Co-circulating pathogens of humans: A systematic review of mechanistic transmission models

Kelsey Shaw, Jennifer Peterson, Neda Jalali, Saikanth Ratnavale, Manar Alkuzweny, Carly Barbera, Alan Costello, Liam Emerick, Guido Espana, Alexander Meyer, Stacy Mowry, Marya Poterek, Carol de Souza Moreira, Eric Morgan, Sean M Moore, Alex Perkins
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Abstract

Historically, most mathematical models of infectious disease dynamics have focused on a single pathogen, despite the ubiquity of co-circulating pathogens in the real world. We conducted a systematic review of 311 published papers that included a mechanistic, population-level model of co-circulating human pathogens. We identified the types of pathogens represented in this literature, techniques used, and motivations for conducting these studies. We also created a complexity index to quantify the degree to which co-circulating pathogen models diverged from single-pathogen models. We found that the emergence of new pathogens, such as HIV and SARS-CoV-2, precipitated modeling activity of the emerging pathogen with established pathogens. Pathogen characteristics also tended to drive modeling activity; for example, HIV suppresses the immune response, eliciting interesting dynamics when it is modeled with other pathogens. The motivations driving these studies were varied but could be divided into two major categories: exploration of dynamics and evaluation of interventions. Finally, we found that model complexity quickly increases as additional pathogens are added. Future potential avenues of research we identified include investigating the effects of misdiagnosis of clinically similar co-circulating pathogens and characterizing the impacts of one pathogen on public health resources available to curtail the spread of other pathogens.
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人类共循环病原体:机理传播模型的系统回顾
从历史上看,大多数传染病动态数学模型都只关注单一病原体,尽管在现实世界中共同流行的病原体无处不在。我们对已发表的 311 篇论文进行了系统性综述,这些论文包含了人类病原体共循环的机理、种群水平模型。我们确定了这些文献中的病原体类型、使用的技术以及开展这些研究的动机。我们还创建了一个复杂性指数,以量化共循环病原体模型与单一病原体模型的差异程度。我们发现,HIV 和 SARS-CoV-2 等新病原体的出现促进了新病原体与既有病原体的建模活动。病原体的特征也往往会推动建模活动;例如,艾滋病病毒会抑制免疫反应,当它与其他病原体一起建模时,就会产生有趣的动态变化。推动这些研究的动机多种多样,但可分为两大类:探索动力学和评估干预措施。最后,我们发现,随着病原体的增加,模型的复杂性也会迅速增加。我们确定的未来潜在研究方向包括调查临床上类似的共同传播病原体的误诊影响,以及描述一种病原体对可用于遏制其他病原体传播的公共卫生资源的影响。
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