Evidence map›Paper›PMID 36798400›Full record

ArticlebioRxiv : the preprint server for biology2023

Elevated binding and functional antibody responses to SARS-CoV-2 in infants versus mothers.

Caitlin I Stoddard, Kevin Sung, Zak A Yaffe, Haidyn Weight, Guillaume Beaudoin-Bussières, Jared Galloway, Soren Gantt, Judith Adhiambo, Emily R Begnel, Ednah Ojee and 7 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 4 countries.

Caitlin I StoddardHuman Biology Division, Fred Hutchinson Cancer Center.
Kevin SungPublic Health Sciences Division, Fred Hutchinson Cancer Center.
Zak A YaffeHuman Biology Division, Fred Hutchinson Cancer Center.
Haidyn WeightHuman Biology Division, Fred Hutchinson Cancer Center.
Guillaume Beaudoin-BussièresCentre de Recherche du CHUM, Université de Montréal.
Jared GallowayPublic Health Sciences Division, Fred Hutchinson Cancer Center.
Soren GanttDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal.
Judith AdhiamboDepartment of Pediatrics and Child Health, University of Nairobi.
Emily R BegnelDepartment of Global Health, University of Washington.
Ednah OjeeDepartment of Pediatrics and Child Health, University of Nairobi.
Jennifer SlykerDepartment of Global Health, University of Washington.
Dalton WamalwaDepartment of Pediatrics and Child Health, University of Nairobi.
John KinuthiaDepartment of Global Health, University of Washington.
Andrés FinziCentre de Recherche du CHUM, Université de Montréal.
Frederick A MatsenPublic Health Sciences Division, Fred Hutchinson Cancer Center.
Dara A LehmanHuman Biology Division, Fred Hutchinson Cancer Center.
Julie OverbaughHuman Biology Division, Fred Hutchinson Cancer Center.
Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAUniversity of Nairobi · KEUniversity of Washington · USCentre Hospitalier de l’Université de Montréal · CACentre Hospitalier Universitaire Sainte-Justine · CA

Funding

Comprehensive profiling of SARS-CoV-2 antibody responses and escape pathwaysR01AI138709 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI OVERBAUGH, JULIE M. · 2018 to 2022
$5.0M
Maternal-infant Virome Transmission: the role of HIV and Antiretroviral TherapyR01HD092311 · NICHD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEHMAN, DARA ANN · 2017 to 2021
$3.9M
Blending deep learning with probabilistic mechanistic models to predict and understand the evolution and function of adaptive immune receptorsR01AI146028 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MATSEN, FREDERICK ALBERT · 2019 to 2024
$3.4M
High-Performance Compute Cluster for Comprehensive Cancer and Infectious Diseases ResearchS10OD028685 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BRADLEY, PHILIP · 2020 to 2020
$2.0M
The Virome and Microbiome in Health and BK Disease of Kidney Transplant PatientsR00DK107923 · NIDDK · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI LIM, EFREM · 2017 to 2019
$747k
Innate immune factors governing restriction of human coronavirusesK99AI171000 · NIAID · FRED HUTCHINSON CANCER CENTER · PI STODDARD, CAITLIN · 2022 to 2023
$257k
Studying the Contribution of Env-SpecificAntibodies to Mother to Child Transmission of HIV-1F30AI165112 · NIAID · UNIVERSITY OF WASHINGTON · PI YAFFE, ZACHARY A · 2021 to 2023
$141k
NIAID NIH HHS F30 AI165112NIAID NIH HHS K99 AI171000NIAID NIH HHS R01 AI138709NIAID NIH HHS R01 AI146028NICHD NIH HHS R01 HD092311NIDDK NIH HHS R00 DK107923NIH HHS S10 OD028685
6 · The paper itself

Abstract

Infant antibody responses to viral infection can differ from those in adults. However, data on the specificity and function of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibodies in infants, and direct comparisons between infants and adults are limited. We characterized antibody binding and functionality in convalescent plasma from postpartum women and their infants infected with SARS-CoV-2 from a vaccine-naïve prospective cohort in Nairobi, Kenya. Antibody titers against SARS-CoV-2 Spike, receptor binding domain and N-terminal domain, and Spike-expressing cell-surface staining levels were significantly higher in infants than in mothers. Plasma antibodies from mothers and infants bound to similar regions of the Spike S2 subunit, including the fusion peptide (FP) and stem helix-heptad repeat 2. However, infants displayed higher antibody levels and more consistent antibody escape pathways in the FP region compared to mothers. Finally, infants had significantly higher levels of antibody-dependent cellular cytotoxicity (ADCC), though, surprisingly, neutralization titers between infants and mothers were similar. These results suggest infants develop distinct SARS-CoV-2 binding and functional antibody repertoires and reveal age-related differences in humoral immunity to SARS-CoV-2 infection that could be relevant to protection and COVID-19 disease outcomes.

Identifiers

PMID36798400
PMCPMC9934573
OpenAlexW4319337123

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.