• Bmc Infect Dis · Nov 2020

    Observational Study

    Kinetic changes in virology, specific antibody response and imaging during the clinical course of COVID-19: a descriptive study.

    • Qiu-Jing Wang, Yan-Zhen Yao, Jun-Shuai Song, Qiao Wang, Li-Yun Xu, Zhou-Jun Bao, Dai-Wen Mao, Ji-Hang Zhou, Zhe-En Zhang, Yan Wang, Yi-Wei Li, He-Ping Wang, Lue Li, Hai-Yan Pan, Guo-Qiang Zhang, and Shi-Bo Li.
    • Department of Infectious Diseases, Zhoushan Hospital, Wenzhou Medical University, NO.739 Dingshen Road, Zhoushan City, 316021, Zhejiang, China.
    • Bmc Infect Dis. 2020 Nov 10; 20 (1): 818.

    BackgroundTo explore the kinetic changes in virology, specific antibody response and imaging during the clinical course of COVID-19.MethodsThis observational study enrolled 20 patients with COVID-19, who were hospitalized between January 20-April 6, 2020, in the two COVID-19 designated hospitals of Zhoushan, Zhejiang and Rushan, Shandong, China, The laboratory findings, imaging, serum response to viral infection, and viral RNA level in the throat and stool samples were assessed from onset to recovery phase in patients with COVID-19.ResultsSARS-COV-2 RNA was positive as early as day four. It remained positive until day 55 post-onset in the sputum-throat swabs and became negative in most cases (55%) within 14 days after onset. Lymphocytopenia occurred in 40% (8/20) of patients during the peak infection period and returned to normal at week five. The most severe inflammation in the lungs appeared in week 2 or 3 after onset, and this was completely absorbed between week 6 and 8 in 85.7% of patients. All patients had detectable antibodies to the receptor binding domain (RBD), and 95% of these patients had IgG to viral N proteins. The antibody titer peaked at week four. Anti-S IgM was positive in 7 of 20 patients after week three.ConclusionsAll COVID-19 patients in this study were self-limiting and recovered well though it may take as long as 6-8 weeks. Our findings on the kinetic changes in imaging, serum response to viral infection and viral RNA level may help understand pathogenesis and define clinical course of COVID-19.

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