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与 COVID-19 临床结果相关的病毒和宿主因素。

Viral and host factors related to the clinical outcome of COVID-19.

机构信息

Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.

National Research Center for Translational Medicine, Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, Ruijin Hospital Affiliated to Shanghai Jiao Tong University (SJTU) School of Medicine, Shanghai, China.

出版信息

Nature. 2020 Jul;583(7816):437-440. doi: 10.1038/s41586-020-2355-0. Epub 2020 May 20.

DOI:10.1038/s41586-020-2355-0
PMID:32434211
Abstract

In December 2019, coronavirus disease 2019 (COVID-19), which is caused by the new coronavirus severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was identified in Wuhan (Hubei province, China); it soon spread across the world. In this ongoing pandemic, public health concerns and the urgent need for effective therapeutic measures require a deep understanding of the epidemiology, transmissibility and pathogenesis of COVID-19. Here we analysed clinical, molecular and immunological data from 326 patients with confirmed SARS-CoV-2 infection in Shanghai. The genomic sequences of SARS-CoV-2, assembled from 112 high-quality samples together with sequences in the Global Initiative on Sharing All Influenza Data (GISAID) dataset, showed a stable evolution and suggested that there were two major lineages with differential exposure history during the early phase of the outbreak in Wuhan. Nevertheless, they exhibited similar virulence and clinical outcomes. Lymphocytopenia, especially reduced CD4 and CD8 T cell counts upon hospital admission, was predictive of disease progression. High levels of interleukin (IL)-6 and IL-8 during treatment were observed in patients with severe or critical disease and correlated with decreased lymphocyte count. The determinants of disease severity seemed to stem mostly from host factors such as age and lymphocytopenia (and its associated cytokine storm), whereas viral genetic variation did not significantly affect outcomes.

摘要

2019 年 12 月,由新型冠状病毒 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) 引起的 2019 年冠状病毒病(COVID-19)在武汉(中国湖北省)被发现;它很快在全世界蔓延。在这场持续的大流行中,公众健康问题和对有效治疗措施的迫切需要要求我们深入了解 COVID-19 的流行病学、传染性和发病机制。在这里,我们分析了来自上海 326 例确诊 SARS-CoV-2 感染患者的临床、分子和免疫学数据。从 112 个高质量样本中组装的 SARS-CoV-2 基因组序列,以及 GISAID 数据集(Global Initiative on Sharing All Influenza Data)中的序列,显示出稳定的进化,并表明在武汉疫情早期有两个主要的谱系,具有不同的暴露史。然而,它们表现出相似的毒力和临床结局。淋巴细胞减少症,特别是入院时 CD4 和 CD8 T 细胞计数减少,是疾病进展的预测指标。在治疗过程中观察到高水平的白细胞介素(IL)-6 和 IL-8,在重症或危重症患者中观察到高水平的白细胞介素(IL)-6 和 IL-8,与淋巴细胞计数减少相关。疾病严重程度的决定因素似乎主要来自宿主因素,如年龄和淋巴细胞减少症(及其相关的细胞因子风暴),而病毒遗传变异并没有显著影响结局。

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Nat Med. 2020 Apr;26(4):450-452. doi: 10.1038/s41591-020-0820-9.
2
Pulmonary Pathology of Early-Phase 2019 Novel Coronavirus (COVID-19) Pneumonia in Two Patients With Lung Cancer.两例肺癌患者 2019 年新型冠状病毒(COVID-19)肺炎早期阶段的肺部病理学表现。
J Thorac Oncol. 2020 May;15(5):700-704. doi: 10.1016/j.jtho.2020.02.010. Epub 2020 Feb 28.
3
Clinical Characteristics of Coronavirus Disease 2019 in China.《中国 2019 年冠状病毒病临床特征》
Mol Biol Evol. 2025 Jun 4;42(6). doi: 10.1093/molbev/msaf118.
4
Minimalistic Transcriptomic Signatures Permit Accurate Early Prediction of COVID-19 Mortality.简约转录组特征可实现对 COVID-19 死亡率的准确早期预测。
medRxiv. 2025 May 19:2025.05.18.25327658. doi: 10.1101/2025.05.18.25327658.
5
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Physiol Rep. 2025 May;13(10):e70372. doi: 10.14814/phy2.70372.
6
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BMJ Public Health. 2025 Feb 26;3(1):e001501. doi: 10.1136/bmjph-2024-001501. eCollection 2025 Jan.
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BMC Infect Dis. 2025 Feb 25;25(1):275. doi: 10.1186/s12879-025-10643-w.
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9
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N Engl J Med. 2020 Feb 20;382(8):727-733. doi: 10.1056/NEJMoa2001017. Epub 2020 Jan 24.
10
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