Evidence map›Paper›PMID 41080566›Full record

ArticleFrontiers in immunology2025

Autoantibody production in pregnancy: relationship with mRNA BNT162b2 immunization, active COVID-19, and pre-eclampsia.

Mauro César da Silva, George Tadeu Nunes Diniz, Maria Júlia da Silva Correia, Neila Caroline Henrique da Silva, Camila Rodrigues de Melo Barbosa, Ana Laura Carneiro Gomes Ferreira, Maria Inês Bezerra de Melo, Jurandy Júnior Ferraz de Magalhães, Eduardo Antônio Donadi, Ariani Impieri Souza and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. 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

11 authors.

Mauro César da SilvaLaboratory of Immunogenetics, Department of Immunology, Aggeu Magalhães Institute, Oswaldo Cruz Foundation, Recife, Brazil.
George Tadeu Nunes DinizLaboratory of Computational Methods, Aggeu Magalhães Institute, Recife, Brazil.
Maria Júlia da Silva CorreiaLaboratory of Immunogenetics, Department of Immunology, Aggeu Magalhães Institute, Oswaldo Cruz Foundation, Recife, Brazil.
Neila Caroline Henrique da SilvaLaboratory of Immunogenetics, Department of Immunology, Aggeu Magalhães Institute, Oswaldo Cruz Foundation, Recife, Brazil.
Camila Rodrigues de Melo BarbosaClinical Hospital, Federal University of Pernambuco, Recife, Brazil.
Ana Laura Carneiro Gomes FerreiraWomen Health Research Group of Instituto de Medicina Integral Prof. Fernando Figueira, Recife, Brazil.
Maria Inês Bezerra de MeloFaculdade Pernambucana de Saúde (FPS), Instituto de Medicina Integral Prof. Fernando Figueira (IMIP), Recife, Brazil.
Jurandy Júnior Ferraz de MagalhãesCentral Laboratory of Pernambuco, State Secretary of Health, Recife, Brazil.
Eduardo Antônio DonadiClinical Immunology Division, Department of Medicine, Ribeirão Preto Medical School, University of São Paulo (USP), Ribeirão Preto, Brazil.
Ariani Impieri SouzaWomen Health Research Group of Instituto de Medicina Integral Prof. Fernando Figueira, Recife, Brazil.
Norma Lucena-SilvaLaboratory of Immunogenetics, Department of Immunology, Aggeu Magalhães Institute, Oswaldo Cruz Foundation, Recife, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Starting June 2021, in Brazil, the COVID-19 vaccination campaign prioritized pregnant and postpartum women to use the mRNA-based BNT162b2 (Comirnaty) vaccine, the preferred choice due to its safety profile. Although mRNA vaccines are generally safe, concerns about potential autoimmune side effects have arisen. This study aimed to assess the frequency of autoantibody production among pregnant women vaccinated with BNT162b2 compared to unvaccinated groups with active COVID-19, pre-eclampsia, and healthy control women. We studied 273 pregnant women aged 18-48 years, stratified into four groups: healthy vaccinated, healthy unvaccinated, COVID-19 positive, and pre-eclampsia. An additional control group comprised 47 healthy, non-pregnant women. Autoantibodies were detected using the HEp-2 kit (EUROIMMUN, Lübeck, SH). Statistical analysis revealed that vaccinated pregnant women exhibited a significantly lower frequency of autoantibody production compared to their unvaccinated counterparts. No significant differences in autoantibody patterns were observed between vaccinated pregnant women and the control group. Notably, control group was associated with a higher frequency of specific autoantibody patterns, including AC-4 and AC-24. These findings suggest that BNT162b2 vaccination does not increase the risk of autoimmune responses in pregnant women, contrary to some concerns. The lower frequency of autoantibody observed in vaccinated individuals may reflect beneficial immunological mechanisms, such as immune modulation and reduced viral load. Further studies are needed to explore the relationship between autoantibody production and pregnancy-related autoimmune diseases.

Indexed as

AutoantibodiesBNT162 VaccineCOVID-19COVID-19 VaccinesPre-EclampsiaPregnancy Complications, InfectiousSARS-CoV-2AdolescentAdultAntibodies, ViralBrazilFemaleHumansMiddle AgedPregnancyVaccinationAntibodies, ViralAutoantibodiesBNT162 VaccineCOVID-19 VaccinesautoantibodiesBNT162b2COVID-19pre-eclampsiapregnancy

Identifiers

PMID41080566
PMCPMC12507805

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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.