Evidence map›Paper›PMID 32870529›Full record

ArticleImmunology2020

Quantitative and qualitative alterations of circulating myeloid cells and plasmacytoid DC in SARS-CoV-2 infection.

Benedetta Peruzzi, Sara Bencini, Manuela Capone, Alessio Mazzoni, Laura Maggi, Lorenzo Salvati, Anna Vanni, Chiara Orazzini, Carlo Nozzoli, Alessandro Morettini and 9 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
6.5field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. JAK inhibitors and COVID-19.Journal for immunotherapy of cancer · 2022
    Pooled it
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 1 country.

Benedetta PeruzziFlow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.
Sara BenciniFlow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.
Manuela CaponeDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Alessio MazzoniDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Laura MaggiDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Lorenzo SalvatiDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Anna VanniDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Chiara OrazziniFlow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.
Carlo NozzoliInternal Medicine Unit 1, AOU Careggi, Florence, Italy.
Alessandro MorettiniInternal Medicine Unit 2, AOU Careggi, Florence, Italy.ORCID 0000-0002-7101-9599
Loredana PoggesiDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Filippo PieralliHigh Intensity Internal Medicine, AOU Careggi, Florence, Italy.
Adriano PerisIntensive Care Unit, AOU Careggi, Florence, Italy.
Alessandro BartoloniDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Alessandro Maria VannucchiDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Francesco LiottaDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Roberto CaporaleFlow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.
Lorenzo CosmiDepartment of Clinical and Experimental Medicine, University of Florence, Florence, Italy.
Francesco AnnunziatoFlow Cytometry Diagnostic Center and Immunotherapy (CDCI), AOU Careggi, Florence, Italy.ORCID 0000-0001-8798-7589
Azienda Ospedaliero-Universitaria Careggi · ITUniversity of Florence · IT

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca Excellence Departments 2018-2022 Project
6 · The paper itself

Abstract

SARS-CoV-2 is responsible for a new infectious disease (COVID-19) in which individuals can either remain asymptomatic or progress from mild to severe clinical conditions including acute respiratory distress syndrome and multiple organ failure. The immune mechanisms that potentially orchestrate the pathology in SARS-CoV-2 infection are complex and only partially understood. There is still paucity of data on the features of myeloid cells involved in this viral infection. For this reason, we investigated the different activation status profiles and the subset distribution of myeloid cells and their correlation with disease progression in 40 COVID-19 patients at different stages of disease. COVID-19 patients showed a decrease in the absolute number of plasmacytoid and myeloid dendritic cells, different subset distribution of monocytes and different activation patterns of both monocytes and neutrophils, coupled to a significant reduction of HLA-DR monocyte levels. We found that some of these alterations are typical of all COVID-19 patients, while some others vary at different stages of the disease and correlate with biochemical parameters of inflammation. Collectively, these data suggest that not only the lymphoid, but also the myeloid compartment, is severely affected by SARS-CoV-2 infection.

Indexed as

AdultAgedCOVID-19Dendritic CellsFemaleFlow CytometryHumansIntensive Care UnitsMaleMyeloid Cells

Identifiers

PMID32870529
PMCPMC7692244
OpenAlexW3082675822

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.