Evidence map›Paper›PMID 36434068›Full record

ArticleNature communications2022

Comparison of antibody responses to SARS-CoV-2 variants in Australian children.

Zheng Quan Toh, Nadia Mazarakis, Jill Nguyen, Rachel A Higgins, Jeremy Anderson, Lien Anh Ha Do, David P Burgner, Nigel Curtis, Andrew C Steer, Kim Mulholland and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 23 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

13 authors at 3 institutions in 2 countries.

Zheng Quan Toh *Infection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.ORCID 0000-0002-0282-5837
Nadia Mazarakis *Infection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.ORCID 0000-0001-7681-2775
Jill NguyenInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Rachel A HigginsInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Jeremy AndersonInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Lien Anh Ha DoInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.ORCID 0000-0002-2401-8980
David P BurgnerInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.ORCID 0000-0002-8304-4302
Nigel CurtisInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Andrew C SteerInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Kim MulhollandInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Nigel W CrawfordInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Shidan TosifInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Paul V LicciardiInfection and Immunity, Murdoch Children's Research Institute, Parkville, VIC, Australia. paul.licciardi@mcri.edu.au.ORCID 0000-0001-6086-6285
Royal Children's Hospital · AUThe University of Melbourne · AUMurdoch Children's Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is limited understanding of antibody responses in children across different SARS-CoV-2 variants. As part of an ongoing household cohort study, we assessed the antibody response among unvaccinated children infected with Wuhan, Delta, or Omicron variants, as well as vaccinated children with breakthrough Omicron infection, using a SARS-CoV-2 S1-specific IgG assay and surrogate virus neutralization test (% inhibition). Most children infected with Delta (100%, 35/35) or Omicron (81.3%, 13/16) variants seroconverted by one month following infection. In contrast, 37.5% (21/56) children infected with Wuhan seroconverted, as previously reported. However, Omicron-infected children (geometric mean concentration 46.4 binding antibody units/ml; % inhibition = 16.3%) mounted a significantly lower antibody response than Delta (435.5 binding antibody untis/mL, % inhibition = 76.9%) or Wuhan (359.0 binding antibody units/mL, % inhibition = 74.0%). Vaccinated children with breakthrough Omicron infection mounted the highest antibody response (2856 binding antibody units/mL, % inhibition = 96.5%). Our findings suggest that despite a high seropositivity rate, Omicron infection in children results in lower antibody levels and function compared with Wuhan or Delta infection or with vaccinated children with breakthrough Omicron infection. Our data have important implications for public health measures and vaccination strategies to protect children.

Indexed as

COVID-19SARS-CoV-2Antibodies, ViralAntibody FormationAustraliaChildCohort StudiesHumansImmunoglobulin GAntibodies, ViralImmunoglobulin G

Identifiers

PMID36434068
PMCPMC9700848
OpenAlexW4309944431

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.