Evidence map›Paper›PMID 36186648›Full record

ArticleFrontiers in pediatrics2022

Immune and pathophysiologic profiling of antenatal coronavirus disease 2019 in the GIFT cohort: A Singaporean case-control study.

Yue Gu, Jia Ming Low, Jolene Su Yi Tan, Melissa Shu Feng Ng, Lisa F P Ng, Bhuvaneshwari Shunmuganathan, Rashi Gupta, Paul A MacAry, Zubair Amin, Le Ye Lee and 4 more

Registry-linked trialAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04802278 (Gestational Immunity for Transfer), which is not on this map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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.

NCT04802278 unknown statusnot on this map

Gestational Immunity for Transfer

TypeobservationalSponsorNational University Hospital, SingaporeRan2020 to 2021Enrolled120ConditionsCovid19, Breastfeeding, Vaccine Exposure Via Breast MilkArmsCOVID-19 vaccine
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

14 authors.

Yue GuAntibody Engineering Programme, Life Sciences Institute, National University of Singapore, Singapore, Singapore.
Jia Ming LowDepartment of Neonatology, Khoo Teck Puat-National University Children's Medical Institute, National University Health System, Singapore, Singapore.
Jolene Su Yi TanDuke-NUS Medical School, Singapore, Singapore.
Melissa Shu Feng NgSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Lisa F P NgInfectious Diseases Labs, Agency for Science, Technology and Research, Singapore, Singapore.
Bhuvaneshwari ShunmuganathanAntibody Engineering Programme, Life Sciences Institute, National University of Singapore, Singapore, Singapore.
Rashi GuptaAntibody Engineering Programme, Life Sciences Institute, National University of Singapore, Singapore, Singapore.
Paul A MacAryAntibody Engineering Programme, Life Sciences Institute, National University of Singapore, Singapore, Singapore.
Zubair AminDepartment of Neonatology, Khoo Teck Puat-National University Children's Medical Institute, National University Health System, Singapore, Singapore.
Le Ye LeeDepartment of Neonatology, Khoo Teck Puat-National University Children's Medical Institute, National University Health System, Singapore, Singapore.
Derrick LianDepartment of Pathology, National University Hospital, Singapore, Singapore.
Lynette Pei-Chi ShekDepartment of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Youjia ZhongDepartment of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Liang Wei WangSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 can be severe in pregnant women, and have adverse consequences for the subsequent infant. We profiled the post-infectious immune responses in maternal and child blood as well as breast milk in terms of antibody and cytokine expression and performed histopathological studies on placentae obtained from mothers convalescent from antenatal COVID-19. Seventeen mother-child dyads (8 cases of antenatal COVID-19 and 9 healthy unrelated controls; 34 individuals in total) were recruited to the Gestational Immunity For Transfer (GIFT) study. Maternal and infant blood, and breast milk samples were collected over the first year of life. All samples were analyzed for IgG and IgA against whole SARS-CoV-2 spike protein, the spike receptor-binding domain (RBD), and previously reported immunodominant epitopes, as well as cytokine levels. The placentae were examined microscopically. The study is registered at clinicaltrials.gov under the identifier NCT04802278. We found high levels of virus-specific IgG in convalescent mothers and similarly elevated titers in newborn children. Thus, antenatal SARS-CoV-2 infection led to high plasma titers of virus-specific antibodies in infants postnatally. However, this waned within 3-6 months of life. Virus neutralization by plasma was not uniformly achieved, and the presence of antibodies targeting known immunodominant epitopes did not assure neutralization. Virus-specific IgA levels were variable among convalescent individuals' sera and breast milk. Antibody transfer ratios and the decay of transplacentally transferred virus-specific antibodies in neonatal circulation resembled that for other pathogens. Convalescent mothers showed signs of chronic inflammation marked by persistently elevated IL17RA levels in their blood. Four placentae presented signs of acute inflammation, particularly in the subchorionic region, marked by neutrophil infiltration even though > 50 days had elapsed between virus clearance and delivery. Administration of a single dose of BNT162b2 mRNA vaccine to mothers convalescent from antenatal COVID-19 increased virus-specific IgG and IgA titers in breast milk, highlighting the importance of receiving the vaccine even after natural infection with the added benefit of enhanced passive immunity.

Indexed as

antenatal COVID-19breast milk antibodiesGIFTplacental inflammationSARS-CoV-2transplacental antibody transfer

Identifiers

PMID36186648
PMCPMC9521552

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Registered trials

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.