Evidence map›Paper›PMID 31613219›Full record

ArticleeLife2019

Inhibition of ErbB kinase signalling promotes resolution of neutrophilic inflammation.

Atiqur Rahman, Katherine M Henry, Kimberly D Herman, Alfred Ar Thompson, Hannah M Isles, Claudia Tulotta, David Sammut, Julien Jy Rougeot, Nika Khoshaein, Abigail E Reese and 10 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. The Multifaceted Roles of Neutrophil Death in COPD and Lung Cancer.Journal of respiratory biology and translational medicine · 2025
    Article
  8. Review
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  13. Article
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  15. Common mechanism ofChinese herbal medicines · 2021
    Article
  16. Article
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  18. 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

20 authors at 6 institutions in 4 countries.

Atiqur RahmanDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Katherine M HenryDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.ORCID 0000-0003-0554-2063
Kimberly D HermanDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Alfred Ar ThompsonDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.ORCID 0000-0002-0717-4551
Hannah M IslesDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Claudia TulottaDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
David SammutDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Julien Jy RougeotInstitute of Biology, Leiden University, Leiden, Netherlands.
Nika KhoshaeinDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Abigail E ReeseDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Kathryn HigginsDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Caroline TaborThe Bateson Centre, University of Sheffield, Sheffield, United Kingdom.
Ian SabroeDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
William J ZuercherSGC-UNC, Division of Chemical Biology and Medicinal Chemistry, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, United States.
Caroline O SavageImmuno-Inflammation Therapy Area Unit, GlaxoSmithKline Research and Development Ltd, Stevenage, United Kingdom.
Annemarie H MeijerInstitute of Biology, Leiden University, Leiden, Netherlands.
Moira Kb WhyteMRC Centre for Inflammation Research, University of Edinburgh, Edinburgh, United Kingdom.
David H DockrellDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Stephen A Renshaw *Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.ORCID 0000-0003-1790-1641
Lynne R Prince *Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.ORCID 0000-0001-6133-9372
University of Sheffield · GBCentre for Inflammation Research · GBLeiden University · NLGlaxoSmithKline (United Kingdom) · GBUniversity of Dhaka · BDUniversity of North Carolina at Chapel Hill · US

Funding

British Heart Foundation Intermediate Clinician Fellowship FS/18/13/33281European Commission PITG-GA-2011-289209Medical Research Council G0700091Medical Research Council MC_PC_12022Medical Research Council MR/M004864/1Medical Research Council MR/N02995X/1Medical Research Council MR/P020941/1
6 · The paper itself

Abstract

Neutrophilic inflammation with prolonged neutrophil survival is common to many inflammatory conditions, including chronic obstructive pulmonary disease (COPD). There are few specific therapies that reverse neutrophilic inflammation, but uncovering mechanisms regulating neutrophil survival is likely to identify novel therapeutic targets. Screening of 367 kinase inhibitors in human neutrophils and a zebrafish tail fin injury model identified ErbBs as common targets of compounds that accelerated inflammation resolution. The ErbB inhibitors gefitinib, CP-724714, erbstatin and tyrphostin AG825 significantly accelerated apoptosis of human neutrophils, including neutrophils from people with COPD. Neutrophil apoptosis was also increased in Tyrphostin AG825 treated-zebrafish in vivo. Tyrphostin AG825 decreased peritoneal inflammation in zymosan-treated mice, and increased lung neutrophil apoptosis and macrophage efferocytosis in a murine acute lung injury model. Tyrphostin AG825 and knockdown of

Indexed as

Animal FinsAnimalsBenzothiazolesCells, CulturedDisease Models, AnimalErbB ReceptorsHumansInflammationLungMiceNeutrophilsPneumonia, BacterialProtein Kinase InhibitorsPseudomonas InfectionsTreatment OutcomeTyrphostinsBenzothiazolesEGFR protein, humanEGFR protein, mouseErbB ReceptorsProtein Kinase Inhibitorstyrphostin AG825Tyrphostinsapoptosishumanimmunologyinflammationmouseneutrophilprotein kinasezebrafish

Identifiers

PMID31613219
PMCPMC6839918
OpenAlexW2980719126

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.