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免疫功能低下人群中新冠病毒长期排毒的系统评价

A Systematic Review of Prolonged SARS-CoV-2 Shedding in Immunocompromised Persons.

作者信息

Christofferson Rebecca C, Giovanni Jennifer E, Koumans Emily H, Ategbole Muyiwa, Clark Samantha D, Godfred-Cato Shana, Menon Manoj P, Sastalla Inka, Schweitzer Beth K, Uyeki Timothy M

机构信息

Louisiana State University School of Veterinary Medicine, Baton Rouge, Louisiana, USA.

Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

出版信息

Influenza Other Respir Viruses. 2025 May;19(5):e70121. doi: 10.1111/irv.70121.


DOI:10.1111/irv.70121
PMID:40394759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12092234/
Abstract

BACKGROUND: Although reports have documented prolonged SARS-CoV-2 RNA detection in immunocompromised patients, few studies have systematically analyzed data on duration of SARS-CoV-2 in respiratory specimens of immunocompromised patients. METHODS: A systematic review was undertaken to describe SARS-CoV-2 RNA and infectious virus detection in immunocompromised patients from published data between January 1, 2020 and July 1, 2022. Patients were included if there was ≥ 1 positive SARS-CoV-2 RNA result in respiratory specimens collected > 20 days since symptom onset or first positive SARS-CoV-2 RT-PCR result. RESULTS: Of the 183 patients, 175 were symptomatic with 83 (47.4%) that experienced intermittent relapsing symptoms, while pneumonia was reported in 122 (66.7%). Immunocompromising conditions represented were hematologic malignancy treatment (89, 48.6%), solid organ transplant (47, 25.7%), autoimmune disease treatment (14, 7.7%), solid tumor treatment (3, 1.6%), HIV infection (15, 8.2%), and primary immunodeficiency (15, 8.2%). Median duration from the first to the last positive SARS-CoV-2 RT-PCR result was 56 days in upper respiratory and 60 days in lower respiratory tract specimens. Significant differences in median duration of SARS-CoV-2 RNA detection were observed between patients with and without pneumonia and for patients with hematologic malignancies compared to solid organ transplant patients. Among patients with viral culture performed, median duration of replication-competent SARS-CoV-2 was 60.5 days from symptom onset (maximum 238 days) and 59 days from first RT-PCR positive result (maximum 268 days). CONCLUSIONS: Immunocompromised persons can have replication-competent SARS-CoV-2 in respiratory tissues for months, including while asymptomatic. Serial SARS-CoV-2 testing can inform the duration of isolation for immunocompromised patients with SARS-CoV-2 infection.

摘要

背景:尽管有报告记录了免疫功能低下患者中SARS-CoV-2 RNA检测时间延长的情况,但很少有研究系统分析免疫功能低下患者呼吸道标本中SARS-CoV-2持续时间的数据。 方法:进行了一项系统综述,以根据2020年1月1日至2022年7月1日期间发表的数据描述免疫功能低下患者中SARS-CoV-2 RNA和传染性病毒的检测情况。如果自症状出现或首次SARS-CoV-2 RT-PCR检测结果呈阳性起20天以上采集的呼吸道标本中SARS-CoV-2 RNA检测结果≥1次为阳性,则纳入患者。 结果:在183例患者中,175例有症状,其中83例(47.4%)经历间歇性复发症状,122例(66.7%)报告有肺炎。所代表的免疫功能低下情况包括血液系统恶性肿瘤治疗(89例,48.6%)、实体器官移植(47例,25.7%)、自身免疫性疾病治疗(14例,7.7%)、实体瘤治疗(3例,1.6%)、HIV感染(15例,8.2%)和原发性免疫缺陷(15例,8.2%)。上呼吸道标本中从首次到最后一次SARS-CoV-2 RT-PCR检测结果呈阳性的中位持续时间为56天,下呼吸道标本为60天。在有肺炎和无肺炎的患者之间以及血液系统恶性肿瘤患者与实体器官移植患者之间,观察到SARS-CoV-2 RNA检测中位持续时间存在显著差异。在进行病毒培养的患者中,有复制能力的SARS-CoV-2从症状出现开始的中位持续时间为60.5天(最长238天),从首次RT-PCR检测结果呈阳性开始为59天(最长268天)。 结论:免疫功能低下者呼吸道组织中可有数月存在有复制能力的SARS-CoV-2,包括无症状时。连续进行SARS-CoV-2检测可为感染SARS-CoV-2的免疫功能低下患者的隔离持续时间提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/12092234/204113d7b009/IRV-19-e70121-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/12092234/3069aef7034a/IRV-19-e70121-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/12092234/0b9e686a7c4b/IRV-19-e70121-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/12092234/204113d7b009/IRV-19-e70121-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/12092234/3069aef7034a/IRV-19-e70121-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/12092234/0b9e686a7c4b/IRV-19-e70121-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a4/12092234/204113d7b009/IRV-19-e70121-g002.jpg

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引用本文的文献

[1]
Correction to "A Systematic Review of Prolonged SARS-CoV-2 Shedding in Immunocompromised Persons".

Influenza Other Respir Viruses. 2025-6

本文引用的文献

[1]
The revised JBI critical appraisal tool for the assessment of risk of bias for cohort studies.

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[2]
Relapse of COVID-19 and Viral Evolution in a Patient With Good Syndrome: A Case Report.

Cureus. 2024-1-19

[3]
SARS-CoV-2 shedding and evolution in patients who were immunocompromised during the omicron period: a multicentre, prospective analysis.

Lancet Microbe. 2024-3

[4]
SARS-CoV-2 viral clearance and evolution varies by type and severity of immunodeficiency.

Sci Transl Med. 2024-1-24

[5]
The Association Between Antibody Responses and Prolonged Viable Severe Acute Respiratory Syndrome Coronavirus 2 Shedding in Immunocompromised Patients: A Prospective Cohort Study.

J Infect Dis. 2024-6-14

[6]
Virological characteristics and the rapid antigen test as deisolation criteria in immunocompromised patients with COVID-19: A prospective cohort study.

J Med Virol. 2023-11

[7]
Duration of viable virus shedding and polymerase chain reaction positivity of the SARS-CoV-2 Omicron variant in the upper respiratory tract: a systematic review and meta-analysis.

Int J Infect Dis. 2023-4

[8]
Characteristics and risk factors of prolonged viable virus shedding in immunocompromised patients with COVID-19: a prospective cohort study.

J Infect. 2023-4

[9]
Long-term SARS-CoV-2 Asymptomatic Carriage in an Immunocompromised Host: Clinical, Immunological, and Virological Implications.

J Clin Immunol. 2022-10

[10]
Detectable Duration of Viable SARS-CoV-2, Total and Subgenomic SARS-CoV-2 RNA in Noncritically Ill COVID-19 Patients: a Prospective Cohort Study.

Microbiol Spectr. 2022-6-29

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