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严重急性呼吸综合征冠状病毒2核蛋白与抗刺突血清学:对冠状病毒病2019疾病严重程度和死亡率的见解——ACTIV-1试验的二次分析

SARS-CoV-2 N protein and anti-spike serologies: insights into COVID-19 disease severity and mortality-a secondary analysis of the ACTIV-1 trial.

作者信息

Mena Lora Alfredo J, Enders Kimi, Wu Huimin, Parra-Rodriguez Luis, Palma Christopher, Saliba Katy, Laverdurre Sylvain, Smith P Brian, Anstrom Kevin J, Bozzette Samuel A, Powderly William G

机构信息

Division of Infectious Diseases, University of Illinois at Chicago, 808 S Wood St, RM 888, Chicago, IL 60612, USA.

University of North Carolina, Chapel Hill, NC, USA.

出版信息

Ther Adv Infect Dis. 2025 Apr 22;12:20499361251333617. doi: 10.1177/20499361251333617. eCollection 2025 Jan-Dec.

Abstract

BACKGROUND

Understanding factors that predict progression to severe COVID-19 is critical. Antibodies targeting SARS-CoV-2 spike protein confer protection, while the N protein of SARS-CoV-2 plays roles in viral replication and immune dysfunction. This study explores the significance of N protein and anti-spike antibodies on disease severity, progression, and mortality.

OBJECTIVES

To evaluate the relationship between SARS-CoV-2 N protein and anti-spike antibody levels with disease severity, clinical outcomes, and mortality in hospitalized patients with COVID-19.

DESIGN

A secondary analysis of serologic data from participants in the ACTIV-1 randomized clinical trial, which evaluated immunomodulators for the treatment of hospitalized patients with COVID-19.

METHODS

A subanalysis of the ACTIV-1 immune modulator trial was conducted. Samples collected at randomization were tested for N protein levels and anti-spike antibodies. Logistic regression and linear models were employed to examine the association between serological measures and clinical outcomes, including 28-day mortality as well as progression to high-flow nasal cannula (HFNC) and invasive mechanical ventilation (MV).

RESULTS

Among the 496 participants with detectable serum N protein, the median was 1143 ng/dL, and levels decreased from 2559 ng/dL in participants randomized at 6 days of symptom onset to 477.6 ng/dL at 11 days. Higher anti-spike antibody levels were seen as the days from symptom onset progressed or disease severity increased. Greater disease severity at randomization was associated with 28-day mortality, prolonged days of oxygenation, ventilation, hospitalization, and risk of new non-invasive ventilation, HFNC, MV, or extracorporeal membrane oxygenation use. N protein levels were associated with a higher risk of new non-invasive ventilation or HFNC use, longer oxygenation duration, and extended hospitalization. Anti-spike antibody serologies were not associated with clinical outcomes.

CONCLUSION

N protein levels could provide insights into COVID-19 disease progression and prognosis. Further research is needed to explore the clinical implications of these findings to optimize patient care and enhance outcomes.

摘要

背景

了解预测COVID-19进展为重症的因素至关重要。靶向严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白的抗体可提供保护,而SARS-CoV-2的核衣壳蛋白(N蛋白)在病毒复制和免疫功能障碍中起作用。本研究探讨N蛋白和抗刺突抗体对疾病严重程度、进展和死亡率的意义。

目的

评估SARS-CoV-2 N蛋白和抗刺突抗体水平与COVID-19住院患者的疾病严重程度、临床结局和死亡率之间的关系。

设计

对ACTIV-1随机临床试验参与者的血清学数据进行二次分析,该试验评估了免疫调节剂用于治疗COVID-19住院患者的疗效。

方法

对ACTIV-1免疫调节剂试验进行亚分析。在随机分组时采集的样本检测N蛋白水平和抗刺突抗体。采用逻辑回归和线性模型来检验血清学指标与临床结局之间的关联,包括28天死亡率以及进展为高流量鼻导管吸氧(HFNC)和有创机械通气(MV)的情况。

结果

在496名可检测到血清N蛋白的参与者中,中位数为1143 ng/dL,水平从症状出现6天时随机分组的参与者的2559 ng/dL降至11天时的477.6 ng/dL。随着症状出现天数的增加或疾病严重程度的加重,抗刺突抗体水平升高。随机分组时疾病严重程度越高,与28天死亡率、延长的氧疗天数、通气天数、住院天数以及使用新的无创通气、HFNC、MV或体外膜肺氧合的风险相关。N蛋白水平与使用新的无创通气或HFNC的较高风险、更长的氧疗持续时间和更长的住院时间相关。抗刺突抗体血清学与临床结局无关。

结论

N蛋白水平可为COVID-19疾病进展和预后提供见解。需要进一步研究以探索这些发现的临床意义,从而优化患者护理并改善结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0259/12035297/8538c7db7241/10.1177_20499361251333617-fig1.jpg

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