Evidence map›Paper›PMID 37615311›Full record

ArticleWomen's health (London, England)

Severe acute respiratory syndrome coronavirus 2 seroprevalence and longitudinal antibody response following natural infection in pregnancy: A prospective cohort study.

Alison L Drake, Jaclyn N Escudero, Morgan C Aurelio, Erica A Wetzler, Sascha R Ellington, Lauren B Zapata, Romeo R Galang, Margaret C Snead, Krissy Yamamoto, Carol C Salerno and 5 more

Open access · goldAbstract read
In one paragraph

Article in Women's health (London, England). 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
0.6field-weighted citation impact, top 29% 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, 2 citations in OpenAlex.

  1. Article
  2. 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

15 authors at 3 institutions in 1 country.

Alison L DrakeDepartment of Global Health, University of Washington, Seattle, WA, USA.
Jaclyn N EscuderoDepartment of Global Health, University of Washington, Seattle, WA, USA.
Morgan C AurelioDepartment of Global Health, University of Washington, Seattle, WA, USA.ORCID 0000-0001-8863-4697
Erica A WetzlerDepartment of Global Health, University of Washington, Seattle, WA, USA.
Sascha R EllingtonDivision of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Lauren B ZapataDivision of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, GA, USA.ORCID 0000-0002-6536-7124
Romeo R GalangDivision of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Margaret C SneadDivision of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, GA, USA.ORCID 0000-0002-5020-3311
Krissy YamamotoDepartment of Obstetrics & Gynecology, University of Washington, Seattle, WA, USA.
Carol C SalernoDepartment of Obstetrics & Gynecology, University of Washington, Seattle, WA, USA.
Barbra A RichardsonDepartment of Global Health, University of Washington, Seattle, WA, USA.
Alexander L GreningerDepartment of Laboratory Medicine & Pathology, University of Washington, Seattle, WA, USA.
Alisa B KachikisDepartment of Obstetrics & Gynecology, University of Washington, Seattle, WA, USA.
Janet A EnglundDepartment of Pediatrics, University of Washington, Seattle, WA, USA.
Sylvia M LaCourseDepartment of Global Health, University of Washington, Seattle, WA, USA.
University of Washington · USCenters for Disease Control and Prevention · USSeattle Children's Hospital · US

Funding

Protection of at-risk low birth weight infants against influenza via maternal antibodyK23AI153390 · NIAID · UNIVERSITY OF WASHINGTON · PI KACHIKIS, ALISA · 2021 to 2025
$942k
NIAID NIH HHS K23 AI153390
6 · The paper itself

Abstract

backgroundAntenatal care provides unique opportunities to assess severe acute respiratory syndrome coronavirus 2 seroprevalence and antibody response duration after natural infection detected during pregnancy; transplacental antibody transfer may inform peripartum and neonatal protection. We estimated seroprevalence and durability of antibodies from natural infection (anti-nucleocapsid immunoglobulin G) among pregnant people, and evaluated transplacental transfer efficiency. OBJECTIVE AND

designWe conducted a cross-sectional study to measure severe acute respiratory syndrome coronavirus 2 seroprevalence, and a prospective cohort study to longitudinally measure anti-nucleocapsid immunoglobulin G responses and transplacental transfer of maternally derived anti-nucleocapsid antibodies.

methodsWe screened pregnant people for the seroprevalence study between 9 December 2020 and 19 June 2021 for anti-nucleocapsid immunoglobulin G in Seattle, Washington. We enrolled anti-nucleocapsid immunoglobulin G positive people from the seroprevalence study or identified through medical records with positive reverse transcription polymerase chain reaction or antigen positive results in a prospective cohort between 9 December 2020 and 9 August 2022.

resultsIn the cross-sectional study (N = 1284), 5% (N = 65) tested severe acute respiratory syndrome coronavirus 2 anti-nucleocapsid immunoglobulin G positive, including 39 (60%) without prior positive reverse transcription polymerase chain reaction results and 42 (65%) without symptoms. In the prospective cohort study (N = 107 total; N = 65 from the seroprevalence study), 86 (N = 80%) had anti-nucleocapsid immunoglobulin G positive results during pregnancy. Among 63 participants with delivery samples and prior anti-nucleocapsid positive results, 29 (46%) were anti-nucleocapsid immunoglobulin G negative by delivery. Of 34 remaining anti-nucleocapsid immunoglobulin G positive at delivery with paired cord blood, 19 (56%) had efficient transplacental anti-nucleocapsid immunoglobulin G antibody transfer. Median time from first anti-nucleocapsid immunoglobulin G positive to below positive antibody threshold was 19 weeks and did not differ by prior positive reverse transcription polymerase chain reaction status.

conclusionsMaternally derived severe acute respiratory syndrome coronavirus 2 antibodies to natural infection may wane before delivery. Vaccines are recommended for pregnant persons to reduce severe illness and confer protection to infants.

Indexed as

COVID-19SARS-CoV-2Antibody FormationCross-Sectional StudiesFemaleHumansImmunoglobulin GInfantInfant, NewbornPregnancyProspective StudiesSeroepidemiologic StudiesImmunoglobulin Gantibodynatural infectionpregnancySARS-CoV-2seroprevalencetransplacental transfer

Identifiers

PMID37615311
PMCPMC10467162
OpenAlexW4386117243

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.