Evidence map›Paper›PMID 36622205›Full record

ArticleMicrobiology spectrum2023

Comprehensive Comparison of Seven SARS-CoV-2-Specific Surrogate Virus Neutralization and Anti-Spike IgG Antibody Assays Using a Live-Virus Neutralization Assay as a Reference.

Marianne Graninger, Claudia Maria Jani, Elisabeth Reuberger, Katja Prüger, Philipp Gaspar, David Niklas Springer, Christian Borsodi, Lisa Weidner, Susanne Rabady, Elisabeth Puchhammer-Stöckl and 5 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 35 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

15 authors at 3 institutions in 1 country.

Marianne GraningerCenter for Virology, Medical University of Vienna, Vienna, Austria.
Claudia Maria JaniCenter for Virology, Medical University of Vienna, Vienna, Austria.
Elisabeth ReubergerCenter for Virology, Medical University of Vienna, Vienna, Austria.
Katja PrügerCenter for Virology, Medical University of Vienna, Vienna, Austria.
Philipp GasparCenter for Virology, Medical University of Vienna, Vienna, Austria.
David Niklas SpringerCenter for Virology, Medical University of Vienna, Vienna, Austria.
Christian BorsodiCenter for Virology, Medical University of Vienna, Vienna, Austria.
Lisa WeidnerAustrian Red Cross, Blood Service for Vienna, Lower Austria, and Burgenland, Vienna, Austria.
Susanne RabadyKarl Landsteiner University of Health Sciences, Department of General Health Studies, Division General and Family Medicine, Krems, Austria.
Elisabeth Puchhammer-StöcklCenter for Virology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-0673-8335
Christof JungbauerAustrian Red Cross, Blood Service for Vienna, Lower Austria, and Burgenland, Vienna, Austria.
Eva HöltlCenter for Public Health, Medical University of Vienna, Vienna, Austria.
Judith Helene AberleCenter for Virology, Medical University of Vienna, Vienna, Austria.
Karin Stiasny *Center for Virology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-1902-8674
Lukas Weseslindtner *Center for Virology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-8950-937X
Medical University of Vienna · ATAustrian Red Cross · ATKarl Landsteiner University of Health Sciences · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutralizing antibodies (nAbs) are considered a valuable marker for measuring humoral immunity against SARS-CoV-2. However, live-virus neutralization tests (NTs) require high-biosafety-level laboratories and are time-consuming. Therefore, surrogate virus neutralization tests (sVNTs) have been widely applied, but unlike most anti-spike (S) antibody assays, NTs and sVNTs are not harmonized, requiring further evaluation and comparative analyses. This study compared seven commercial sVNTs and anti-S-antibody assays with a live-virus NT as a reference, using a panel of 720 single and longitudinal serum samples from 666 convalescent patients after SARS-CoV-2 infection. The sensitivity of these assays for detecting antibodies ranged from 48 to 94% after PCR-confirmed infection and from 56% to 100% relative to positivity in the in-house live-virus NT. Furthermore, we performed receiver operating characteristic (ROC) curve analyses to determine which immunoassays were most suitable for assessing nAb titers exceeding a specific cutoff (NT titer, ≥80) and found that the NeutraLISA and the cPass assays reached the highest area under the curve (AUC), exceeding 0.91. In addition, when the assays were compared for their correlation with nAb kinetics over time in a set of longitudinal samples, the extent of the measured decrease of nAbs after infection varied widely among the evaluated immunoassays. Finally, in vaccinated convalescent patients, high titers of nAbs exceeded the upper limit of the evaluated assays' quantification ranges. Based on data from this study, we conclude that commercial immunoassays are acceptable substitutes for live-virus NTs, particularly when additional adapted cutoffs are employed to detect nAbs beyond a specific threshold titer.

Indexed as

COVID-19SARS-CoV-2Antibodies, NeutralizingAntibodies, ViralHumansImmunoglobulin GNeutralization TestsAntibodies, NeutralizingAntibodies, ViralImmunoglobulin GantibodiesassayimmunoassaysmicroarrayneutralizationneutralizingSARS-CoV-2surrogate

Identifiers

PMID36622205
PMCPMC9927416
OpenAlexW4313857696

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.