Evidence map›Paper›PMID 33965698›Full record

ArticleJournal of clinical virology : the official publication of the Pan American Society for Clinical Virology2021

Lack of antibodies against seasonal coronavirus OC43 nucleocapsid protein identifies patients at risk of critical COVID-19.

Martin Dugas, Tanja Grote-Westrick, Uta Merle, Michaela Fontenay, Andreas E Kremer, Frank Hanses, Richard Vollenberg, Eva Lorentzen, Shilpa Tiwari-Heckler, Jérôme Duchemin and 10 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.1field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 54 citations in OpenAlex.

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  9. Cell surface nucleocapsid protein expression: A betacoronavirus immunomodulatory strategy.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  17. Impact of cross-coronavirus immunity in post-acute sequelae of COVID-19.medRxiv : the preprint server for health sciences · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 7 institutions in 2 countries.

Martin DugasInstitute of Medical Informatics, University of Münster, Germany. Electronic address: dugas@uni-muenster.de.
Tanja Grote-WestrickInstitute of Virology, Department of Clinical Virology, University Hospital Münster, Germany. Electronic address: t_grot07@uni-muenster.de.
Uta MerleMedizinische Klinik, Abteilung Innere Medizin IV, University Hospital Heidelberg, Germany. Electronic address: Uta.Merle@med.uni-heidelberg.de.
Michaela FontenayAssistance Publique-Hôpitaux de Paris, AP-HP. Centre-Université de Paris, Hôpital Cochin, Service d'hématologie biologique, Paris, France; Université de Paris, Institut Cochin, CNRS UMR8104, INSERM, Paris U1016, France. Electronic address: michaela.fontenay@aphp.fr.
Andreas E KremerDepartment of Medicine 1, University Hospital Erlangen and Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany. Electronic address: andreas.kremer@uk-erlangen.de.
Frank HansesEmergency Department, University Hospital Regensburg, Germany; Department for Infectious Diseases and Infection Control, University Hospital Regensburg, Germany. Electronic address: frank.hanses@klinik.uni-regensburg.de.
Richard VollenbergMedizinische Klinik B (Gastroenterologie, Hepatologie, Endokrinologie, Klinische Infektiologie), University Hospital Münster, Germany. Electronic address: Richard.Vollenberg@ukmuenster.de.
Eva LorentzenInstitute of Virology, Department of Clinical Virology, University Hospital Münster, Germany. Electronic address: Eva.Lorentzen@uni-muenster.de.
Shilpa Tiwari-HecklerMedizinische Klinik, Abteilung Innere Medizin IV, University Hospital Heidelberg, Germany. Electronic address: Shilpa.Tiwari-Heckler@med.uni-heidelberg.de.
Jérôme DucheminAssistance Publique-Hôpitaux de Paris, AP-HP. Centre-Université de Paris, Hôpital Cochin, Service d'hématologie biologique, Paris, France. Electronic address: jerome.duchemin@aphp.fr.
Syrine EllouzeAssistance Publique-Hôpitaux de Paris, AP-HP. Centre-Université de Paris, Hôpital Cochin, Service d'hématologie biologique, Paris, France. Electronic address: syrine.ellouze@aphp.fr.
Marcel VetterDepartment of Medicine 1, University Hospital Erlangen and Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany. Electronic address: Marcel.Vetter@uk-erlangen.de.
Julia FürstDepartment of Medicine 1, University Hospital Erlangen and Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany. Electronic address: Julia.Fuerst@uk-erlangen.de.
Philipp SchusterInstitute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany. Electronic address: Philipp1.Schuster@klinik.uni-regensburg.de.
Tobias BrixInstitute of Medical Informatics, University of Münster, Germany. Electronic address: tobias.brix@uni-muenster.de.
Claudia M DenkingerDivision of Tropical Medicine, Center of Infectious Diseases, University Hospital Heidelberg, Germany; German Centre for Infection Research (DZIF), partner site Heidelberg University Hospital, Heidelberg, Germany. Electronic address: Claudia.Denkinger@uni-heidelberg.de.
Carsten Müller-TidowMedizinische Klinik, Abteilung Innere Medizin V, University Hospital Heidelberg, Germany. Electronic address: Carsten.Mueller-Tidow@med.uni-heidelberg.de.
Hartmut SchmidtMedizinische Klinik B (Gastroenterologie, Hepatologie, Endokrinologie, Klinische Infektiologie), University Hospital Münster, Germany. Electronic address: hepar@ukmuenster.de.
Phil-Robin TepasseMedizinische Klinik B (Gastroenterologie, Hepatologie, Endokrinologie, Klinische Infektiologie), University Hospital Münster, Germany. Electronic address: phil-robin.tepasse@ukmuenster.de.
Joachim KühnInstitute of Virology, Department of Clinical Virology, University Hospital Münster, Germany. Electronic address: Joachim.Kuehn@ukmuenster.de.
University Hospital Münster · DEHeidelberg University · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversité Paris Cité · FRUniversity Hospital Regensburg · DEUniversity of Münster · DECentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe vast majority of COVID-19 patients experience a mild disease. However, a minority suffers from critical disease with substantial morbidity and mortality.

objectivesTo identify individuals at risk of critical COVID-19, the relevance of a seroreactivity against seasonal human coronaviruses was analyzed.

methodsWe conducted a multi-center non-interventional study comprising 296 patients with confirmed SARS-CoV-2 infections from four tertiary care referral centers in Germany and France. The ICU group comprised more males, whereas the outpatient group contained a higher percentage of females. For each patient, the serum or plasma sample obtained closest after symptom onset was examined by immunoblot regarding IgG antibodies against the nucleocapsid protein (NP) of HCoV 229E, NL63, OC43 and HKU1.

resultsMedian age was 60 years (range 18-96). Patients with critical disease (n=106) had significantly lower levels of anti-HCoV OC43 nucleocapsid protein (NP)-specific antibodies compared to other COVID-19 inpatients (p=0.007). In multivariate analysis (adjusted for age, sex and BMI), OC43 negative inpatients had an increased risk of critical disease (adjusted odds ratio (AOR) 2.68 [95% CI 1.09 - 7.05]), higher than the risk by increased age or BMI, and lower than the risk by male sex. A risk stratification based on sex and OC43 serostatus was derived from this analysis.

conclusionsOur results suggest that prior infections with seasonal human coronaviruses can protect against a severe course of COVID-19. Therefore, anti-OC43 antibodies should be measured for COVID-19 inpatients and considered as part of the risk assessment for each patient. Hence, we expect individuals tested negative for anti-OC43 antibodies to particularly benefit from vaccination against SARS-CoV-2, especially with other risk factors prevailing.

Indexed as

AdolescentAdultAgedAged, 80 and overAntibodies, ViralCoronavirus Nucleocapsid ProteinsCOVID-19FemaleHumansImmunoglobulin GMaleMiddle AgedPhosphoproteinsRisk FactorsSARS-CoV-2Young AdultAntibodies, ViralCoronavirus Nucleocapsid ProteinsImmunoglobulin Gnucleocapsid phosphoprotein, SARS-CoV-2PhosphoproteinsCOVID-19Critical diseaseOC43SARS-CoV-2Seasonal coronavirus

Identifiers

PMID33965698
PMCPMC8065244
OpenAlexW3158186844

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.