Evidence map›Paper›PMID 39061652›Full record

ArticleDiagnostics (Basel, Switzerland)2024

Comprehensive Study of the IBMP ELISA IgA/IgM/IgG COVID-19 Kit for SARS-CoV-2 Antibody Detection.

Sibelle Botogosque Mattar, Paola Alejandra Fiorani Celedon, Leonardo Maia Leony, Larissa de Carvalho Medrado Vasconcelos, Daniel Dias Sampaio, Fabricio Klerynton Marchini, Luis Gustavo Morello, Vanessa Hoysan Lin, Sandra Crestani, Aquiles Assunção Camelier and 8 more

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

18 authors.

Sibelle Botogosque MattarMolecular Biology Institute of Paraná (IBMP), Curitiba 81350-010, PR, Brazil.
Paola Alejandra Fiorani CeledonMolecular Biology Institute of Paraná (IBMP), Curitiba 81350-010, PR, Brazil.
Leonardo Maia LeonyInterdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation-Bahia (FIOCRUZ-BA), Salvador 402596-710, BA, Brazil.
Larissa de Carvalho Medrado VasconcelosInterdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation-Bahia (FIOCRUZ-BA), Salvador 402596-710, BA, Brazil.
Daniel Dias SampaioInterdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation-Bahia (FIOCRUZ-BA), Salvador 402596-710, BA, Brazil.
Fabricio Klerynton MarchiniMolecular Biology Institute of Paraná (IBMP), Curitiba 81350-010, PR, Brazil.
Luis Gustavo MorelloMolecular Biology Institute of Paraná (IBMP), Curitiba 81350-010, PR, Brazil.
Vanessa Hoysan LinMolecular Biology Institute of Paraná (IBMP), Curitiba 81350-010, PR, Brazil.
Sandra CrestaniMolecular Biology Institute of Paraná (IBMP), Curitiba 81350-010, PR, Brazil.
Aquiles Assunção CamelierAliança D'Or Hospital, Salvador 41920-180, BA, Brazil.ORCID 0000-0001-5410-5180
André Costa MeirelesAliança D'Or Hospital, Salvador 41920-180, BA, Brazil.ORCID 0000-0002-4974-0494
André Luiz Freitas de Oliveira JuniorAliança D'Or Hospital, Salvador 41920-180, BA, Brazil.
Antônio Carlos BandeiraAeroporto Hospital, Lauro de Freitas 42700-000, BA, Brazil.ORCID 0000-0002-7273-8376
Yasmin Santos Freitas MacedoLaboratory of Investigation in Global Health and Neglected Diseases, Gonçalo Moniz Institute, Oswaldo Cruz Foundation-Bahia (FIOCRUZ-BA), Salvador 402596-710, BA, Brazil.
Alan Oliveira DuarteLaboratory of Investigation in Global Health and Neglected Diseases, Gonçalo Moniz Institute, Oswaldo Cruz Foundation-Bahia (FIOCRUZ-BA), Salvador 402596-710, BA, Brazil.ORCID 0000-0003-3810-7332
Tycha Bianca Sabaini PavanInterdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation-Bahia (FIOCRUZ-BA), Salvador 402596-710, BA, Brazil.ORCID 0000-0001-5276-2099
Isadora Cristina de SiqueiraInterdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation-Bahia (FIOCRUZ-BA), Salvador 402596-710, BA, Brazil.ORCID 0000-0002-2520-4099
Fred Luciano Neves SantosInterdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation-Bahia (FIOCRUZ-BA), Salvador 402596-710, BA, Brazil.ORCID 0000-0002-3944-0818

Funding

Fundação para o Desenvolvimento Científico e Tecnológico em Saúde - Fiotec Av. Brasil, nº 4.036, Manguinhos CEP 21040-361 - Rio de Janeiro - RJ FIOTEC
6 · The paper itself

Abstract

COVID-19 laboratory diagnosis primarily relies on molecular tests, highly sensitive during early infection stages with high viral loads. As the disease progresses, sensitivity decreases, requiring antibody detection. Since the beginning of the pandemic, serological tests have been developed and made available in Brazil, but their diagnostic performance varies. This study evaluated the IBMP ELISA IgA/IgM/IgG COVID-19 kit performance in detecting SARS-CoV-2 antibodies. A total of 90 samples, including 64 from COVID-19 patients and 26 pre-pandemic donors, were assessed based on time post symptom onset (0-7, 8-14, and 15-21 days). The kit showed 61% sensitivity, 100% specificity, and 72% accuracy overall. Sensitivity varied with time, being 25%, 57%, and 96% for 0-7, 8-14, and 15-21 days, respectively. Similar variations were noted in other commercial tests. The Gold ELISA COVID-19 (IgG/IgM) had sensitivities of 31%, 71%, and 100%, while the Anti-SARS-CoV-2 NCP ELISA (IgG) and Anti-SARS-CoV-2 NCP ELISA (IgM) showed varying sensitivities. The IBMP ELISA kit displayed high diagnostic capability, especially as the disease progressed, complementing COVID-19 diagnosis. Reproducibility assessment revealed minimal systematic and analytical errors. In conclusion, the IBMP ELISA IgA/IgM/IgG COVID-19 kit is a robust tool for detecting anti-SARS-CoV-2 antibodies, increasing in efficacy over the disease course, and minimizing false negatives in RT-PCR COVID-19 diagnosis.

Indexed as

COVID-19immunodiagnosisSARS-CoV-2sensitivityspecificity

Identifiers

PMID39061652
PMCPMC11276192

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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.