Evidence map›Paper›PMID 33391280›Full record

Trial reportFrontiers in immunology2020

Different Innate and Adaptive Immune Responses to SARS-CoV-2 Infection of Asymptomatic, Mild, and Severe Cases.

Rita Carsetti, Salvatore Zaffina, Eva Piano Mortari, Sara Terreri, Francesco Corrente, Claudia Capponi, Patrizia Palomba, Mattia Mirabella, Simona Cascioli, Paolo Palange and 20 more

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 5 pooled it
–field-weighted citation impact
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

125 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
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  14. Observational
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65 more citing papers are in PubMed but not listed here.

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

30 authors.

Rita CarsettiB Cell Pathophysiology Unit, Immunology Research Area, Bambino Gesù Children's Hospital Istituto di Ricovero e Cura a Carattere Scientifico (IRCSS), Rome, Italy.
Salvatore ZaffinaOccupational Medicine/Health Technology Assessment and Safety Research Unit, Clinical-Technological Innovations Research Area, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
Eva Piano MortariB Cell Pathophysiology Unit, Immunology Research Area, Bambino Gesù Children's Hospital Istituto di Ricovero e Cura a Carattere Scientifico (IRCSS), Rome, Italy.
Sara TerreriB Cell Pathophysiology Unit, Immunology Research Area, Bambino Gesù Children's Hospital Istituto di Ricovero e Cura a Carattere Scientifico (IRCSS), Rome, Italy.
Francesco CorrenteDiagnostic Immunology Unit, Department of Laboratories, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Claudia CapponiDiagnostic Immunology Unit, Department of Laboratories, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Patrizia PalombaDiagnostic Immunology Unit, Department of Laboratories, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Mattia MirabellaDiagnostic Immunology Unit, Department of Laboratories, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Simona CascioliResearch Laboratories, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Paolo PalangeDepartment of Public Health and Infectious Diseases Pulmonary Division, Policlinico Umberto I Hospital, Rome, Italy.
Ilaria CuccaroDepartment of Public Health and Infectious Diseases Pulmonary Division, Policlinico Umberto I Hospital, Rome, Italy.
Cinzia MilitoDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Alimuddin ZumlaCenter for Clinical Microbiology, Division of Infection and Immunity, University College London, London, United Kingdom.
Markus MaeurerImmunotherapy Programme, Champalimaud Foundation, Lisbon, Portugal.
Vincenzo CamisaOccupational Medicine/Health Technology Assessment and Safety Research Unit, Clinical-Technological Innovations Research Area, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
Maria Rosaria VinciOccupational Medicine/Health Technology Assessment and Safety Research Unit, Clinical-Technological Innovations Research Area, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
Annapaola SantoroOccupational Medicine/Health Technology Assessment and Safety Research Unit, Clinical-Technological Innovations Research Area, Bambino Gesù Children's Hospital, IRCSS, Rome, Italy.
Eleonora CiminiCellular Immunology Laboratory, INMI L Spallanzani, IRCCS, Rome, Italy.
Luisa MarchioniClinical Department, INMI L Spallanzani, IRCCS, Rome, Italy.
Emanuele NicastriClinical Department, INMI L Spallanzani, IRCCS, Rome, Italy.
Fabrizio PalmieriClinical Department, INMI L Spallanzani, IRCCS, Rome, Italy.
Chiara AgratiCellular Immunology Laboratory, INMI L Spallanzani, IRCCS, Rome, Italy.
Giuseppe IppolitoScientific Direction, INMI L Spallanzani, IRCCS, Rome, Italy.
Ottavia PorzioMedical Laboratory Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Carlo ConcatoVirology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Andrea Onetti MudaDepartment of Laboratories, Bambino Gesù Children's Hospital, Rome, Italy.
Massimiliano RaponiHealth Directorate, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy.
Concetta QuintarelliDepartment of Hematology/Oncology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Isabella QuintiDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Franco LocatelliDepartment of Hematology/Oncology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SARS-CoV-2 is a novel coronavirus, not encountered before by humans. The wide spectrum of clinical expression of SARS-CoV-2 illness suggests that individual immune responses to SARS-CoV-2 play a crucial role in determining the clinical course after first infection. Immunological studies have focused on patients with moderate to severe disease, demonstrating excessive inflammation in tissues and organ damage. In order to understand the basis of the protective immune response in COVID-19, we performed a longitudinal follow-up, flow-cytometric and serological analysis of innate and adaptive immunity in

Indexed as

Adaptive ImmunityImmunity, InnateAdultAntibodies, ViralCOVID-19FemaleHumansImmunoglobulin AImmunoglobulin MKiller Cells, NaturalMaleSARS-CoV-2Severity of Illness IndexAntibodies, ViralImmunoglobulin AImmunoglobulin MantibodiesB cellsCOVID-19innate and adaptiveimmune responsemonocytesNK cellSARS-CoV-2

Identifiers

PMID33391280
PMCPMC7772470

What OpenQuestion holds

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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.