Evidence map›Paper›PMID 32463803›Full record

ArticleThe Journal of clinical investigation2020

Impaired immune cell cytotoxicity in severe COVID-19 is IL-6 dependent.

Alessio Mazzoni, Lorenzo Salvati, Laura Maggi, Manuela Capone, Anna Vanni, Michele Spinicci, Jessica Mencarini, Roberto Caporale, Benedetta Peruzzi, Alberto Antonelli and 19 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 344 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
344citing papers in PubMed, 1 pooled it
11.7field-weighted citation impact, top 1% 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

344 citing papers in PubMed, 1 synthesis or guideline pooled it, 531 citations in OpenAlex.

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  13. T-cell exhaustion and antibody response in SARS-CoV-2 vaccine recipients.Revista peruana de medicina experimental y salud publica · 2025
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284 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

29 authors at 7 institutions in 7 countries.

Alessio MazzoniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Lorenzo SalvatiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Laura MaggiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Manuela CaponeDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Anna VanniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Michele SpinicciDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Jessica MencariniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Roberto CaporaleFlow Cytometry Diagnostic Center and Immunotherapy (CDCI).
Benedetta PeruzziFlow Cytometry Diagnostic Center and Immunotherapy (CDCI).
Alberto AntonelliDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Michele TrottaInfectious and Tropical Diseases Unit.
Lorenzo ZammarchiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Luca CianiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Leonardo GoriDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Chiara LazzeriIntensive Care Unit and Regional Extracorporeal Membrane Oxygenation (ECMO) Referral Centre.
Andrea MatucciImmunoallergology Unit.
Alessandra VultaggioImmunoallergology Unit.
Oliviero RossiImmunoallergology Unit.
Fabio AlmerigognaDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Paola ParronchiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Paolo FontanariCardiac Anesthesia and Intensive Care Unit.
Federico LavoriniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Adriano PerisIntensive Care Unit and Regional Extracorporeal Membrane Oxygenation (ECMO) Referral Centre.
Gian Maria RossoliniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Alessandro BartoloniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Sergio RomagnaniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Francesco LiottaDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Francesco AnnunziatoDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Lorenzo CosmiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
University of Florence · ITHospital for Tropical Diseases · VNEuromedic · PLFraunhofer Institute for Cell Therapy and Immunology · DEOffice of Extramural Research · USIntensive Care Society · GBSan Diego Cardiac Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUNDCoronavirus disease 19 (COVID-19) is an emerging infectious disease caused by SARS-CoV-2. Antiviral immune response is crucial to achieve pathogen clearance; however, in some patients an excessive and aberrant host immune response can lead to an acute respiratory distress syndrome. The comprehension of the mechanisms that regulate pathogen elimination, immunity, and pathology is essential to better characterize disease progression and widen the spectrum of therapeutic options.METHODSWe performed a flow cytometric characterization of immune cell subsets from 30 patients with COVID-19 and correlated these data with clinical outcomes.RESULTSPatients with COVID-19 showed decreased numbers of circulating T, B, and NK cells and exhibited a skewing of CD8+ T cells toward a terminally differentiated/senescent phenotype. In agreement, CD4+ T and CD8+ T, but also NK cells, displayed reduced antiviral cytokine production capability. Moreover, a reduced cytotoxic potential was identified in patients with COVID-19, particularly in those who required intensive care. The latter group of patients also showed increased serum IL-6 levels that inversely correlated to the frequency of granzyme A-expressing NK cells. Off-label treatment with tocilizumab restored the cytotoxic potential of NK cells.CONCLUSIONThe association between IL-6 serum levels and the impairment of cytotoxic activity suggests the possibility that targeting this cytokine may restore antiviral mechanisms.FUNDINGThis study was supported by funds from the Department of Experimental and Clinical Medicine of University of Florence (the ex-60% fund and the "Excellence Departments 2018-2022 Project") derived from Ministero dell'Istruzione, dell'Università e della Ricerca (Italy).

Indexed as

BetacoronavirusCytotoxicity, ImmunologicAdultAgedAged, 80 and overB-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCoronavirus InfectionsCOVID-19Critical CareCytokinesFemaleGranzymesHumansInterleukin-6CytokinesGranzymesGZMA protein, humanIL6 protein, humanInterleukin-6Cellular immune responseCytokinesImmunologyInfectious diseaseNK cells

Identifiers

PMID32463803
PMCPMC7456250
OpenAlexW3032533580

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.