Evidence map›Paper›PMID 27215684›Full record

ArticleScientific reports2016

Reducing hypoxia and inflammation during invasive pulmonary aspergillosis by targeting the Interleukin-1 receptor.

Mark S Gresnigt, Abdessalem Rekiki, Orhan Rasid, Amélie Savers, Grégory Jouvion, Eric Dannaoui, Marianna Parlato, Catherine Fitting, Matthias Brock, Jean-Marc Cavaillon and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–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

35 citing papers in PubMed.

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  15. Novel Insights intoJournal of fungi (Basel, Switzerland) · 2022
    Review
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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

12 authors.

Mark S GresnigtUnité de recherche Cytokines &Inflammation, Institut Pasteur, Paris.
Abdessalem RekikiPFID, Bioaster, Institut Pasteur, Paris France.
Orhan RasidUnité de recherche Cytokines &Inflammation, Institut Pasteur, Paris.
Amélie SaversFungal Genetics and Biology, School of Life Sciences, University of Nottingham, UK.
Grégory JouvionUnité Histopathologie Humaine et Modèles Animaux, Institut Pasteur, Paris France.
Eric DannaouiParis-Descartes University, Faculty of Medicine, APHP, European Georges Pompidou Hospital, Parasitology-Mycology Unit, Microbiology department, Paris, France.
Marianna ParlatoINSERM UMR S1163 Institut Imagine, Laboratoire d'Immunité Intestinale, Paris France.
Catherine FittingUnité de recherche Cytokines &Inflammation, Institut Pasteur, Paris.
Matthias BrockFungal Genetics and Biology, School of Life Sciences, University of Nottingham, UK.
Jean-Marc CavaillonUnité de recherche Cytokines &Inflammation, Institut Pasteur, Paris.
Frank L van de VeerdonkDepartment of Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Oumaïma Ibrahim-GranetUnité de recherche Cytokines &Inflammation, Institut Pasteur, Paris.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypoxia as a result of pulmonary tissue damage due to unresolved inflammation during invasive pulmonary aspergillosis (IPA) is associated with a poor outcome. Aspergillus fumigatus can exploit the hypoxic microenvironment in the lung, but the inflammatory response required for fungal clearance can become severely disregulated as a result of hypoxia. Since severe inflammation can be detrimental to the host, we investigated whether targeting the interleukin IL-1 pathway could reduce inflammation and tissue hypoxia, improving the outcome of IPA. The interplay between hypoxia and inflammation was investigated by in vivo imaging of hypoxia and measurement of cytokines in the lungs in a model of corticosteroid immunocompromised and in Cxcr2 deficient mice. Severe hypoxia was observed following Aspergillus infection in both models and correlated with development of pulmonary inflammation and expression of hypoxia specific transcripts. Treatment with IL-1 receptor antagonist reduced hypoxia and slightly, but significantly reduced mortality in immunosuppressed mice, but was unable to reduce hypoxia in Cxcr2(-/-) mice. Our data provides evidence that the inflammatory response during invasive pulmonary aspergillosis, and in particular the IL-1 axis, drives the development of hypoxia. Targeting the inflammatory IL-1 response could be used as a potential immunomodulatory therapy to improve the outcome of aspergillosis.

Indexed as

Adrenal Cortex HormonesAnimalsCarbonic Anhydrase IXCell HypoxiaCytokinesDisease Models, AnimalImmunocompromised HostInterleukin 1 Receptor Antagonist ProteinInvasive Pulmonary AspergillosisMiceReceptors, Interleukin-1Receptors, Interleukin-8BTreatment OutcomeAdrenal Cortex HormonesCar9 protein, mouseCarbonic Anhydrase IXCytokinesInterleukin 1 Receptor Antagonist ProteinReceptors, Interleukin-1Receptors, Interleukin-8B

Identifiers

PMID27215684
PMCPMC4877709

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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.