Evidence map›Paper›PMID 36005839›Full record

ArticleMicrobiology spectrum2022

Reduced Sensitivity of Commercial Spike-Specific Antibody Assays after Primary Infection with the SARS-CoV-2 Omicron Variant.

David Niklas Springer, Thomas Perkmann, Claudia Maria Jani, Patrick Mucher, Katja Prüger, Rodrig Marculescu, Elisabeth Reuberger, Jeremy Vann Camp, Marianne Graninger, Christian Borsodi and 9 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 37 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

19 authors at 2 institutions in 1 country.

David Niklas SpringerCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Thomas PerkmannDepartment of Laboratory Medicine, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Claudia Maria JaniCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Patrick MucherDepartment of Laboratory Medicine, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Katja PrügerCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Rodrig MarculescuDepartment of Laboratory Medicine, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Elisabeth ReubergerCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Jeremy Vann CampCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Marianne GraningerCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Christian BorsodiCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Josef DeutschPrivate Practice, Völkermarkt, Austria.
Oliver LammelPrivate Practice, Ramsau am Dachstein, Austria.
Stephan Walter AberleCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Elisabeth Puchhammer-StöcklCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.ORCID 0000-0002-0673-8335
Helmuth HaslacherDepartment of Laboratory Medicine, Medical University of Viennagrid.22937.3d, Vienna, Austria.ORCID 0000-0003-4605-2503
Eva HöltlCenter for Public Health, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Judith Helene AberleCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.
Karin StiasnyCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.ORCID 0000-0002-1902-8674
Lukas WeseslindtnerCenter for Virology, Medical University of Viennagrid.22937.3d, Vienna, Austria.ORCID 0000-0001-8950-937X
Medical University of Vienna · ATLKH Hochsteiermark · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SARS-CoV-2 Omicron variant is characterized by substantial changes in the antigenic structure of the Spike (S) protein. Therefore, antibodies induced by primary Omicron infection lack neutralizing activity against earlier variants. In this study, we analyzed whether these antigenic changes impact the sensitivity of commercial anti-SARS-CoV-2 antibody assays. Sera from 37 unvaccinated, convalescent individuals after putative primary Omicron infection were tested with a panel of 20 commercial anti-SARS-CoV-2 immunoassays. As controls, we used samples from 43 individuals after primary infection with the SARS-CoV-2 ancestral wild-type strain. In addition, variant-specific live-virus neutralization assays were used as a reference for the presence of SARS-CoV-2-specific antibodies in the samples. Notably, in Omicron convalescents, there was a statistically significant reduction in the sensitivity of all antibody assays containing S or its receptor-binding-domain (RBD) as antigens. Furthermore, antibody levels quantified by these assays displayed a weaker correlation with Omicron-specific neutralizing antibody titers than with those against the wild type. In contrast, the sensitivity of nucleocapsid-protein-specific immunoassays was similar in wild-type and Omicron-infected subjects. In summary, the antigenic changes in the Omicron S lead to reduced immunoreactivity in the current commercial S- and RBD-specific antibody assays, impairing their diagnostic performance.

Indexed as

COVID-19Spike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralHumansMembrane GlycoproteinsNeutralization TestsSARS-CoV-2Viral Envelope ProteinsAntibodies, NeutralizingAntibodies, ViralMembrane GlycoproteinsSpike Glycoprotein, CoronavirusViral Envelope Proteinsantibodiesantibody assayimmunoassayneutralizationOmicronSARS-CoV-2sensitivitysurrogate assay

Identifiers

PMID36005839
PMCPMC9603218
OpenAlexW4293089331

What Socratic 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 Socratic graph.