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Rebound of SARS-CoV-2 Infection after Nirmatrelvir-Ritonavir Treatment.奈玛特韦-利托那韦治疗后新型冠状病毒2型感染的反弹
N Engl J Med. 2022 Sep 15;387(11):1045-1047. doi: 10.1056/NEJMc2206449. Epub 2022 Sep 7.
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J Med Virol. 2022 Nov;94(11):5543-5546. doi: 10.1002/jmv.27974. Epub 2022 Jul 11.
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Duration of Shedding of Culturable Virus in SARS-CoV-2 Omicron (BA.1) Infection.新型冠状病毒奥密克戎(BA.1)感染中可培养病毒的脱落持续时间。
N Engl J Med. 2022 Jul 21;387(3):275-277. doi: 10.1056/NEJMc2202092. Epub 2022 Jun 29.
7
Viral Dynamics of Omicron and Delta Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants With Implications for Timing of Release from Isolation: A Longitudinal Cohort Study.奥密克戎和德尔塔变异株严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的病毒动力学及其对隔离期结束时间的影响:一项纵向队列研究。
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Characterization of Virologic Rebound Following Nirmatrelvir-Ritonavir Treatment for Coronavirus Disease 2019 (COVID-19).新型冠状病毒病 2019(COVID-19)经奈玛特韦-利托那韦治疗后病毒学反弹的特征。
Clin Infect Dis. 2023 Feb 8;76(3):e526-e529. doi: 10.1093/cid/ciac512.
9
Comparison of outward transmission potential between vaccinated and partially vaccinated or unvaccinated individuals with the SARS-CoV-2 delta variant infection.接种疫苗者与部分接种疫苗或未接种疫苗的感染新冠病毒德尔塔变异株个体之间的向外传播潜力比较。
J Infect. 2022 Sep;85(3):e69-e71. doi: 10.1016/j.jinf.2022.06.002. Epub 2022 Jun 12.
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SARS-CoV-2 Omicron Variant, Lineage BA.1, Is Associated with Lower Viral Load in Nasopharyngeal Samples Compared to Delta Variant.SARS-CoV-2 奥密克戎变异株 BA.1 谱系与德尔塔变异株相比,鼻咽样本中的病毒载量较低。
Viruses. 2022 Apr 28;14(5):919. doi: 10.3390/v14050919.

德尔塔和奥密克戎变异株患者的二代发病率和活病毒脱落率比较:一项前瞻性队列研究。

Comparison of secondary attack rate and viable virus shedding between patients with SARS-CoV-2 Delta and Omicron variants: A prospective cohort study.

机构信息

Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.

Department of Biomedical Sciences, BK21 Graduate Program, Korea University College of Medicine, Seoul, Republic of Korea.

出版信息

J Med Virol. 2023 Jan;95(1):e28369. doi: 10.1002/jmv.28369.

DOI:10.1002/jmv.28369
PMID:36458559
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9877691/
Abstract

There are limited data comparing the transmission rates and kinetics of viable virus shedding of the Omicron variant to those of the Delta variant. We compared these rates in hospitalized patients infected with Delta and Omicron variants. We prospectively enrolled adult patients with COVID-19 admitted to a tertiary care hospital in South Korea between September 2021 and May 2022. Secondary attack rates were calculated by epidemiologic investigation, and daily saliva samples were collected to evaluate viral shedding kinetics. Genomic and subgenomic SARS-CoV-2 RNA was measured by PCR, and virus culture was performed from daily saliva samples. A total of 88 patients with COVID-19 who agreed to daily sampling and were interviewed, were included. Of the 88 patients, 48 (59%) were infected with Delta, and 34 (41%) with Omicron; a further 5 patients gave undetectable or inconclusive RNA PCR results and 1 was suspected of being coinfected with both variants. Omicron group had a higher secondary attack rate (31% [38/124] vs. 7% [34/456], p < 0.001). Survival analysis revealed that shorter viable virus shedding period was observed in Omicron variant compared with Delta variant (median 4, IQR [1-7], vs. 8.5 days, IQR [5-12 days], p < 0.001). Multivariable analysis revealed that moderate-to-critical disease severity (HR: 1.96), and immunocompromised status (HR: 2.17) were independent predictors of prolonged viral shedding, whereas completion of initial vaccine series or first booster-vaccinated status (HR: 0.49), and Omicron infection (HR: 0.44) were independently associated with shorter viable virus shedding. Patients with Omicron infections had higher transmission rates but shorter periods of transmissible virus shedding than those with Delta infections.

摘要

关于奥密克戎变异株活病毒脱落的传播率和动力学与德尔塔变异株相比的数据有限。我们比较了住院感染德尔塔和奥密克戎变异株的患者的这些比率。我们前瞻性地招募了 2021 年 9 月至 2022 年 5 月期间在韩国一家三级保健医院因 COVID-19 住院的成年患者。通过流行病学调查计算二次攻击率,并采集每日唾液样本评估病毒脱落动力学。通过 PCR 测量全基因组和亚基因组 SARS-CoV-2 RNA,从每日唾液样本中进行病毒培养。共纳入 88 例同意每日采样和接受访谈的 COVID-19 患者。88 例患者中,48 例(59%)感染德尔塔,34 例(41%)感染奥密克戎;另有 5 例 RNA PCR 结果不可检测或不确定,1 例疑似同时感染两种变异株。奥密克戎组的二次攻击率较高(31%[38/124] vs. 7%[34/456],p<0.001)。生存分析显示,与德尔塔变异株相比,奥密克戎变异株的活病毒脱落期更短(中位数 4 天,IQR[1-7] vs. 8.5 天,IQR[5-12 天],p<0.001)。多变量分析显示,中度至重症疾病严重程度(HR:1.96)和免疫功能低下状态(HR:2.17)是病毒脱落延长的独立预测因素,而初始疫苗系列完成或首次加强疫苗接种状态(HR:0.49)和奥密克戎感染(HR:0.44)与较短的活病毒脱落独立相关。奥密克戎感染患者的传播率较高,但具有传染性的病毒脱落期比德尔塔感染患者短。