Evidence map›Paper›PMID 35090165›Full record

ArticleNature medicine2022

Three exposures to the spike protein of SARS-CoV-2 by either infection or vaccination elicit superior neutralizing immunity to all variants of concern.

Paul R Wratil, Marcel Stern, Alina Priller, Annika Willmann, Giovanni Almanzar, Emanuel Vogel, Martin Feuerherd, Cho-Chin Cheng, Sarah Yazici, Catharina Christa and 27 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 174 papers.

0numbers the graph read from it
0cells of the map it votes in
174citing papers in PubMed
28.0field-weighted citation impact, top 1% 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

174 citing papers in PubMed, 282 citations in OpenAlex.

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114 more citing papers are in PubMed but not listed here.

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

37 authors at 7 institutions in 2 countries.

Paul R Wratil *Max von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Munich, Germany.
Marcel Stern *Max von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Munich, Germany.ORCID http://orcid.org/0000-0002-7692-6905
Alina Priller *Institute of Molecular Immunology and Experimental Oncology, University Hospital rechts der Isar, Technical University of Munich (TUM), School of Medicine, Munich, Germany.ORCID http://orcid.org/0000-0002-4982-0347
Annika WillmannInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.
Giovanni AlmanzarPediatric Rheumatology / Special Immunology, Pediatrics Department, University Hospital Würzburg, Würzburg, Germany.
Emanuel VogelInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.ORCID http://orcid.org/0000-0001-6560-0136
Martin FeuerherdInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.ORCID http://orcid.org/0000-0002-5272-6503
Cho-Chin ChengInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.
Sarah YaziciInstitute of Molecular Immunology and Experimental Oncology, University Hospital rechts der Isar, Technical University of Munich (TUM), School of Medicine, Munich, Germany.
Catharina ChristaInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.
Samuel JeskeInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.
Gaia LupoliMax von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Munich, Germany.ORCID http://orcid.org/0000-0002-2786-6627
Tim VogtPediatric Rheumatology / Special Immunology, Pediatrics Department, University Hospital Würzburg, Würzburg, Germany.
Manuel AlbaneseMax von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Munich, Germany.ORCID http://orcid.org/0000-0002-4614-7599
Ernesto Mejías-PérezMax von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Munich, Germany.ORCID http://orcid.org/0000-0002-5208-8177
Stefan BauernfriedGene Center and Department of Biochemistry, LMU München, Munich, Germany.ORCID http://orcid.org/0000-0003-1910-5032
Natalia GrafInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.
Hrvoje MijocevicInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.
Martin VuInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.
Kathrin TinnefeldInstitute of Virology, Helmholtz Center Munich, TUM, School of Medicine, Munich, Germany.
Jochen WettengelGerman Centre for Infection Research (DZIF), Partner Site, Munich, Germany.
Dieter HoffmannGerman Centre for Infection Research (DZIF), Partner Site, Munich, Germany.
Maximilian MuenchhoffMax von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Munich, Germany.ORCID http://orcid.org/0000-0001-7016-0470
Christopher DaechertMax von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Munich, Germany.ORCID http://orcid.org/0000-0001-6441-3099
Helga MairhoferMax von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Munich, Germany.
Stefan KrebsLaboratory for Functional Genome Analysis, Gene Center, LMU München, Munich, Germany.
Volker FingerleBavarian Health and Food Safety Authority (LGL), Oberschleißheim, Germany.
Alexander GrafLaboratory for Functional Genome Analysis, Gene Center, LMU München, Munich, Germany.
Philipp SteiningerInstitute of Clinical and Molecular Virology, University Hospital Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany.
Helmut BlumLaboratory for Functional Genome Analysis, Gene Center, LMU München, Munich, Germany.ORCID http://orcid.org/0000-0002-3994-2332
Veit HornungGene Center and Department of Biochemistry, LMU München, Munich, Germany.ORCID http://orcid.org/0000-0002-4150-194X
Bernhard LieblBavarian Health and Food Safety Authority (LGL), Oberschleißheim, Germany.
Klaus ÜberlaInstitute of Clinical and Molecular Virology, University Hospital Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany.
Martina PrelogPediatric Rheumatology / Special Immunology, Pediatrics Department, University Hospital Würzburg, Würzburg, Germany.
Percy KnolleGerman Centre for Infection Research (DZIF), Partner Site, Munich, Germany. percy.knolle@tum.de.ORCID http://orcid.org/0000-0003-2983-0414
Oliver T KepplerMax von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, LMU München, Munich, Germany. Keppler@mvp.uni-muenchen.de.ORCID http://orcid.org/0000-0002-1384-8946
Ulrike ProtzerGerman Centre for Infection Research (DZIF), Partner Site, Munich, Germany. protzer@tum.de.ORCID http://orcid.org/0000-0002-9421-1911
Helmholtz Zentrum München · DELudwig-Maximilians-Universität München · DETUM Klinikum · DEUniversitätsklinikum Würzburg · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEGerman Center for Infection Research · DELMU Klinikum · DE

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) TRR179Helmholtz Association CoViPa consortium
6 · The paper itself

Abstract

Infection-neutralizing antibody responses after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or coronavirus disease 2019 vaccination are an essential component of antiviral immunity. Antibody-mediated protection is challenged by the emergence of SARS-CoV-2 variants of concern (VoCs) with immune escape properties, such as omicron (B.1.1.529), which is rapidly spreading worldwide. Here we report neutralizing antibody dynamics in a longitudinal cohort of coronavirus disease 2019 convalescent and infection-naive individuals vaccinated with mRNA BNT162b2 by quantifying SARS-CoV-2 spike protein antibodies and determining their avidity and neutralization capacity in serum. Using live-virus neutralization assays, we show that a superior infection-neutralizing capacity against all VoCs, including omicron, developed after either two vaccinations in convalescents or a third vaccination or breakthrough infection of twice-vaccinated, naive individuals. These three consecutive spike antigen exposures resulted in an increasing neutralization capacity per anti-spike antibody unit and were paralleled by stepwise increases in antibody avidity. We conclude that an infection-plus-vaccination-induced hybrid immunity or a triple immunization can induce high-quality antibodies with superior neutralization capacity against VoCs, including omicron.

Indexed as

BNT162 VaccineCOVID-19SARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralHumansVaccinationAntibodies, NeutralizingAntibodies, ViralBNT162 VaccineSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID35090165
OpenAlexW4210654369

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.