Evidence map›Paper›PMID 36593041›Full record

ArticleIn vivo (Athens, Greece)

Age-related Differences in Immune Reactions to SARS-CoV-2 Spike and Nucleocapsid Antigens.

Patrick Morhart, Sven Kehl, Wolfgang Schuh, Katharina Hermes, Stefan Meltendorf, Antje Neubert, Michael Schneider, Monika Brunner-Weinzierl, Holm Schneider, Holger Lingel

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.7field-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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Age-Specific Cytokine Profiling in Children withJournal of inflammation research · 2025
    Article
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  5. Article
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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

10 authors at 3 institutions in 1 country.

Patrick MorhartDepartment of Pediatrics, University of Erlangen-Nürnberg, Erlangen, Germany; patrick.morhart@uk-erlangen.de.
Sven KehlDepartment of Obstetrics and Gynecology, University of Erlangen-Nürnberg, Erlangen, Germany.
Wolfgang SchuhDivision of Molecular Immunology, University of Erlangen-Nürnberg, Erlangen, Germany.
Katharina HermesHauner'sches Kinderspital, University of Munich, Munich, Germany.
Stefan MeltendorfDepartment of Experimental Pediatrics, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Antje NeubertDepartment of Pediatrics, University of Erlangen-Nürnberg, Erlangen, Germany.
Michael SchneiderDepartment of Obstetrics and Gynecology, University of Erlangen-Nürnberg, Erlangen, Germany.
Monika Brunner-WeinzierlDepartment of Experimental Pediatrics, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Holm SchneiderDepartment of Pediatrics, University of Erlangen-Nürnberg, Erlangen, Germany.
Holger LingelDepartment of Experimental Pediatrics, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEOtto-von-Guericke University Magdeburg · DEMünchen Klinik · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimThe manifestation and severity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections show a clear correlation to the age of a patient. The younger a person, the less likely the infection results in significant illness. To explore the immunological characteristics behind this phenomenon, we studied the course of SARS-CoV-2 infections in 11 households, including 8 children and 6 infants/neonates of women who got infected with SARS-CoV-2 during pregnancy. MATERIALS AND

methodsWe investigated the immune responses of peripheral blood mononuclear cells (PBMCs), umbilical cord blood mononuclear cells (UCBCs), and T cells against spike and nucleocapsid antigens of SARS-COV-2 by flow cytometry and cytokine secretion assays.

resultsUpon peptide stimulation, UCBC from neonates showed a strongly reduced IFN-γ production, as well as lower levels of IL-5, IL-13, and TNF-α alongside with decreased frequencies of surface CD137/PD-1 co-expressing CD4

conclusionThe increased severity of SARS-CoV-2 infections in adults could result from the strong cytokine production and lower potential to immunomodulate the excessive inflammation, while the limited IFN-γ production of responding T cells in infants/neonates and the additional higher frequencies of CD8

Indexed as

Antigens, ViralCOVID-19CytokinesAdultAge FactorsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChildFemaleHumansInfant, NewbornLeukocytes, MononuclearNucleocapsidPregnancySARS-CoV-2Spike Glycoprotein, CoronavirusAntigens, ViralCytokinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2childrenCOVID-19immune responseinflammationneonatespediatric immunologySARS-CoV-2spike protein

Identifiers

PMID36593041
PMCPMC9843773
OpenAlexW4313475286

What OpenQuestion holds

Textmetadata
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.