Evidence map›Paper›PMID 39081316›Full record

ArticleFrontiers in immunology2024

The seroconversion history to SARS-CoV-2 in Indigenous people from Brazil - the interplay between exposure, vaccination, and tuberculosis.

Alice Nagai, Renan Barbosa Lemes, José Geraldo Mill, Alexandre Costa Pereira, Rafael Elias Marques, Tábita Hünemeier

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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.

Alice NagaiLaboratory of Pathogen Manipulation, Brazilian Biosciences National Laboratory (LNBio), Department of Virology, CNPEM (Brazilian Center for Research in Energy and Materials), Campinas, Brazil.
Renan Barbosa LemesHuman Population Genomics Laboratory, Biosciences Institute, Department of Genetics and Evolutionary Biology, University of São Paulo, São Paulo, Brazil.
José Geraldo MillHealth Sciences Center, Department of Physiological Sciences, Federal University of Espírito Santo, Vitória, Brazil.
Alexandre Costa PereiraLaboratory of Genetics and Molecular Cardiology, Instituto do Coração, Hospital das Clínicas, University of São Paulo, São Paulo, Brazil.
Rafael Elias MarquesLaboratory of Pathogen Manipulation, Brazilian Biosciences National Laboratory (LNBio), Department of Virology, CNPEM (Brazilian Center for Research in Energy and Materials), Campinas, Brazil.
Tábita HünemeierHuman Population Genomics Laboratory, Biosciences Institute, Department of Genetics and Evolutionary Biology, University of São Paulo, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic caused a significant loss of human lives and a worldwide decline in quality of life. Although our understanding of the pandemic has improved significantly since the beginning, the natural history of COVID-19 and its impacts on under-represented populations, such as Indigenous people from America, remain largely unknown. We performed a retrospective serological survey with two Brazilian Indigenous populations (n=624), Tupiniquim and Guarani-Mbyá. Samples were collected between September 2020 and July 2021: a period comprising the dissemination of SARS-CoV-2 variants and the beginning of COVID-19 vaccination in Brazil. Seroconversions against S and N antigens were assessed using three different commercially available ELISA kits. Samples were also used to assess the prevalence of tuberculosis (TB) in the same population (n=529). Seroconversion against SARS-CoV-2 antigens was considered positive if at least one of the three ELISA kits detected levels of specific antibodies above the threshold specified by the manufacturer. In this sense, we report 56.0% (n=349/623) of seroconverted individuals. Relative seroconversion peaked after introduction of the Coronavac vaccine in February 2021. Vaccination increased the production of anti-S IgG from 3.9% to 48.6%. Our results also indicated that 11.0% (n=46/417) of all individuals were positive for TB. Seroconversion to SARS-CoV-2 was similar between individuals with positive tuberculosis test results to those with negative test results. Most vaccinated individuals seroconverted to SARS-CoV-2, indicating that Coronavac may be as protective in individuals from these indigenous groups as observed in the general Brazilian population. COVID-19 severity was minimal regardless of incomplete vaccine coverage, suggesting that vaccination may not be the only factor protecting individuals from severe COVID-19. Tuberculosis is highly prevalent and not associated with increased seroconversion to SARS-CoV-2.

Indexed as

Antibodies, ViralCOVID-19SARS-CoV-2SeroconversionTuberculosisVaccinationAdolescentAdultAgedBrazilChildCOVID-19 VaccinesFemaleHumansIndigenous PeoplesMaleAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, CoronavirusBraziliansCOVID-19humoral responseIndigenoustuberculosisvaccination

Identifiers

PMID39081316
PMCPMC11286483

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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.