Evidence map›Paper›PMID 36400804›Full record

ArticleScientific reports2022

Diminished neutralization responses towards SARS-CoV-2 Omicron VoC after mRNA or vector-based COVID-19 vaccinations.

Henning Jacobsen, Monika Strengert, Henrike Maaß, Mario Alberto Ynga Durand, Maeva Katzmarzyk, Barbora Kessel, Manuela Harries, Ulfert Rand, Leila Abassi, Yeonsu Kim and 20 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 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

30 authors at 6 institutions in 1 country.

Henning Jacobsen *Department of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Monika Strengert *Department of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Henrike MaaßDepartment of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Mario Alberto Ynga DurandDepartment of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Maeva KatzmarzykDepartment of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Barbora KesselDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Manuela HarriesDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Ulfert RandDepartment of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Leila AbassiDepartment of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Yeonsu KimDepartment of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Tatjana LüddeckeDepartment of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Kristin MetzdorfDepartment of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Pilar HernandezDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Julia OrtmannDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Jana-Kristin HeiseDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Stefanie CastellDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Daniela GornykDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Stephan GlöcknerDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Vanessa MelhornDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Yvonne KemmlingDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Berit LangeDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Alex DulovicNMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, Germany.
Patrick MarsallNMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, Germany.
Julia HäringNMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, Germany.
Daniel JunkerNMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, Germany.
Nicole Schneiderhan-MarraNMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, Germany.
Markus HoffmannDeutsches Primatenzentrum, Leibniz-Institut Für Primatenforschung, Göttingen, Germany.
Stefan PöhlmannDeutsches Primatenzentrum, Leibniz-Institut Für Primatenforschung, Göttingen, Germany.
Gérard KrauseDepartment of Epidemiology, Helmholtz Centre for Infection Research, Braunschweig, Germany. Gerard.Krause@helmholtz-hzi.de.
Luka Cicin-SainDepartment of Viral Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany. luka.cicin-sain@helmholtz-hzi.de.
Helmholtz Centre for Infection Research · DEUniversity of Tübingen · DECenter for Experimental and Clinical Infection Research · DEGerman Center for Infection Research · DEGerman Primate Center · DEUniversity of Göttingen · DE

Funding

Bundesministerium für Bildung und Forschung 01KI2006DBundesministerium für Bildung und Forschung 01KI20328ABundesministerium für Bildung und Forschung 01KX2021Deutsche Forschungsgemeinschaft 39087428Deutsche Forschungsgemeinschaft PO 716/11-1, PO 716/14-1Helmholtz-Gemeinschaft KA1-Co-02Helmholtz-Gemeinschaft SO-96Niedersächsisches Ministerium für Wissenschaft und Kultur 14-76103-184Niedersächsisches Ministerium für Wissenschaft und Kultur MWK HZI COVID-19
6 · The paper itself

Abstract

SARS-CoV-2 variants accumulating immune escape mutations provide a significant risk to vaccine-induced protection against infection. The novel variant of concern (VoC) Omicron BA.1 and its sub-lineages have the largest number of amino acid alterations in its Spike protein to date. Thus, they may efficiently escape recognition by neutralizing antibodies, allowing breakthrough infections in convalescent and vaccinated individuals in particular in those who have only received a primary immunization scheme. We analyzed neutralization activity of sera from individuals after vaccination with all mRNA-, vector- or heterologous immunization schemes currently available in Europe by in vitro neutralization assay at peak response towards SARS-CoV-2 B.1, Omicron sub-lineages BA.1, BA.2, BA.2.12.1, BA.3, BA.4/5, Beta and Delta pseudotypes and also provide longitudinal follow-up data from BNT162b2 vaccinees. All vaccines apart from Ad26.CoV2.S showed high levels of responder rates (96-100%) towards the SARS-CoV-2 B.1 isolate, and minor to moderate reductions in neutralizing Beta and Delta VoC pseudotypes. The novel Omicron variant and its sub-lineages had the biggest impact, both in terms of response rates and neutralization titers. Only mRNA-1273 showed a 100% response rate to Omicron BA.1 and induced the highest level of neutralizing antibody titers, followed by heterologous prime-boost approaches. Homologous BNT162b2 vaccination, vector-based AZD1222 and Ad26.CoV2.S performed less well with peak responder rates of 48%, 56% and 9%, respectively. However, Omicron responder rates in BNT162b2 recipients were maintained in our six month longitudinal follow-up indicating that individuals with cross-protection against Omicron maintain it over time. Overall, our data strongly argue for booster doses in individuals who were previously vaccinated with BNT162b2, or a vector-based primary immunization scheme.

Indexed as

COVID-19SARS-CoV-2Ad26COVS1Antibodies, ViralBNT162 VaccineChAdOx1 nCoV-19COVID-19 VaccinesHumansNeutralization TestsRNA, MessengerVaccinationAd26COVS1Antibodies, ViralBNT162 VaccineChAdOx1 nCoV-19COVID-19 VaccinesRNA, Messenger

Identifiers

PMID36400804
PMCPMC9673895
OpenAlexW4309473723

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.