Evidence map›Paper›PMID 40664396›Full record

Observational studyClinical infectious diseases : an official publication of the Infectious Diseases Society of America2025

Antibody Response in Healthcare Workers During the SARS-CoV-2 Gamma Variant Outbreak in Manaus, Brazil.

Charlene Siza, Mateusz Plucinski, Fernanda C Lessa, Evelyn Campelo, Maria Clara Padoveze, Antonio R Vieira, Gemma Parra, Guilherme Araujo, Lucia Y I Nichiata, Luciana Silva-Flannery and 11 more

Abstract readObservational Study
In one paragraph

Observational study in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Charlene SizaCOVID-19 Response - International Task Force, Centers for Diseases Control and Prevention (CDC), Atlanta, Georgia, USA.ORCID 0000-0002-6704-9509
Mateusz PlucinskiCOVID-19 Response - International Task Force, Centers for Diseases Control and Prevention (CDC), Atlanta, Georgia, USA.ORCID 0000-0002-7322-4625
Fernanda C LessaCOVID-19 Response - International Task Force, Centers for Diseases Control and Prevention (CDC), Atlanta, Georgia, USA.
Evelyn CampeloFundação de Vigilância em Saúde do Estado do Amazonas, Manaus, Amazonas, Brazil.
Maria Clara PadovezeUniversidade de São Paulo, Escola de Enfermagem, São Paulo, Sao Paulo, Brazil.ORCID 0000-0002-1912-7293
Antonio R VieiraCOVID-19 Response - International Task Force, Centers for Diseases Control and Prevention (CDC), Atlanta, Georgia, USA.
Gemma ParraDivision of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Guilherme AraujoLaboratório Central do Amazonas (LACEN), Manaus, Amazonas, Brazil.
Lucia Y I NichiataUniversidade de São Paulo, Escola de Enfermagem, São Paulo, Sao Paulo, Brazil.ORCID 0000-0001-6515-4404
Luciana Silva-FlanneryCOVID-19 Response - International Task Force, Centers for Diseases Control and Prevention (CDC), Atlanta, Georgia, USA.ORCID 0000-0002-5762-8451
Kassia LimaHospital Pronto Socorro 28 de Agosto, Manaus, Amazonas, Brazil.ORCID 0000-0001-8952-5927
Aida Cristina TapajosHospital Pronto Socorro Platão Araújo, Manaus, Amazonas, Brazil.
Ariana VieiraHospital Pronto Socorro Platão Araújo, Manaus, Amazonas, Brazil.
Juliette MorganSouth America Regional Office, Centers for Disease Control and Prevention (CDC), Brasília, Federal District, Brazil.ORCID 0000-0002-9926-8669
Roberto J Freire EstevesSouth America Regional Office, Centers for Disease Control and Prevention (CDC), Brasília, Federal District, Brazil.
Barbara MarstonCOVID-19 Response - International Task Force, Centers for Diseases Control and Prevention (CDC), Atlanta, Georgia, USA.
Cristiano Fernandes da CostaConselho de Secretarias Municipais de Saúde do Amazonas, Manaus, Amazonas, Brazil.ORCID 0000-0002-7821-5752
Felipe G NavecaInstituto Leônidas e Maria Deane, Fiocruz, Amazonas, Brazil.ORCID 0000-0002-2888-1060
Tatyana C Amorim RamosFundação de Vigilância em Saúde do Estado do Amazonas, Manaus, Amazonas, Brazil.
Pritesh LalwaniInstituto Leônidas e Maria Deane, Fiocruz, Amazonas, Brazil.ORCID 0000-0003-2996-0446
Brazil Healthcare Personnel COVID-19 team

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to evaluate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-specific binding and neutralizing antibody responses in healthcare workers (HCWs) who received coronavirus disease 2019 (COVID-19) vaccines, with or without postvaccination infections.

methodsWe conducted a prospective, observational cohort study of HCW in 2 hospitals in Manaus, Brazil. From 31 March through 31 May 2021, HCWs had nasal swabs collected and questionnaires administered weekly for 4 visits. Nasal swabs were tested for SARS-CoV-2 by real-time reverse transcription polymerase chain reaction (rRT-PCR). Blood specimens were obtained at visits 1 and 4 unless the HCW was found to be infected. If infected, a blood specimen was collected on days 14 and 28 after symptom onset or date of positive specimen, if asymptomatic. COVID-19 vaccination cards, state immunization records, and self-reported history of previous SARS-CoV-2 infection were obtained. Fully vaccinated HCWs who tested SARS-CoV-2 rRT-PCR positive were classified as postvaccination infections.

resultsA total of 771 HCWs were enrolled, with 73.7% (568/771) fully vaccinated. Anti-SARS-CoV-2 S1 immunoglobulin G and neutralizing antibody levels showed steep decay within the first 50 days after COVID-19 vaccination. HCWs with prior SARS-CoV-2 infection had slower visible decay after 50 days compared with those without prior infection. We identified 12 postvaccination infections of 16 HCWs who were SARS-CoV-2 rRT-PCR+, including 4 who also reported previous infection. Those positive for SARS-CoV-2 had lower baseline neutralizing antibody levels against Gamma and Delta variants preinfection (median log10 titers [interquartile range]: Gamma, 1.5 [3]; Delta: 0 [0.25]) compared to those who remained rRT-PCR negative (median log10 titers [interquartile range]: Gamma, 3 [2]; Delta, 1 [2]).

conclusionsOur findings highlight the importance of routine antibody surveillance, targeted boosters, and hybrid immunity in low and middle income countries. Timely booster doses for HCWs and the development of new vaccines against emerging variants can help sustain immunity and prevent workforce shortages, strengthening healthcare resilience in resource-limited settings.

Indexed as

Antibodies, ViralAntibody FormationCOVID-19COVID-19 VaccinesHealth PersonnelSARS-CoV-2AdultAntibodies, NeutralizingBrazilDisease OutbreaksFemaleHumansMaleMiddle AgedProspective StudiesAntibodies, NeutralizingAntibodies, ViralCOVID-19 Vaccinesantibody responsesbreakthrough infectionsCOVID-19healthcare workersSARS-CoV-2

Identifiers

PMID40664396
PMCPMC12448572

What OpenQuestion holds

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LicenceCC BY
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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.