人类共循环病原体:对机械传播模式的系统回顾。

IF 3.5
Proceedings. Biological sciences Pub Date : 2025-09-01 Epub Date: 2025-09-24 DOI:10.1098/rspb.2025.1453
Kelsey E Shaw, Jennifer K Peterson, Neda Jalali, Saikanth Ratnavale, Manar Alkuzweny, Carly Barbera, Alan Costello, Liam Emerick, Guido Espana, Alex Meyer, Stacy Mowry, Marya Poterek, Carol de Souza Moreira, Eric Lease Morgan, Sean Moore, Alex Perkins
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引用次数: 0

摘要

从历史上看,大多数传染病动力学的数学模型都集中在单一病原体上,尽管现实世界中共循环的病原体无处不在。我们对326篇已发表的论文进行了系统回顾,其中包括人类病原体共循环的机制、种群水平模型。我们确定了本文献中所代表的病原体类型,使用的技术和进行这些研究的动机。我们还创建了一个相互作用指数来量化共循环病原体模型包括跨规模和/或病原体-病原体相互作用的程度。我们发现,新病原体(如HIV和SARS-CoV-2)的出现,促进了新出现病原体与已建立病原体的建模活动。病原体特征也倾向于驱动建模活动;例如,HIV抑制免疫反应,当它与其他病原体一起建模时,会引起有趣的动态变化。推动这些研究的动机各不相同,但可分为两大类:探索动态和评估干预措施。我们确定的未来潜在研究途径包括调查误诊临床相似共循环病原体的影响,以及描述一种病原体对可用公共卫生资源的影响,以减少其他病原体的传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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 326 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 an interaction index to quantify the degree to which co-circulating pathogen models include across scale and/or pathogen-pathogen interactions. We found that the emergence of new pathogens, such as HIV and SARS-CoV-2, precipitated modelling activity of the emerging pathogen with established pathogens. Pathogen characteristics also tended to drive modelling activity; for example, HIV suppresses the immune response, eliciting interesting dynamics when it is modelled 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. 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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