Evidence map›Paper›PMID 35079775›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2022

Severe Acute Respiratory Syndrome Coronavirus 2 Vaccination Boosts Neutralizing Activity Against Seasonal Human Coronaviruses.

Jan Lawrenz, Qinya Xie, Fabian Zech, Tatjana Weil, Alina Seidel, Daniela Krnavek, Lia van der Hoek, Jan Münch, Janis A Müller, Frank Kirchhoff

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

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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

10 authors at 2 institutions in 2 countries.

Jan LawrenzInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Qinya XieInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Fabian ZechInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Tatjana WeilInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Alina SeidelInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Daniela KrnavekInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Lia van der HoekLaboratory of Experimental Virology, Department of Medical Microbiology, Amsterdam UMC, Location AMC, University of Amsterdam, Amsterdam, The Netherlands.
Jan MünchInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Janis A MüllerInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.ORCID 0000-0002-0347-416X
Frank KirchhoffInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.ORCID 0000-0002-7052-2360
Universität Ulm · DEAmsterdam University Medical Centers · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMost of the millions of people that are vaccinated against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease 2019 (COVID-19), have previously been infected by related circulating human coronaviruses (hCoVs) causing common colds and will experience further encounters with these viruses in the future. Whether COVID-19 vaccinations impact neutralization of seasonal coronaviruses is largely unknown.

methodsWe analyzed the capacity of sera derived from 24 individuals before and after heterologous ChAdOx1 nCoV-19 BNT162b2 prime-boost vaccination to neutralize genuine OC43, NL63, and 229E hCoVs, as well as viral pseudoparticles carrying the SARS-CoV-1, SARS-CoV-2, Middle East Respiratory Syndrome (MERS)-CoV, and hCoV-OC43, hCoV-NL63, and hCoV-229E spike proteins. Genuine hCoVs or spike containing pseudovirions were incubated with different concentrations of sera and neutralization efficiencies were determined by measuring viral RNA yields, intracellular viral nucleocapsid expression, or reporter gene expression in Huh-7 cells.

resultsAll individuals showed strong preexisting immunity against hCoV-OC43. Neutralization of hCoV-NL63 was more variable and all sera showed only modest inhibitory activity against genuine hCoV-229E. SARS-CoV-2 vaccination resulted in efficient cross-neutralization of SARS-CoV-1 but not of MERS-CoV. On average, vaccination significantly increased the neutralizing activity against genuine hCoV-OC43, hCoV-NL63, and hCoV-229E.

conclusionsHeterologous COVID-19 vaccination may confer some cross-protection against endemic seasonal coronaviruses.

Indexed as

Coronavirus 229E, HumanCoronavirus NL63, HumanCoronavirus OC43, HumanCOVID-19BNT162 VaccineChAdOx1 nCoV-19COVID-19 VaccinesHumansSARS-CoV-2SeasonsVaccinationBNT162 VaccineChAdOx1 nCoV-19COVID-19 VaccinesCOVID-19 vaccinationcross-neutralizationseasonal coronaviruses

Identifiers

PMID35079775
PMCPMC8807272
OpenAlexW4207073452

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.