Evidence map›Paper›PMID 34576313›Full record

ReviewInternational journal of molecular sciences2021

Eosinophils as Drivers of Severe Eosinophilic Asthma: Endotypes or Plasticity?

Glenn Van Hulst, Fabrice Bureau, Christophe J Desmet

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Exploring the therapeutic potential of monoclonal antibodies targeting TSLP and IgE in asthma management.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Review
  11. Article
  12. Article
  13. Radiation-Detoxified Form of Endotoxin Effectively Activates ThInternational journal of molecular sciences · 2024
    Article
  14. Review
  15. Review
  16. Article
  17. Subsets of Eosinophils in Asthma, a Challenge for Precise Treatment.International journal of molecular sciences · 2023
    Review
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Glenn Van HulstLaboratory of Cellular and Molecular Immunology, B34, GIGA Institute and Faculty of Veterinary Medicine, Liège University, 4000 Liège, Belgium.ORCID 0000-0003-3431-9127
Fabrice BureauLaboratory of Cellular and Molecular Immunology, B34, GIGA Institute and Faculty of Veterinary Medicine, Liège University, 4000 Liège, Belgium.ORCID 0000-0001-6264-4029
Christophe J DesmetLaboratory of Cellular and Molecular Immunology, B34, GIGA Institute and Faculty of Veterinary Medicine, Liège University, 4000 Liège, Belgium.ORCID 0000-0002-5723-2449
University of Liège · BE

Funding

Fonds De La Recherche Scientifique - FNRS 30565447 (U-HEAD)Fonds De La Recherche Scientifique - FNRS T.0052.18 REGEOS
6 · The paper itself

Abstract

Asthma is now recognized as a heterogeneous disease, encompassing different phenotypes driven by distinct pathophysiological mechanisms called endotypes. Common phenotypes of asthma, referred to as eosinophilic asthma, are characterized by the presence of eosinophilia. Eosinophils are usually considered invariant, terminally differentiated effector cells and have become a primary therapeutic target in severe eosinophilic asthma (SEA) and other eosinophil-associated diseases (EADs). Biological treatments that target eosinophils reveal an unexpectedly complex role of eosinophils in asthma, including in SEA, suggesting that "not all eosinophils are equal". In this review, we address our current understanding of the role of eosinophils in asthma with regard to asthma phenotypes and endotypes. We further address the possibility that different SEA phenotypes may involve differences in eosinophil biology. We discuss how these differences could arise through eosinophil "endotyping", viz. adaptations of eosinophil function imprinted during their development, or through tissue-induced plasticity, viz. local adaptations of eosinophil function through interaction with their lung tissue niches. In doing so, we also discuss opportunities, technical challenges, and open questions that, if addressed, might provide considerable benefits in guiding the choice of the most efficient precision therapies of SEA and, by extension, other EADs.

Indexed as

AnimalsAsthmaEosinophilsHumansImmunotherapyendotypeseosinophilic asthmaeosinophilseosinophil subsetsimmunotherapyplasticity

Identifiers

PMID34576313
PMCPMC8467265
OpenAlexW3201255943

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.