Evidence map›Paper›PMID 38499828›Full record

ArticleInfection2024

Natural and hybrid immunity after SARS-CoV-2 infection in children and adolescents.

T Rothoeft, C Maier, A Talarico, A Hoffmann, A Schlegtendal, B Lange, A Petersmann, R Denz, N Timmesfeld, N Toepfner and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Infection, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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  5. Review
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 at 6 institutions in 1 country.

T RothoeftUniversity Hospital of Pediatrics and Adolescent Medicine, St. Josef-Hospital, Ruhr-University, Bochum, Germany. tobias.rothoeft@rub.de.
C MaierUniversity Hospital of Pediatrics and Adolescent Medicine, St. Josef-Hospital, Ruhr-University, Bochum, Germany.
A TalaricoUniversity Hospital of Pediatrics and Adolescent Medicine, St. Josef-Hospital, Ruhr-University, Bochum, Germany.
A HoffmannUniversity Hospital of Pediatrics and Adolescent Medicine, St. Josef-Hospital, Ruhr-University, Bochum, Germany.
A SchlegtendalUniversity Hospital of Pediatrics and Adolescent Medicine, St. Josef-Hospital, Ruhr-University, Bochum, Germany.
B LangeDepartment of Epidemiology, Helmholtz Centre for Infection Research, Brunswick, Germany.
A PetersmannUniversity Institute of Clinical Chemistry and Laboratory Medicine, University Medicine Oldenburg, Oldenburg, Germany.
R DenzDepartment of Medical Informatics, Biometry and Epidemiology, Ruhr-University Bochum, Bochum, Germany.
N TimmesfeldDepartment of Medical Informatics, Biometry and Epidemiology, Ruhr-University Bochum, Bochum, Germany.
N ToepfnerDepartment of Pediatrics, Faculty of Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
E Vidal-BlancoDepartment of Molecular and Medical Virology, Ruhr University Bochum, Bochum, Germany.
S PfaenderDepartment of Molecular and Medical Virology, Ruhr University Bochum, Bochum, Germany.
T LückeUniversity Hospital of Pediatrics and Adolescent Medicine, St. Josef-Hospital, Ruhr-University, Bochum, Germany.
F BrinkmannUniversity Hospital of Pediatrics and Adolescent Medicine, St. Josef-Hospital, Ruhr-University, Bochum, Germany.
Ruhr University Bochum · DESt. Josef-Hospital · DEZimmer Biomet (Germany) · DEHelmholtz Centre for Infection Research · DEUniversitätsmedizin Greifswald · DEUniversity Hospital Carl Gustav Carus · DE

Funding

Bundesministerium für Bildung und Forschung 01KI20173 (Corkid)Bundesministerium für Bildung und Forschung 01KX2121 (Immunebridge)
6 · The paper itself

Abstract

purposeIn contrast to adults, immune protection against SARS-CoV-2 in children and adolescents with natural or hybrid immunity is still poorly understood. The aim of this study was to analyze different immune compartments in different age groups and whether humoral immune reactions correlate with a cellular immune response.

methods72 children and adolescents with a preceding SARS-CoV-2 infection were recruited. 37 were vaccinated with an RNA vaccine (BNT162b2). Humoral immunity was analyzed 3-26 months (median 10 months) after infection by measuring Spike protein (S), nucleocapsid (NCP), and neutralizing antibodies (nAB). Cellular immunity was analyzed using a SARS-CoV-2-specific interferon-γ release assay (IGRA).

resultsAll children and adolescents had S antibodies; titers were higher in those with hybrid immunity (14,900 BAU/ml vs. 2118 BAU/ml). NCP antibodies were detectable in > 90%. Neutralizing antibodies (nAB) were more frequently detected (90%) with higher titers (1914 RLU) in adolescents with hybrid immunity than in children with natural immunity (62.5%, 476 RLU). Children with natural immunity were less likely to have reactive IGRAs (43.8%) than adolescents with hybrid immunity (85%). The amount of interferon-γ released by T cells was comparable in natural and hybrid immunity.

conclusionSpike antibodies are the most reliable markers to monitor an immune reaction against SARS-CoV-2. High antibody titers of spike antibodies and nAB correlated with cellular immunity, a phenomenon found only in adolescents with hybrid immunity. Hybrid immunity is associated with markedly higher antibody titers and a higher probability of a cellular immune response than a natural immunity.

Indexed as

Antibodies, NeutralizingAntibodies, ViralCOVID-19Immunity, CellularImmunity, HumoralSARS-CoV-2Spike Glycoprotein, CoronavirusAdolescentChildChild, PreschoolCoronavirus Nucleocapsid ProteinsCOVID-19 VaccinesFemaleHumansImmunity, InnateMaleAntibodies, NeutralizingAntibodies, ViralCoronavirus Nucleocapsid ProteinsCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2AntibodyChildrenConvalescentCOVID-19ImmunitySARS-CoV-2T cellVaccination

Identifiers

PMID38499828
PMCPMC11288991
OpenAlexW4392906035

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.