Heterogeneous SARS-CoV-2 kinetics due to variable timing and intensity of immune responses.

Katherine Owens, Shadisadat Esmaeili-Wellman, Joshua T Schiffer
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Abstract

The viral kinetics of documented SARS-CoV-2 infections exhibit a high degree of inter-individual variability. We identified six distinct viral shedding patterns, which differed according to peak viral load, duration, expansion rate and clearance rate, by clustering data from 768 infections in the National Basketball Association cohort. Omicron variant infections in previously vaccinated individuals generally led to lower cumulative shedding levels of SARS-CoV-2 than other scenarios. We then developed a mechanistic mathematical model that recapitulated 1510 observed viral trajectories, including viral rebound and cases of reinfection. Lower peak viral loads were explained by a more rapid and sustained transition of susceptible cells to a refractory state during infection, as well as an earlier and more potent late, cytolytic immune response. Our results suggest that viral elimination occurs more rapidly during omicron infection, following vaccination, and following re-infection due to enhanced innate and acquired immune responses. Because viral load has been linked with COVID-19 severity and transmission risk, our model provides a framework for understanding the wide range of observed SARS-CoV-2 infection outcomes.

由于免疫反应的时间和强度可变,导致严重急性呼吸系统综合征冠状病毒2型动力学不均一。
记录在案的严重急性呼吸系统综合征冠状病毒2型感染的病毒动力学表现出高度的个体间变异性。我们通过对美国国家篮球协会队列中810例感染者的数据进行聚类,确定了六种不同的病毒脱落模式,这些模式因病毒载量峰值、持续时间、扩展率和清除率而异。先前接种疫苗的个体感染奥密克戎变异株通常导致严重急性呼吸系统综合征冠状病毒2型的累计脱落水平低于其他情况。然后,我们开发了一个机制数学模型,该模型概括了1510个观察到的病毒轨迹,包括病毒反弹和再次感染病例。病毒载量峰值较低的原因是,在感染期间,易感细胞更快速、更持久地转变为难治状态,以及更早、更有效的晚期细胞溶解性免疫反应。我们的研究结果表明,在奥密克戎感染期间、接种疫苗后以及由于先天和获得性免疫反应增强而再次感染后,病毒消除速度更快。由于病毒载量与新冠肺炎的严重程度和传播风险有关,我们的模型为了解广泛观察到的SARS-CoV-2感染结果提供了一个框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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