Gunawardana Manjula, Webster Simon, Rivera Sofia, Cortez John M, Breslin Jessica, Pinales Cristian, Buser Christopher, Ibarrondo F Javier, Yang Otto O, Bobardt Michael, Gallay Philippe A, Adler Amy P, Ramirez Christina M, Anton Peter A, Baum Marc M
Department of Chemistry, Oak Crest Institute of Science, 128-132W. Chestnut Ave., Monrovia, CA USA.
University of California, Los Angeles (UCLA), Division of Infectious Diseases, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA USA.
Commun Med (Lond). 2022 Oct 11;2:129. doi: 10.1038/s43856-022-00195-4. eCollection 2022.
A comprehensive understanding of the SARS-CoV-2 infection dynamics and the ensuing host immune responses is needed to explain the pathogenesis as it relates to viral transmission. Knowledge gaps exist surrounding SARS-CoV-2 in vivo kinetics, particularly in the earliest stages after exposure.
An ongoing, workplace clinical surveillance study was used to intensely sample a small cohort longitudinally. Nine study participants who developed COVID-19 between November, 2020 and March, 2021 were monitored at high temporal resolution for three months in terms of viral loads as well as associated inflammatory biomarker and antibody responses. CD8 + T cells targeting SARS-CoV-2 in blood samples from study participants were evaluated.
Here we show that the resulting datasets, supported by Bayesian modeling, allowed the underlying kinetic processes to be described, yielding a number of unexpected findings. Early viral replication is rapid (median doubling time, 3.1 h), providing a narrow window between exposure and viral shedding, while the clearance phase is slow and heterogeneous. Host immune responses different widely across participants.
Results from our small study give a rare insight into the life-cycle of COVID-19 infection and hold a number of important biological, clinical, and public health implications.
为了解与病毒传播相关的发病机制,需要全面了解严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的感染动态及随之产生的宿主免疫反应。关于SARS-CoV-2的体内动力学,尤其是暴露后最早阶段,仍存在知识空白。
一项正在进行的职场临床监测研究对一小群人进行纵向密集采样。对2020年11月至2021年3月期间感染新型冠状病毒肺炎(COVID-19)的9名研究参与者,在三个月内以高时间分辨率监测其病毒载量以及相关炎症生物标志物和抗体反应。对研究参与者血样中靶向SARS-CoV-2的CD8 + T细胞进行了评估。
我们发现,在贝叶斯模型的支持下,所得数据集能够描述潜在的动力学过程,从而产生了一些意外发现。早期病毒复制迅速(中位加倍时间为3.1小时),在暴露和病毒脱落之间提供了一个狭窄的窗口期,而清除阶段缓慢且具有异质性。不同参与者的宿主免疫反应差异很大。
我们这项小型研究的结果为深入了解COVID-19感染的生命周期提供了难得的见解,并具有许多重要的生物学、临床和公共卫生意义。