Evidence map›Paper›PMID 35788676›Full record

ArticleScientific reports2022

Development of an in-house quantitative ELISA for the evaluation of different Covid-19 vaccines in humans.

Mariem Gdoura, Fatma Ben Ghaloum, Meriem Ben Hamida, Wafa Chamsa, Henda Triki, Chokri Bahloul

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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 12 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

6 authors at 3 institutions in 1 country.

Mariem GdouraLaboratory of Clinical Virology, Institut Pasteur de Tunis, Tunis, Tunisia.
Fatma Ben GhaloumVaccinologie et Développement Biotechnologique, LR11IPT01 Microbiologie Moléculaire, Institut Pasteur de Tunis, Université de Tunis El Manar, 13, Place Pasteur, BP 74, 1002, Tunis-Belvedere, Tunisia.
Meriem Ben HamidaLaboratory of Clinical Virology, Institut Pasteur de Tunis, Tunis, Tunisia.
Wafa ChamsaLaboratory of Clinical Virology, Institut Pasteur de Tunis, Tunis, Tunisia.
Henda TrikiLaboratory of Clinical Virology, Institut Pasteur de Tunis, Tunis, Tunisia.
Chokri BahloulVaccinologie et Développement Biotechnologique, LR11IPT01 Microbiologie Moléculaire, Institut Pasteur de Tunis, Université de Tunis El Manar, 13, Place Pasteur, BP 74, 1002, Tunis-Belvedere, Tunisia. chokri.bahloul@pasteur.rns.tn.
Institut Pasteur de Tunis · TNTunis University · TNUniversity of Monastir · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reliable serological assays are needed to understand the real impact of COVID-19. In order to compare the efficiency of different COVID-19 vaccines used in the National Vaccination Program in Tunisia, we have developed a quantitative in-house ELISA. The ELISA is based on the ectodomain of the SARS-CoV-2 Spike Baculovirus recombinant protein. We used a panel of 145 COVID-19 RT-PCR positive serum samples and 116 pre-pandemic serum samples as a negative panel. The validation was carried out by comparison to four commercial techniques (Vidas SARS-CoV-2 IgG anti-RBD Biomérieux, Elecsys Anti-Nucleocapsid of SARS-CoV-2 Roche, cPass GenScript and the quantitative Elecsys Anti-RBD of SARS-CoV-2, Roche). For the evaluation of the National Vaccination campaign, we have included 115 recipients who received one of the approved vaccines. The qualitative performances of the developed ELISA gave 96% sensitivity, 97.5% specificity and 0.968 accuracy. For the evaluation of the different brand of vaccines in recipients not previously infected with SARS-CoV-2, it seems that mRNA vaccine of Pfizer/BioNTech has shown a higher efficacy compared to inactivated virus vaccines. COVID-19 convalescent individuals have generated poor antibody responses. Nevertheless, when they are vaccinated with any brand of the COVID-19 vaccines, many of them mounted an exponential increase of the induced immune responses, qualified as a "hybrid vigor immunity". Our developed in-house ELISA seems to be very efficient in evaluating the effectiveness of anti-COVID-19 vaccination. Platforms based on mRNA vaccine are better performing than those based on inactivated virus.

Indexed as

COVID-19Viral VaccinesCOVID-19 VaccinesEnzyme-Linked Immunosorbent AssayHumansmRNA VaccinesSARS-CoV-2Vaccines, InactivatedVaccines, SyntheticCOVID-19 VaccinesmRNA VaccinesVaccines, InactivatedVaccines, SyntheticViral Vaccines

Identifiers

PMID35788676
PMCPMC9252535
OpenAlexW4283794804

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.