Evidence map›Paper›PMID 34659235›Full record

ArticleFrontiers in immunology2021

Asymptomatic and Mild SARS-CoV-2 Infections Elicit Lower Immune Activation and Higher Specific Neutralizing Antibodies in Children Than in Adults.

Maria Raffaella Petrara, Francesco Bonfante, Paola Costenaro, Anna Cantarutti, Francesco Carmona, Elena Ruffoni, Costanza Di Chiara, Marisa Zanchetta, Luisa Barzon, Daniele Donà and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 53 citations in OpenAlex.

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  7. T Regulatory Cell Subsets Do Not Restore for One Year After Acute COVID-19.International journal of molecular sciences · 2024
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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

19 authors at 6 institutions in 1 country.

Maria Raffaella PetraraOncology and Immunology Section, Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
Francesco BonfanteDepartment of Comparative Biomedical Sciences, Istituto Zooprofilattico Sperimentale delle Venezie (IZSVe), Virology Laboratory, Legnaro, Italy.
Paola CostenaroDivision of Pediatric Infectious Diseases, Department for Women's and Children's Health, University of Padova, Padova, Italy.
Anna CantaruttiLaboratory of Healthcare Research and Pharmacoepidemiology, Department of Statistics and Quantitative Methods, University of Milano-Bicocca, Milano, Italy.
Francesco CarmonaImmunology and Diagnostic Molecular Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Elena RuffoniImmunology and Diagnostic Molecular Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Costanza Di ChiaraDivision of Pediatric Infectious Diseases, Department for Women's and Children's Health, University of Padova, Padova, Italy.
Marisa ZanchettaImmunology and Diagnostic Molecular Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Luisa BarzonDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Daniele DonàDivision of Pediatric Infectious Diseases, Department for Women's and Children's Health, University of Padova, Padova, Italy.
Liviana Da DaltDivision of Pediatric Infectious Diseases, Department for Women's and Children's Health, University of Padova, Padova, Italy.
Alessio BortolamiDepartment of Comparative Biomedical Sciences, Istituto Zooprofilattico Sperimentale delle Venezie (IZSVe), Virology Laboratory, Legnaro, Italy.
Matteo PagliariDepartment of Comparative Biomedical Sciences, Istituto Zooprofilattico Sperimentale delle Venezie (IZSVe), Virology Laboratory, Legnaro, Italy.
Mario PlebaniDepartment of Laboratory Medicine, University-Hospital of Padova, Padova, Italy.
Paolo RossiClinical and Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Nicola CotugnoClinical and Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Paolo PalmaClinical and Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Carlo GiaquintoDivision of Pediatric Infectious Diseases, Department for Women's and Children's Health, University of Padova, Padova, Italy.
Anita De RossiOncology and Immunology Section, Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
University of Padua · ITIstituto Oncologico Veneto · ITIstituto Zooprofilattico Sperimentale delle Venezie · ITBambino Gesù Children's Hospital · ITUniversity of Milano-Bicocca · ITUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The immune response plays a pivotal role in dictating the clinical outcome in severe acute respiratory syndrome coronavirus 2 (SARS Methods: Of 209 enrolled subjects, 155 patients were confirmed by PCR and/or serology as having coronavirus disease 2019 (COVID-19). Blood samples were obtained at a median of 2.8 (interquartile, 2.1-3.7) and 6.1 (5.3-7.2) months after baseline (symptom onset and/or first positive virus detection). The immune profiles of activation, senescence, exhaustion, and regulatory cells were analyzed by flow cytometry. Neutralizing antibodies (nAbs) were detected by a plaque reduction neutralization test. In available nasopharyngeal swabs at baseline, SARS-CoV-2 levels were quantified by digital droplet PCR (ddPCR). Results: Overall, COVID-19 patients had higher levels of immune activation, exhaustion, and regulatory cells compared to non-COVID-19 subjects. Within the COVID-19 group, activated and senescent cells were higher in adults than in children and inversely correlated with the nAbs levels. Conversely, Tregs and Bregs regulatory cells were higher in COVID-19 children compared to adults and positively correlated with nAbs. Higher immune activation still persisted in adults after 6 months of infection, while children maintained higher levels of regulatory cells. SARS-CoV-2 levels did not differ among age classes. Conclusions: Adults displayed higher immune activation and lower production of anti-SARS-CoV-2 nAbs than children. The different immune response was not related to different viral load. The higher expression of regulatory cells in children may contribute to reduce the immune activation, thus leading to a greater specific response against the virus.

Indexed as

Asymptomatic InfectionsAdultAntibodies, NeutralizingAntibodies, ViralB-Lymphocytes, RegulatoryChildChild, PreschoolCOVID-19CytokinesFemaleHumansLymphocyte CountMaleMiddle AgedPathogen-Associated Molecular Pattern MoleculesProspective StudiesAntibodies, NeutralizingAntibodies, ViralCytokinesPathogen-Associated Molecular Pattern MoleculesCOVID-19 childrenimmune activationneutralizing antibodies (NAbs)senescenceTregs and Bregs

Identifiers

PMID34659235
PMCPMC8515185
OpenAlexW3203388792

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Registered trials

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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.