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了解 COVID-19 的结果——当前的急性呼吸道感染模型真的适用吗?

Understanding the outcomes of COVID-19 - does the current model of an acute respiratory infection really fit?

机构信息

Nuffield Department of Medicine, University of Oxford, Oxford, UK.

National Microbiology Services, NHS Blood and Transplant, London, UK.

出版信息

J Gen Virol. 2021 Mar;102(3). doi: 10.1099/jgv.0.001545. Epub 2020 Dec 15.

Abstract

Although coronavirus disease 2019 (COVID-19) is regarded as an acute, resolving infection followed by the development of protective immunity, recent systematic literature review documents evidence for often highly prolonged shedding of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in respiratory and faecal samples, periodic recurrence of PCR positivity in a substantial proportion of individuals and increasingly documented instances of reinfection associated with a lack of protective immunity. This pattern of infection is quite distinct from the acute/resolving nature of other human pathogenic respiratory viruses, such as influenza A virus and respiratory syncytial virus. Prolonged shedding of SARS-CoV-2 furthermore occurs irrespective of disease severity or development of virus-neutralizing antibodies. SARS-CoV-2 possesses an intensely structured RNA genome, an attribute shared with other human and veterinary coronaviruses and with other mammalian RNA viruses such as hepatitis C virus. These are capable of long-term persistence, possibly through poorly understood RNA structure-mediated effects on innate and adaptive host immune responses. The assumption that resolution of COVID-19 and the appearance of anti-SARS-CoV-2 IgG antibodies represents virus clearance and protection from reinfection, implicit for example in the susceptible-infected-recovered (SIR) model used for epidemic prediction, should be rigorously re-evaluated.

摘要

尽管 2019 年冠状病毒病(COVID-19)被认为是一种急性、可自行缓解的感染,随后产生保护性免疫,但最近的系统文献回顾记录了严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)在呼吸道和粪便样本中经常高度延长排出、相当一部分个体中 PCR 阳性周期性复发以及越来越多的与缺乏保护性免疫相关的再感染实例的证据。这种感染模式与其他人类致病呼吸道病毒(如甲型流感病毒和呼吸道合胞病毒)的急性/自限性性质截然不同。SARS-CoV-2 的延长排出与疾病严重程度或病毒中和抗体的产生无关。SARS-CoV-2 具有强烈结构化的 RNA 基因组,这一属性与其他人类和兽医冠状病毒以及丙型肝炎病毒等其他哺乳动物 RNA 病毒共享。这些病毒可能通过对先天和适应性宿主免疫反应的 RNA 结构介导作用而长期存在,这一点可能尚未被充分了解。假设 COVID-19 的缓解和抗 SARS-CoV-2 IgG 抗体的出现代表病毒清除和免受再感染,例如在用于流行预测的易感-感染-恢复(SIR)模型中隐含的假设,应进行严格重新评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01ba/8222868/11be007aa5d1/jgv-102-1545-g001.jpg

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