Evidence map›Paper›PMID 37898587›Full record

ArticleInfection2024

IgG antibody levels against the SARS-CoV-2 spike protein in mother-child dyads after COVID-19 vaccination.

María José Muñoz-Gómez, María Martin-Vicente, Sara Vigil-Vazquez, Itziar Carrasco, Alicia Hernanz Lobo, Vicente Mas, Mónica Vázquez, Angela Manzanares, Olga Cano, Clara Zamora and 8 more

Abstract read
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In one paragraph

Article in Infection, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 23% of its field
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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 at 5 institutions in 1 country.

María José Muñoz-Gómez *Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
María Martin-Vicente *Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
Sara Vigil-Vazquez *Sevicio de Neonatología, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Itziar CarrascoSevicio de Neonatología, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Alicia Hernanz LoboCentro de Investigación Biomédica en Red en Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain.
Vicente MasUnidad de Biología Viral, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Madrid, Spain.
Mónica VázquezUnidad de Biología Viral, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Madrid, Spain.
Angela ManzanaresServicio de Pediatría, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Olga CanoUnidad de Biología Viral, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Madrid, Spain.
Clara ZamoraServicio de Obstetricia y Ginecología, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Roberto AlonsoDepartamento de Microbiología Clínica y Enfermedades Infecciosas, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Daniel Sepulveda-CrespoUnidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
Laura Tarancon-DiezLaboratorio de InmunoBiología Molecular, Sección de Inmunología. Hospital General Universitario Gregorio Marañón, Madrid, Spain.
María Ángeles Muñoz-FernándezLaboratorio de InmunoBiología Molecular, Sección de Inmunología. Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Mar Muñoz-ChapuliServicio de Obstetricia y Ginecología, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Salvador Resino *Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain. sresino@isciii.es.
Maria Luisa Navarro *Centro de Investigación Biomédica en Red en Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain.
Isidoro Martinez *Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain. imago@isciii.es.
Hospital General Universitario Gregorio Marañón · ESInstituto de Salud Carlos III · ESCentro Nacional de Microbiologia · ESCentro de Investigación Biomédica en Red · ESUniversidad Complutense de Madrid · ES

Funding

Centro de Investigación Biomédica en Red de Enfermedades Infecciosas CB21/13/00044Centro de Investigación Biomédica en Red de Enfermedades Infecciosas CB21/13/00077Centro de Investigación Biomédica en Red en Bioingeniería, Biomateriales y Nanomedicina CB22/01/00041
6 · The paper itself

Abstract

purposeWe aimed to assess IgG antibodies against the SARS-CoV-2 spike protein (anti-SARS-CoV-2 S IgG) in vaccinated mothers and their infants at delivery and 2-3 months of age.

methodsWe conducted a prospective study on mothers who received at least one dose of the COVID-19 vaccine (Pfizer-BNT162b2, Moderna mRNA-1273, or Oxford-AstraZeneca ChAdOx1-S) during pregnancy and on their infants. The baseline was at the time of delivery (n = 93), and the end of follow-up was 2 to 3 months post-partum (n = 53). Serum anti-SARS-CoV-2 S IgG titers and ACE2 binding inhibition levels were quantified by immunoassays.

resultsMothers and infants had high anti-SARS-CoV-2 S IgG titers against the B.1 lineage at birth. However, while antibody titers were maintained at 2-3 months post-partum in mothers, they decreased significantly in infants (p < 0.001). Positive and significant correlations were found between anti-SARS-CoV-2 S IgG titers and ACE2-binding inhibition levels in mothers and infants at birth and 2-3 months post-partum (r > 0.8, p < 0.001). Anti-S antibodies were also quantified for the Omicron variant at 2-3 months post-partum. The antibody titers against Omicron were significantly lower in mothers and infants than those against B.1 (p < 0.001). Again, a positive correlation was observed for Omicron between IgG titers and ACE2-binding inhibition both in mothers (r = 0.818, p < 0.001) and infants (r = 0.386, p < 0.005). Previous SARS-CoV-2 infection and COVID-19 vaccination near delivery positively impacted anti-SARS-CoV-2 S IgG levels.

conclusionsCOVID-19 mRNA vaccines induce high anti-SARS-CoV-2 S titers in pregnant women, which can inhibit the binding of ACE2 to protein S and are efficiently transferred to the fetus. However, there was a rapid decrease in antibody levels at 2 to 3 months post-partum, particularly in infants.

Indexed as

Antibodies, ViralCOVID-19COVID-19 VaccinesImmunoglobulin GSARS-CoV-2Spike Glycoprotein, Coronavirus2019-nCoV Vaccine mRNA-1273AdultBNT162 VaccineChAdOx1 nCoV-19FemaleHumansInfantInfant, NewbornMalePregnancy2019-nCoV Vaccine mRNA-1273Antibodies, ViralBNT162 VaccineChAdOx1 nCoV-19COVID-19 VaccinesImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2AntibodyInfantPregnantSARS-CoV-2Spike glycoproteinVaccine

Identifiers

PMID37898587
OpenAlexW4388000119

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.