Evidence map›Paper›PMID 33484168›Full record

ArticleAllergy2021

Elastase and exacerbation of neutrophil innate immunity are involved in multi-visceral manifestations of COVID-19.

Jean-Louis Guéant, Rosa-Maria Guéant-Rodriguez, Julien Fromonot, Abderrahim Oussalah, Huguette Louis, Celine Chery, Mickael Gette, Stanislas Gleye, Jonas Callet, Jeremie Raso and 4 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Allergy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. Assessment of Patients With Beta-Lactams Positive Provocation Tests by Biomarkers of IgG-Related Neutrophil Activation.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2025
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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 1 institution in 1 country.

Jean-Louis GuéantDepartment Inserm, UMR_S 1256 Nutrition-Genetics-Environmental Risk Exposure, Université de Lorraine and University Regional hospital of Nancy, Nancy, France.ORCID 0000-0002-5067-042X
Rosa-Maria Guéant-RodriguezDepartment Inserm, UMR_S 1256 Nutrition-Genetics-Environmental Risk Exposure, Université de Lorraine and University Regional hospital of Nancy, Nancy, France.
Julien FromonotCenter for CardioVascular and Nutrition Research (RG, JF), INSERM, INRA and Aix-Marseille University, Marseille, France.
Abderrahim OussalahDepartment Inserm, UMR_S 1256 Nutrition-Genetics-Environmental Risk Exposure, Université de Lorraine and University Regional hospital of Nancy, Nancy, France.ORCID 0000-0002-9731-4529
Huguette LouisDepartment Inserm UMRS_1116 DCAC, Université de Lorraine, Nancy, France.
Celine CheryDepartment Inserm, UMR_S 1256 Nutrition-Genetics-Environmental Risk Exposure, Université de Lorraine and University Regional hospital of Nancy, Nancy, France.
Mickael GetteCenter for CardioVascular and Nutrition Research (RG, JF), INSERM, INRA and Aix-Marseille University, Marseille, France.
Stanislas GleyeDepartment Inserm, UMR_S 1256 Nutrition-Genetics-Environmental Risk Exposure, Université de Lorraine and University Regional hospital of Nancy, Nancy, France.
Jonas CalletDepartment Inserm, UMR_S 1256 Nutrition-Genetics-Environmental Risk Exposure, Université de Lorraine and University Regional hospital of Nancy, Nancy, France.
Jeremie RasoDepartment Inserm, UMR_S 1256 Nutrition-Genetics-Environmental Risk Exposure, Université de Lorraine and University Regional hospital of Nancy, Nancy, France.
François BlanchecotteMedical analysis laboratory L'ABO+, Chambray-les-Tours, France.
Patrick LacolleyDepartment Inserm UMRS_1116 DCAC, Université de Lorraine, Nancy, France.
Régis GuieuCenter for CardioVascular and Nutrition Research (RG, JF), INSERM, INRA and Aix-Marseille University, Marseille, France.
Véronique RegnaultDepartment Inserm UMRS_1116 DCAC, Université de Lorraine, Nancy, France.
Inserm · FR

Funding

FHU ARRIMAGELorraine Université d'Excellence ANR-15-IDEX-04-LUE
6 · The paper itself

Abstract

backgroundMany arguments suggest that neutrophils could play a prominent role in COVID-19. However, the role of key components of neutrophil innate immunity in severe forms of COVID-19 has deserved insufficient attention. We aimed to evaluate the involvement of neutrophil elastase, histone-DNA, and DNases in systemic and multi-organ manifestations of COVID-19.

methodsWe performed a multicenter study of markers of neutrophil innate immunity in 155 cases consecutively recruited in a screening center, local hospitals, and two regional university hospitals. The cases were evaluated according to clinical and biological markers of severity and multi-organ manifestations and compared to 35 healthy controls.

resultsBlood neutrophil elastase, histone-DNA, myeloperoxidase-DNA, and free dsDNA were dramatically increased, and DNase activity was decreased by 10-fold, compared with controls. Neutrophil elastase and histone-DNA were associated with intensive care admission, body temperature, lung damage, and markers of cardiovascular outcomes, renal failure, and increased interleukin-6 (IL-6), IL-8, and CXCR2. Neutrophil elastase was an independent predictor of the computed tomography score of COVID-19 lung damage and the number of affected organs, in multivariate analyses. The increased blood concentrations of NE and neutrophil extracellular traps were related to exacerbation of neutrophil stimulation through IL-8 and CXCR2 increased concentrations and increased serum DAMPs, and to impaired degradation of NETs as a consequence of the dramatic decrease in blood DNase activity.

conclusionOur results point out the key role of neutrophil innate immunity exacerbation in COVID-19. Neutrophil elastase and DNase could be potential biomarkers and therapeutic targets of severe systemic manifestations of COVID-19.

Indexed as

COVID-19Extracellular TrapsHistonesHumansImmunity, InnateNeutrophilsSARS-CoV-2HistonesCOVID-19DNaseinnate immunitymyeloperoxidaseneutrophil extracellular traps (NETs)

Identifiers

PMID33484168
PMCPMC8014109
OpenAlexW3125872925

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.