis and environmental surveillance data can help assess SC risks and ensure low risks before stopping OPV.
免疫衰减可导致脊髓灰质炎病毒(PV)在不引起小儿麻痹症的情况下传播,从而促进无症状循环(SC)。停止口服脊髓灰质炎疫苗(OPV)使用后,未被发现的 SC 可能会引发难以控制的疫情。目前对免疫衰减知之甚少。为了建立有关 SC 产生原因的理论,我们对一系列衰减模式进行了建模。我们改变了 OPV 和野生脊灰病毒(WPV)的传染性、从开始接种疫苗到达到低脊灰水平的时间以及感染到瘫痪的比例(IPR)。当免疫衰减持续时间较长而不是在几年后停止时,当 WPV 传染性较高或 OPV 传染性较低时,以及当 IPR 较高时,SC 持续时间较长。这些因素相互作用,使得最近出现的长时间 SC 成为可能。随着达到低感染水平的时间增加,消除脊髓灰质炎所需的疫苗接种率增加,并且在延长的低水平 SC 出现的阈值被超过。这些现象是由再感染对感染力的贡献增加引起的。由此产生的 SC 发生在低水平,使用环境监测很难发现。对于所有衰减模式,对成年人进行适度的疫苗接种可以缩短 SC。以前的建模研究可能错过了这些现象,原因是:(1)它们使用的模型没有或衰减时间很短;(2)它们根据麻痹性脊髓灰质炎病例数拟合模型。我们的分析表明,脊髓灰质炎病例数不能预测 SC,因为几乎相同的脊髓灰质炎病例数模式可以由一系列产生不同 SC 模式的衰减模式产生。我们得出结论,长时间 SC 的可能性是真实的,但尚未量化,对成年人进行适度的疫苗接种可以降低 SC 风险,急性弛缓性麻痹和环境监测数据的联合分析可以帮助评估 SC 风险,并在停止 OPV 之前确保低风险。