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COVID-19 后急性后遗症(PASC)中的 SARS-CoV-2 储主。

SARS-CoV-2 reservoir in post-acute sequelae of COVID-19 (PASC).

机构信息

PolyBio Research Foundation, Medford, MA, USA.

Division of Neurotherapeutics, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Nat Immunol. 2023 Oct;24(10):1616-1627. doi: 10.1038/s41590-023-01601-2. Epub 2023 Sep 4.


DOI:10.1038/s41590-023-01601-2
PMID:37667052
Abstract

Millions of people are suffering from Long COVID or post-acute sequelae of COVID-19 (PASC). Several biological factors have emerged as potential drivers of PASC pathology. Some individuals with PASC may not fully clear the coronavirus SARS-CoV-2 after acute infection. Instead, replicating virus and/or viral RNA-potentially capable of being translated to produce viral proteins-persist in tissue as a 'reservoir'. This reservoir could modulate host immune responses or release viral proteins into the circulation. Here we review studies that have identified SARS-CoV-2 RNA/protein or immune responses indicative of a SARS-CoV-2 reservoir in PASC samples. Mechanisms by which a SARS-CoV-2 reservoir may contribute to PASC pathology, including coagulation, microbiome and neuroimmune abnormalities, are delineated. We identify research priorities to guide the further study of a SARS-CoV-2 reservoir in PASC, with the goal that clinical trials of antivirals or other therapeutics with potential to clear a SARS-CoV-2 reservoir are accelerated.

摘要

数以百万计的人患有长新冠或新冠后急性后遗症(PASC)。一些生物学因素已被认为是 PASC 病理的潜在驱动因素。一些 PASC 患者在急性感染后可能无法完全清除冠状病毒 SARS-CoV-2。相反,复制的病毒和/或病毒 RNA——可能有能力被翻译以产生病毒蛋白——作为“储库”在组织中持续存在。这个储库可以调节宿主的免疫反应,或将病毒蛋白释放到循环中。在这里,我们回顾了已识别出在 PASC 样本中存在 SARS-CoV-2 RNA/蛋白或免疫反应指示的 SARS-CoV-2 储库的研究。阐述了 SARS-CoV-2 储库可能导致 PASC 病理的机制,包括凝血、微生物组和神经免疫异常。我们确定了研究重点,以指导对 PASC 中 SARS-CoV-2 储库的进一步研究,目标是加速具有清除 SARS-CoV-2 储库潜力的抗病毒药物或其他治疗药物的临床试验。

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[4]
Association between vaccination uptake, vaccine type, and long COVID in rural Indonesia.

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[5]
Peripheral immune progression to long COVID is associated with mitochondrial gene transcription: A meta-analysis.

Mitochondrion. 2025-7-28

[6]
Effect of obesity on the acute response to SARS-CoV-2 infection and development of post-acute sequelae of COVID-19 (PASC) in nonhuman primates.

PLoS Pathog. 2025-7-24

[7]
Hamsters with long COVID present distinct transcriptomic profiles associated with neurodegenerative processes in brainstem.

Nat Commun. 2025-7-22

[8]
Deoxygenation Trends and Their Multivariate Association with Self-Reported Fatigue in Post-COVID Syndrome.

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[9]
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[10]
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本文引用的文献

[1]
Post-acute sequelae of COVID-19 is characterized by diminished peripheral CD8β7 integrin T cells and anti-SARS-CoV-2 IgA response.

Nat Commun. 2023-3-30

[2]
Clonal replacement sustains long-lived germinal centers primed by respiratory viruses.

Cell. 2023-1-5

[3]
Adaptive immune responses to SARS-CoV-2 persist in the pharyngeal lymphoid tissue of children.

Nat Immunol. 2023-1

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SARS-CoV-2 infection and persistence in the human body and brain at autopsy.

Nature. 2022-12

[5]
Lingering SARS-CoV-2 in Gastric and Gallbladder Tissues of Patients with Previous COVID-19 Infection Undergoing Bariatric Surgery.

Obes Surg. 2023-1

[6]
Distorted TCR repertoires define multisystem inflammatory syndrome in children.

PLoS One. 2022

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SARS-CoV-2 disrupts host epigenetic regulation via histone mimicry.

Nature. 2022-10

[8]
Case report: Persistence of residual antigen and RNA of the SARS-CoV-2 virus in tissues of two patients with long COVID.

Front Immunol. 2022

[9]
Evidence of SARS-CoV-2 spike protein on retrieved thrombi from COVID-19 patients.

J Hematol Oncol. 2022-8-16

[10]
Association of COVID-19 with New-Onset Alzheimer's Disease.

J Alzheimers Dis. 2022

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