Evidence map›Paper›PMID 36271745›Full record

ArticleEuropean journal of immunology2022

IL-13 determines specific IgE responses and SARS-CoV-2 immunity after mild COVID-19 and novel mRNA vaccination.

Stefan Meltendorf, Katrin Vogel, Christoph Thurm, Florian Prätsch, Annegret Reinhold, Jacqueline Färber, Hans-Gert Heuft, Achim J Kaasch, Thomas Hachenberg, Stefan Weinzierl and 4 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 11 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

14 authors at 3 institutions in 1 country.

Stefan MeltendorfDepartment of Experimental Pediatrics, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Katrin VogelDepartment of Experimental Pediatrics, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Christoph ThurmInstitute of Molecular and Clinical Immunology, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Florian PrätschDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Annegret ReinholdInstitute of Molecular and Clinical Immunology, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Jacqueline FärberInstitute of Medical Microbiology and Hospital Hygiene, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Hans-Gert HeuftDepartment of Transfusion Medicine and Immunohematology, University Hospital Magdeburg, Magdeburg, Germany.
Achim J KaaschInstitute of Medical Microbiology and Hospital Hygiene, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Thomas HachenbergDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Magdeburg, Magdeburg, Germany.
Stefan WeinzierlAudio-Communication Group, Technical University Berlin, Berlin, Germany.
Burkhart SchravenInstitute of Molecular and Clinical Immunology, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Dirk ReinholdInstitute of Molecular and Clinical Immunology, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Monika C Brunner-WeinzierlDepartment of Experimental Pediatrics, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Holger LingelDepartment of Experimental Pediatrics, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Otto-von-Guericke University Magdeburg · DEUniversity Hospital Magdeburg · DETechnische Universität Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

After recovery, mild and severe COVID-19 diseases are associated with long-term effects on the host immune system, such as prolonged T-cell activation or accumulation of autoantibodies. In this study, we show that mild SARS-CoV-2 infections, but not SARS-CoV-2 spike mRNA vaccinations, cause durable atopic risk factors such as a systemic Th2- and Th17-type environment as well as activation of B cells responsive of IgE against aeroallergens from house dust mite and mold. At an average of 100 days post mild SARS-CoV-2 infections, anti-mold responses were associated with low IL-13 levels and increased pro-inflammatory IL-6 titers. Acutely severely ill COVID-19 patients instead showed no evidence of atopic reactions. Considering convalescents of mild COVID-19 courses and mRNA-vaccinated individuals together, IL-13 was the predominant significantly upregulated factor, likely shaping SARS-CoV-2 immunity. Application of multiple regression analysis revealed that the IL-13 levels of both groups were determined by the Th17-type cytokines IL-17A and IL-22. Taken together, these results implicate a critical role for IL-13 in the aftermath of SARS-CoV-2 mild infections and mRNA vaccinations, conferring protection against airway directed, atopic side reactions that occur in mildly experienced COVID-19.

Indexed as

COVID-19COVID-19 VaccinesHypersensitivity, ImmediateImmunoglobulin EInterleukin-13HumansmRNA VaccinesSARS-CoV-2VaccinationCOVID-19 VaccinesImmunoglobulin EInterleukin-13mRNA VaccinesAllergyCOVID-19CytokinesSARS-CoV-2Vaccination

Identifiers

PMID36271745
PMCPMC9874813
OpenAlexW4307067867

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.