Evidence map›Paper›PMID 35928813›Full record

ArticleFrontiers in immunology2022

Different Neutralization Profiles After Primary SARS-CoV-2 Omicron BA.1 and BA.2 Infections.

Iris Medits, David N Springer, Marianne Graninger, Jeremy V Camp, Eva Höltl, Stephan W Aberle, Marianna T Traugott, Wolfgang Hoepler, Josef Deutsch, Oliver Lammel and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.1field-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

22 citing papers in PubMed, 41 citations in OpenAlex.

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  19. Imprinted antibody responses against SARS-CoV-2 Omicron sublineages.bioRxiv : the preprint server for biology · 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

16 authors at 1 institution in 1 country.

Iris MeditsCenter for Virology, Medical University of Vienna, Vienna, Austria.
David N SpringerCenter for Virology, Medical University of Vienna, Vienna, Austria.
Marianne GraningerCenter for Virology, Medical University of Vienna, Vienna, Austria.
Jeremy V CampCenter for Virology, Medical University of Vienna, Vienna, Austria.
Eva HöltlCenter for Public Health, Medical University of Vienna, Vienna, Austria.
Stephan W AberleCenter for Virology, Medical University of Vienna, Vienna, Austria.
Marianna T TraugottDepartment of Medicine IV, Clinic Favoriten, Vienna Healthcare Group, Vienna, Austria.
Wolfgang HoeplerDepartment of Medicine IV, Clinic Favoriten, Vienna Healthcare Group, Vienna, Austria.
Josef DeutschPractice Dr. Deutsch, Völkermarkt, Austria.
Oliver LammelPractice Dr. Lammel, Ramsau am Dachstein, Austria.
Christian BorsodiCenter for Virology, Medical University of Vienna, Vienna, Austria.
Elisabeth Puchhammer-StöcklCenter for Virology, Medical University of Vienna, Vienna, Austria.
Alexander ZoufalyDepartment of Medicine IV, Clinic Favoriten, Vienna Healthcare Group, Vienna, Austria.
Lukas WeseslindtnerCenter for Virology, Medical University of Vienna, Vienna, Austria.
Judith H AberleCenter for Virology, Medical University of Vienna, Vienna, Austria.
Karin StiasnyCenter for Virology, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Methods: The SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) Omicron (B.1.1.529) variant is the antigenically most distinct variant to date. As the heavily mutated spike protein enables neutralization escape, we studied serum-neutralizing activities of naïve and vaccinated individuals after Omicron BA.1 or BA.2 sub-lineage infections in live virus neutralization tests with Omicron BA.1, Omicron BA.2, wildtype (WT, B1.1), and Delta (B.1.617.2) strains. Serum samples obtained after WT infections and three-dose mRNA vaccinations with and without prior infection were included as controls. Results: Primary BA.1 infections yielded reduced neutralizing antibody levels against WT, Delta, and Omicron BA.2, while samples from BA.2-infected individuals showed almost no cross-neutralization against the other variants. Serum neutralization of Omicron BA.1 and BA.2 variants was detectable after three-dose mRNA vaccinations, but with reduced titers. Vaccination-breakthrough infections with either Omicron BA.1 or BA.2, however, generated equal cross-neutralizing antibody levels against all SARS-CoV-2 variants tested. Conclusions: Our study demonstrates that although Omicron variants are able to enhance cross-neutralizing antibody levels in pre-immune individuals, primary infections with BA.1 or BA.2 induced mostly variant-specific neutralizing antibodies, emphasizing the differently shaped humoral immunity induced by the two Omicron variants. These data thus contribute substantially to the understanding of antibody responses induced by primary Omicron infections or multiple exposures to different SARS-CoV-2 variants and are of particular importance for developing vaccination strategies in the light of future emerging variants.

Indexed as

COVID-19SARS-CoV-2Antibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesHumansMembrane GlycoproteinsNeutralization TestsRNA, MessengerSpike Glycoprotein, CoronavirusViral Envelope ProteinsAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesMembrane GlycoproteinsRNA, MessengerSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Viral Envelope Proteinsimmune escapeOmicron sub-lineagesSARS-CoV-2SARS-CoV-2 neutralizationSARS-CoV-2 variant of concern

Identifiers

PMID35928813
PMCPMC9344875
OpenAlexW4285797594

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.