Evidence map›Paper›PMID 34124701›Full record

ArticleCell reports. Medicine2021

Young infants exhibit robust functional antibody responses and restrained IFN-γ production to SARS-CoV-2.

Anu Goenka, Alice Halliday, Michaela Gregorova, Emily Milodowski, Amy Thomas, Maia Kavanagh Williamson, Holly Baum, Elizabeth Oliver, Anna E Long, Lea Knezevic and 16 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Cell reports. Medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 35 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

26 authors at 7 institutions in 2 countries.

Anu GoenkaSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Alice HallidaySchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Michaela GregorovaSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Emily MilodowskiBristol Veterinary School, University of Bristol, Bristol, UK.
Amy ThomasBristol Veterinary School, University of Bristol, Bristol, UK.
Maia Kavanagh WilliamsonSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Holly BaumSchool of Chemistry, University of Bristol, Bristol, UK.
Elizabeth OliverSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Anna E LongDiabetes and Metabolism, Bristol Medical School, University of Bristol, Bristol, UK.
Lea KnezevicBristol Veterinary School, University of Bristol, Bristol, UK.
Alistair J K WilliamsDiabetes and Metabolism, Bristol Medical School, University of Bristol, Bristol, UK.
Vito LampasonaDiabetes Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Lorenzo PiemontiDiabetes Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Kapil GuptaSchool of Biochemistry, University of Bristol, Bristol, UK.
Natalie Di BartoloBristol Synthetic Biology Centre, University of Bristol, Bristol, UK.
Imre BergerBristol Synthetic Biology Centre, University of Bristol, Bristol, UK.
Ashley M ToyeBristol Synthetic Biology Centre, University of Bristol, Bristol, UK.
Barry VipondNational Infection Service, Public Health England South West, Southmead Hospital, Bristol, UK.
Peter MuirNational Infection Service, Public Health England South West, Southmead Hospital, Bristol, UK.
Jolanta BernatonieneDepartment of Paediatric Immunology and Infectious Diseases, Bristol Royal Hospital for Children, Bristol, UK.
Mick BaileyBristol Veterinary School, University of Bristol, Bristol, UK.
Kathleen M GillespieDiabetes and Metabolism, Bristol Medical School, University of Bristol, Bristol, UK.
Andrew D DavidsonSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Linda WooldridgeBristol Veterinary School, University of Bristol, Bristol, UK.
Laura RivinoSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Adam FinnSchool of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
University of Bristol · GBBristol Royal Hospital for Children · GBBristol Institute for Transfusion Sciences · GBIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto di Ricovero e Cura a Carattere Scientifico San RaffaelePublic Health England · GBSouthmead Hospital · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L01386X/1Medical Research Council MR/V027506/1Wellcome TrustWellcome Trust 106115/Z/14/ZWellcome Trust 204813/Z/16/Z
6 · The paper itself

Abstract

Severe COVID-19 appears rare in children. This is unexpected, especially in young infants, who are vulnerable to severe disease caused by other respiratory viruses. We evaluate convalescent immune responses in 4 infants under 3 months old with confirmed COVID-19 who presented with mild febrile illness, alongside their parents, and adult controls recovered from confirmed COVID-19. Although not statistically significant, compared to seropositive adults, infants have high serum levels of IgG and IgA to SARS-CoV-2 spike protein, with a corresponding functional ability to block SARS-CoV-2 cellular entry. Infants also exhibit robust saliva anti-spike IgG and IgA responses. Spike-specific IFN-γ production by infant peripheral blood mononuclear cells appears restrained, but the frequency of spike-specific IFN-γ- and/or TNF-α-producing T cells is comparable between infants and adults. On principal-component analysis, infant immune responses appear distinct from their parents. Robust functional antibody responses alongside restrained IFN-γ production may help protect infants from severe COVID-19.

Indexed as

Antibody FormationAdultCOVID-19FemaleHumansImmunoglobulin AImmunoglobulin GInfantInfant, NewbornInterferon-gammaLeukocytes, MononuclearMaleSpike Glycoprotein, CoronavirusYoung AdultImmunoglobulin AImmunoglobulin GInterferon-gammaSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2antibodyCOVID-19immunityinfantT cell

Identifiers

PMID34124701
PMCPMC8188298
OpenAlexW3166838531

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.