Evidence map›Paper›PMID 40297751›Full record

ArticleTherapeutic advances in infectious disease

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.

Alfredo J Mena Lora, Kimi Enders, Huimin Wu, Luis Parra-Rodriguez, Christopher Palma, Katy Saliba, Sylvain Laverdurre, P Brian Smith, Kevin J Anstrom, Samuel A Bozzette and 1 more

Abstract read
In one paragraph

Article in Therapeutic advances in infectious disease. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Alfredo J Mena LoraDivision of Infectious Diseases, University of Illinois at Chicago, 808 S Wood St, RM 888, Chicago, IL 60612, USA.ORCID https://orcid.org/0000-0002-8337-757X
Kimi EndersUniversity of North Carolina, Chapel Hill, NC, USA.
Huimin WuUniversity of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Luis Parra-RodriguezWashington University School of Medicine in St. Louis, St. Louis, MO, USA.
Christopher PalmaUniversity of Rochester, Rochester, NY, USA.
Katy SalibaNational Institute of Allergy and Infectious Diseases, Bethesda, MD, USA.
Sylvain LaverdurreLeidos Biomedical Research, Bethesda, MD, USA.
P Brian SmithDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Kevin J AnstromUniversity of North Carolina, Chapel Hill, NC, USA.
Samuel A BozzetteNational Center for Advancing Translational Sciences, Bethesda, MD, USA.
William G PowderlyWashington University School of Medicine in St. Louis, St. Louis, MO, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

abataceptcenicrivirocCOVID-19infliximabN-proteinserology

Identifiers

PMID40297751
PMCPMC12035297

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