Evidence map›Paper›PMID 38241046›Full record

ArticleJAMA network open2024

Timing of Maternal COVID-19 Vaccine and Antibody Concentrations in Infants Born Preterm.

Alisa Kachikis, Mindy Pike, Linda O Eckert, Emma Roberts, Yael Frank, Amber L Young, Erin Goecker, Michael G Gravett, Alexander L Greninger, Janet A Englund

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Alisa KachikisDepartment of Obstetrics and Gynecology, University of Washington, Seattle.
Mindy PikeDepartment of Obstetrics and Gynecology, University of Washington, Seattle.
Linda O EckertDepartment of Obstetrics and Gynecology, University of Washington, Seattle.
Emma RobertsDepartment of Obstetrics and Gynecology, University of California, San Diego.
Yael FrankSchool of Medicine, Tel Aviv University, Tel Aviv, Israel.
Amber L YoungDepartment of Obstetrics and Gynecology, University of Washington, Seattle.
Erin GoeckerDepartment of Laboratory Medicine, University of Washington, Seattle.
Michael G GravettDepartment of Obstetrics and Gynecology, University of Washington, Seattle.
Alexander L GreningerDepartment of Laboratory Medicine, University of Washington, Seattle.
Janet A EnglundSeattle Children's Hospital Research Institute, Department of Pediatrics, University of Washington, Seattle.
University of Washington · USTel Aviv University · ILUniversity of California, San Diego · US

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
WOMEN'S REPRODUCTIVE HEALTH RESEARCH CAREER DEVELOPMENTK12HD001264 · NICHD · UNIVERSITY OF WASHINGTON · PI Barbara Ann Goff · 1998 to 2026
$8.6M
Protection of at-risk low birth weight infants against influenza via maternal antibodyK23AI153390 · NIAID · UNIVERSITY OF WASHINGTON · PI KACHIKIS, ALISA · 2021 to 2025
$942k
NCATS NIH HHS UL1 TR002319NIAID NIH HHS K23 AI153390NICHD NIH HHS K12 HD001264
6 · The paper itself

Abstract

Importance: COVID-19 vaccine-derived antibodies in pregnant people may protect infants from severe infection in the first 6 months of life via transplacental antibody transfer. Few data exist on maternally derived SARS-CoV-2 antibodies in preterm compared with full-term infants in association with vaccination timing. Objective: To compare SARS-CoV-2 anti-Spike (anti-S) antibody levels in preterm and full-term infants in the context of vaccine dose timing before delivery. Design, Setting, and Participants: This prospective cohort study enrolled pregnant individuals and collected paired maternal and cord blood samples at delivery at the University of Washington between February 1, 2021, and January 31, 2023. Participants who had received at least 2 doses of a messenger RNA COVID-19 vaccine before delivery and did not have a history of prior COVID-19 infection or detectable anti-SARS-CoV-2 nucleocapsid antibodies were included. Exposures: Timing of the last vaccine dose and preterm or full-term gestational age at delivery. Main Outcomes and Measures: Paired maternal and cord samples were tested for anti-S antibody, and linear regression was used to evaluate associations between preterm delivery and anti-S antibody levels. Covariates included timing of last dose, number of doses, insurance status, and immunosuppressing medications. Results: A total of 220 participants (median [IQR] age, 34 [32-37] years; 212 [96.4%] female) with 36 preterm and 184 full-term deliveries were studied. Before delivery, 121 persons received 2 vaccine doses and 99 persons received 3 or more vaccine doses. The geometric mean concentration of maternal anti-S antibodies was 674 (95% CI, 577-787) after 2 doses and 8159 (95% CI, 6636-10 032) after 3 or more doses (P < .001). The cord anti-S antibody geometric mean concentration was 1000 (95% CI, 874-1144) after 2 doses and 9992 (95% CI, 8381-11 914) after 3 or more doses (P < .001). After adjustment for vaccine timing and number of doses before delivery, no association was found between preterm delivery and cord anti-S antibody levels (β = 0.44; 95% CI, -0.06 to 0.94). Conclusions and Relevance: In this prospective cohort study of pregnant individuals with preterm and full-term deliveries, receipt of 3 or more compared with 2 doses of COVID-19 vaccine before delivery resulted in 10-fold higher cord anti-S antibody levels. Maternal antibody concentration appeared more important than delivery gestational age in determining cord anti-S antibody levels. The number of doses and timing considerations for COVID-19 vaccine in pregnancy should include individuals at risk for preterm delivery.

Indexed as

Cone-Rod DystrophiesCOVID-19Premature BirthAdultAntibodies, ViralCOVID-19 VaccinesFemaleHumansInfantInfant, NewbornMalePregnancyProspective StudiesSARS-CoV-2Antibodies, ViralCOVID-19 Vaccines

Identifiers

PMID38241046
PMCPMC10799259
OpenAlexW4391035392

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.