Evidence map›Paper›PMID 42036989›Full record

ArticleImmunity, inflammation and disease2026

Performance of Three Commercial Rapid Diagnostic Tests for Detection of IgM and IgG Antibodies Against SARS-CoV-2.

Moyra Machado Portilho, Stephane Fraga de Oliveira Tosta, Maysa Pellizzaro, Rosângela Oliveira Dos Anjos, Elaine Carvalho de Oliveira, Pamela Dos Santos Nascimento de Santana, Patrícia Sousa Dos Santos Moreira, Leile Camila Jacob-Nascimento, Mirela Maisa da Silva Souza, Deborah Bittencourt Mothé and 4 more

Abstract read
In one paragraph

Article in Immunity, inflammation and disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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5 · Who and what money

Authors and funding

14 authors.

Moyra Machado PortilhoInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Stephane Fraga de Oliveira TostaInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.ORCID https://orcid.org/0000-0001-5482-6789
Maysa PellizzaroInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Rosângela Oliveira Dos AnjosInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Elaine Carvalho de OliveiraInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Pamela Dos Santos Nascimento de SantanaInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Patrícia Sousa Dos Santos MoreiraInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Leile Camila Jacob-NascimentoInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Mirela Maisa da Silva SouzaSecretaria Municipal de Saúde de Salvador, Salvador, Brazil.
Deborah Bittencourt MothéInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Cláudia BrodskynInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Mitermayer Galvão ReisInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Cristiane Wanderley CardosoSecretaria Municipal de Saúde de Salvador, Salvador, Brazil.
Guilherme Sousa RibeiroInstituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 405308/2021-3Conselho Nacional de Desenvolvimento CientÍfico e TecnolÓgico 153384/2024-7Conselho Nacional de Desenvolvimento CientÍfico e TecnolÓgico 311365/2021-3Conselho Nacional de Desenvolvimento CientÍfico e TecnolÓgico 405308/2021-3Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorCoordenaÇÃo de AperfeiÇoamento de Pessoal de NÍvel Superior
6 · The paper itself

Abstract

backgroundDespite widespread vaccination, SARS-CoV-2 transmission continues, and serological testing remains relevant for selected diagnostic scenarios and population-based assessments of antibody responses. Rapid diagnostic tests (RDTs) for SARS-CoV-2 antibodies are attractive for field use and decentralized settings, but their diagnostic performance varies and requires independent evaluation. We assessed the performance of three commercially available lateral flow RDTs (PANBIO™ COVID-19 IgG/IgM Rapid Test Device, Bio-Manguinhos-Fiocruz TR COVID-19 (IgM-IgG), and Bio-Manguinhos-Fiocruz TR DPP® COVID-19 IgM/IgG) in Salvador, Brazil.

methodsUsing blind analyses, we evaluated 257 serum samples from RT-PCR-confirmed cases and 199 control samples from individuals with other febrile illnesses or healthy donors collected before and during the pandemic.

resultsOverall sensitivity for IgM or IgG detection was limited across all tests (52%-58%), while specificity was high for two assays (97%-98%) and lower for one (80%). Sensitivity peaked between 11 and 20 days after symptom onset (80%-91%) and declined thereafter. Among 75 vaccinated individuals without prior COVID-19, antibody positivity ranged from 39% to 55%.

conclusionThese findings indicate that the evaluated RDTs had high specificity but insufficient sensitivity for reliable clinical diagnosis or for assessing vaccination status in serological surveys. Our results support cautious use of these assays and highlight the need for more accurate and robust antibody-based rapid tests to strengthen immunological surveillance and public health preparedness in the post-pandemic period.

Indexed as

Antibodies, ViralCOVID-19COVID-19 Serological TestingImmunoglobulin GImmunoglobulin MSARS-CoV-2AdultAgedBrazilFemaleHumansMaleMiddle AgedRapid Diagnostic TestsSensitivity and SpecificityAntibodies, ViralImmunoglobulin GImmunoglobulin MCOVID‐19IgGIgMRapid testSARS‐COV‐2serological test

Identifiers

PMID42036989
PMCPMC13111801

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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.