Evidence map›Paper›PMID 34197839›Full record

ArticleJournal of virological methods2021

Evaluation of spike protein antigens for SARS-CoV-2 serology.

Suraj Jagtap, Ratnasri K, Priyanka Valloly, Rakhi Sharma, Satyaghosh Maurya, Anushree Gaigore, Chitra Ardhya, Dayananda S Biligi, Bapu Koundinya Desiraju, Uma Chandra Mouli Natchu and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virological methods, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 20 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

12 authors at 3 institutions in 1 country.

Suraj JagtapDepartment of Chemical Engineering, Indian Institute of Science, Bangalore, 560012, India.
Ratnasri KCentre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore, 560012, India.
Priyanka VallolyDepartment of Chemical Engineering, Indian Institute of Science, Bangalore, 560012, India.
Rakhi SharmaDepartment of Chemical Engineering, Indian Institute of Science, Bangalore, 560012, India.
Satyaghosh MauryaDepartment of Chemical Engineering, Indian Institute of Science, Bangalore, 560012, India.
Anushree GaigoreDepartment of Chemical Engineering, Indian Institute of Science, Bangalore, 560012, India.
Chitra ArdhyaDepartment of Pathology, Bangalore Medical College and Research Institute, Bangalore, 560002, India.
Dayananda S BiligiDepartment of Pathology, Bangalore Medical College and Research Institute, Bangalore, 560002, India.
Bapu Koundinya DesirajuTranslational Health Science and Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, India.
Uma Chandra Mouli NatchuDivision of Infectious Diseases, St. John's Research Institute, Bangalore, 560034, India.
Deepak Kumar SainiCentre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore, 560012, India; Department of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bangalore, 560012, India.
Rahul RoyDepartment of Chemical Engineering, Indian Institute of Science, Bangalore, 560012, India; Centre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore, 560012, India. Electronic address: rahulroy@iisc.ac.in.
Indian Institute of Science Bangalore · INBangalore Medical College and Research Institute · INTranslational Health Science and Technology Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpike protein domains are being used in various serology-based assays to detect prior exposure to SARS-CoV-2 virus. However, there has been limited comparison of antibody titers against various spike protein antigens among COVID-19 infected patients.

methodsWe compared four spike proteins (RBD, S1, S2 and a stabilized spike trimer (ST)) representing commonly used antigens for their reactivity to human IgG antibodies using indirect ELISA in serum from COVID-19 patients and pre-2020 samples. ST ELISA was also compared against the EUROIMMUN IgG ELISA test. Further, we estimated time appropriate IgG and IgA seropositivity rates in COVID-19 patients using a panel of sera samples collected longitudinally from the day of onset of symptoms (DOS).

resultsAmong the four spike antigens tested, the ST demonstrated the highest sensitivity (86.2 %; 95 % CI: 77.8-91.7 %), while all four antigens showed high specificity to COVID-19 sera (94.7-96.8 %). 13.8 % (13/94) of the samples did not show seroconversion in any of the four antigen-based assays. In a double-blinded head-to-head comparison, ST based IgG ELISA displayed a better sensitivity (87.5 %, 95 % CI: 76.4-93.8 %) than the EUROIMMUN IgG ELISA (67.9 %, 95 % CI: 54.8-78.6 %). Further, in ST-based assays, we found 48 % and 50 % seroconversion in the first six days (from DOS) for IgG and IgA antibodies, respectively, which increased to 84 % (IgG) and 85 % (IgA) for samples collected ≥22 days from DOS.

conclusionsComparison of spike antigens demonstrates that spike trimer protein is a superior option as an ELISA antigen for COVID-19 serology.

Indexed as

Antibodies, ViralAntigens, ViralCOVID-19COVID-19 Serological TestingEnzyme-Linked Immunosorbent AssayHumansImmunoglobulin AImmunoglobulin GSARS-CoV-2Sensitivity and SpecificitySeroconversionSpike Glycoprotein, CoronavirusAntibodies, ViralAntigens, ViralImmunoglobulin AImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2SARS-CoV-2SerologySpike trimer ELISA

Identifiers

PMID34197839
PMCPMC8239204
OpenAlexW3174675651

What OpenQuestion holds

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Registered trials

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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.