Evidence map›Paper›PMID 36293090›Full record

ArticleInternational journal of molecular sciences2022

Comparative Analysis of Antibody Titers against the Spike Protein of SARS-CoV-2 Variants in Infected Patient Cohorts and Diverse Vaccination Regimes.

Alexandru Odainic, Jasper Spitzer, Jennifer Barbara Szlapa, Simon Schade, Tim Jonas Krämer, Jakob Neuberger, Christian Bode, Folkert Steinhagen, Ricarda Maria Schmithausen, Gero Wilbring and 20 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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  2. Review
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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

30 authors at 7 institutions in 4 countries.

Alexandru OdainicInstitute of Innate Immunity, University Hospital Bonn, 53127 Bonn, Germany.
Jasper SpitzerInstitute of Innate Immunity, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0001-9696-2092
Jennifer Barbara SzlapaInstitute of Experimental Immunology, University Hospital Bonn, 53127 Bonn, Germany.
Simon SchadeInstitute of Innate Immunity, University Hospital Bonn, 53127 Bonn, Germany.
Tim Jonas KrämerInstitute of Innate Immunity, University Hospital Bonn, 53127 Bonn, Germany.
Jakob NeubergerInstitute of Innate Immunity, University Hospital Bonn, 53127 Bonn, Germany.
Christian BodeDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0002-0830-870X
Folkert SteinhagenDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Bonn, 53127 Bonn, Germany.
Ricarda Maria SchmithausenInstitute for Hygiene and Public Health, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0002-3736-8672
Gero WilbringInstitute for Hygiene and Public Health, University Hospital Bonn, 53127 Bonn, Germany.
Esther SibInstitute for Hygiene and Public Health, University Hospital Bonn, 53127 Bonn, Germany.
Nico Tom MuttersInstitute for Hygiene and Public Health, University Hospital Bonn, 53127 Bonn, Germany.
Frederik RabenschlagMedical Corps of the German Armed Forces, German Armed Forces Central Hospital, 56072 Koblenz, Germany.
Lisa KettelMedical Corps of the German Armed Forces, German Armed Forces Central Hospital, 56072 Koblenz, Germany.
Maike WoznitzaMedical Corps of the German Armed Forces, German Armed Forces Central Hospital, 56072 Koblenz, Germany.
Kathrin van BremenDepartment of Internal Medicine I, University Hospital Bonn, 53127 Bonn, Germany.
Tina PeersClare Park Hospital, Farnham GU10 5XX, UK.
Gez MedingerDepartment of Paramedic Science, School of Health and Social Work, University of Hertfordshire, Hatfield AL10 9AB, UK.
Anushka KudaliyanageInstitute of Innate Immunity, University Hospital Bonn, 53127 Bonn, Germany.
Maike KreutzenbeckInstitute of Innate Immunity, University Hospital Bonn, 53127 Bonn, Germany.
Ulrike StrubeInstitute of Innate Immunity, University Hospital Bonn, 53127 Bonn, Germany.
Joseph M JohnsonQuanterix Corporation, Billerica, MA 01821, USA.
Dawn MattoonQuanterix Corporation, Billerica, MA 01821, USA.
Andrew J BallQuanterix Corporation, Billerica, MA 01821, USA.ORCID 0000-0002-5320-9364
Stefan ScoryMeso Scale Diagnostics, Rockville, MD 20850, USA.
Richard McGuireMeso Scale Diagnostics, Rockville, MD 20850, USA.
Christian PutensenDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Bonn, 53127 Bonn, Germany.
Zeinab AbdullahInstitute of Experimental Immunology, University Hospital Bonn, 53127 Bonn, Germany.
Catharina LatzDardenne Eye Hospital, 53177 Bonn, Germany.ORCID 0000-0002-8003-4547
Susanne Viktoria SchmidtInstitute of Innate Immunity, University Hospital Bonn, 53127 Bonn, Germany.
University Hospital Bonn · DEBundeswehrzentralkrankenhaus Koblenz · DEQuanterix (United States) · USMeso Scale Discovery (United States) · USSpire Clare Park Hospital · GBThe University of Melbourne · AUUniversity of Hertfordshire · GB

Funding

Federal Ministry of Education and Research 01KI20343
6 · The paper itself

Abstract

The presence of neutralizing antibodies against SARS-CoV-2 correlates with protection against infection and severe COVID-19 disease courses. Understanding the dynamics of antibody development against the SARS-CoV-2 virus is important for recommendations on vaccination strategies and on control of the COVID-19 pandemic. This study investigates the dynamics and extent of α-Spike-Ab development by different vaccines manufactured by Johnson & Johnson, AstraZeneca, Pfizer-BioNTech and Moderna. On day 1 after vaccination, we observed a temporal low-grade inflammatory response. α-Spike-Ab titers were reduced after six months of vaccination with mRNA vaccines and increased 14 days after booster vaccinations to a maximum that exceeded titers from mild and critical COVID-19 and Long-COVID patients. Within the group of critical COVID-19 patients, we observed a trend for lower α-Spike-Ab titers in the group of patients who survived COVID-19. This trend accompanied higher numbers of pro-B cells, fewer mature B cells and a higher frequency of T follicular helper cells. Finally, we present data demonstrating that past infection with mild COVID-19 does not lead to long-term increased Ab titers and that even the group of previously infected SARS-CoV-2 patients benefit from a vaccination six months after the infection.

Indexed as

COVID-19SARS-CoV-2Antibodies, NeutralizingAntibodies, ViralHumansPandemicsSpike Glycoprotein, CoronavirusVaccinationViral Envelope ProteinsAntibodies, NeutralizingAntibodies, ViralSpike Glycoprotein, CoronavirusViral Envelope Proteinsantibody responseinflammationLong-COVIDlymphocytesSARS-CoV-2vaccination

Identifiers

PMID36293090
PMCPMC9602709
OpenAlexW4306152098

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.