Evidence map›Paper›PMID 34889061›Full record

ArticleImmunity, inflammation and disease2022

Anakinra reduces lung inflammation in experimental acute lung injury.

Paul Engeroff, Aude Belbézier, Antoine Monsel, David Klatzmann

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Immune modulatory potential ofToxicology research · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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

4 authors at 1 institution in 1 country.

Paul EngeroffINSERM, Immunology-Immunopathology-Immunotherapy Department (i3), Sorbonne Université, Paris, France.ORCID 0000-0002-3409-512X
Aude BelbézierINSERM, Immunology-Immunopathology-Immunotherapy Department (i3), Sorbonne Université, Paris, France.ORCID 0000-0002-6505-6596
Antoine MonselINSERM, Immunology-Immunopathology-Immunotherapy Department (i3), Sorbonne Université, Paris, France.ORCID 0000-0002-9647-7043
David KlatzmannINSERM, Immunology-Immunopathology-Immunotherapy Department (i3), Sorbonne Université, Paris, France.ORCID 0000-0002-0054-3422
Inserm · FR

Funding

Agence Nationale de la Recherche ANR-11-IDEX-0004-02Agence Nationale de la Recherche LabEx TransimmunomSchweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung P2BEP3_188262
6 · The paper itself

Abstract

introductionAcute respiratory distress syndrome (ARDS) is a severe form of acute lung injury (ALI) resulting in life-threatening hypoxaemia. Although ARDS can be caused by a variety of pathogens or major trauma, it is best known as the major cause of mortality in COVID-19 patients. Since ARDS is often associated with dysregulated inflammatory immune responses, immunomodulatory approaches represent a possible treatment option. The objective of this study was to evaluate the therapeutic potential of interleukin (IL)-1 blockade using Anakinra in a mouse model of lipopolysaccharide (LPS)-induced ALI.

methodsWe evaluated the effects of a daily subcutaneous Anakinra treatment in a mouse model of LPS-induced ALI. We monitored body weight to assess the general health status of the mice. Two days after ALI induction, we evaluated the inflammatory cytokine MIP-2 as well as protein levels in bronchoalveolar lavage (BAL) fluids. Two and nine days after ALI induction, we evaluated infiltrating leukocytes in BAL fluid and lung tissue.

resultsAnakinra treatment reduced ALI-induced weight loss compared to nontreated groups. At Day 2, Anakinra treatment reduced levels of MIP-2 and protein in BAL fluids and reduced frequencies of NK cells and neutrophils in the lung tissue. Nine days after ALI induction, Anakinra treated mice displayed reduced levels of neutrophils and alveolar macrophages in BAL fluids.

conclusionsIL-1 blockade using Anakinra reduced classical hallmarks of inflammation in a mouse model of ALI. Our data support ongoing and future research on the evaluation of Anakinra as a potential treatment option in ARDS.

Indexed as

Acute Lung InjuryCOVID-19PneumoniaAnimalsHumansInterleukin 1 Receptor Antagonist ProteinMiceSARS-CoV-2Interleukin 1 Receptor Antagonist Proteincovid-19IL-1IL-1Raimmunotherapyrespiratory distress syndrome

Identifiers

PMID34889061
PMCPMC8767508
OpenAlexW4200371425

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.