Evidence map›Paper›PMID 24183915›Full record

ArticleJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2014

BIIL 284 reduces neutrophil numbers but increases P. aeruginosa bacteremia and inflammation in mouse lungs.

Gerd Döring, Alessandra Bragonzi, Moira Paroni, Firdevs-Fatma Aktürk, Cristina Cigana, Annika Schmidt, Deirdre Gilpin, Susanne Heyder, Torsten Born, Christina Smaczny and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.5field-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

34 citing papers in PubMed, 69 citations in OpenAlex.

  1. Empire-CF study: A phase 2 clinical trial of leukotriene A4 hydrolase inhibitor acebilustat in adult subjects with cystic fibrosis.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2021
    Trial
  2. Trial
  3. Review
  4. Evaluation of ATP12A and NFKBIZ as potential markers of inflammatory status in cystic fibrosis airway epithelial cells.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  5. Dipeptidyl peptidase-1 inhibitors in bronchiectasis.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Pathogenesis of pneumonia and acute lung injury.Clinical science (London, England : 1979) · 2022
    Review
  12. Neutrophil extracellular traps in chronic lung disease: implications for pathogenesis and therapy.European respiratory review : an official journal of the European Respiratory Society · 2022
    Review
  13. The Effect of CFTR Modulators on Airway Infection in Cystic Fibrosis.International journal of molecular sciences · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  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

19 authors at 8 institutions in 4 countries.

Gerd DöringInstitute of Medical Microbiology and Hygiene, Universitätsklinikum Tübingen, Tübingen, Germany.
Alessandra BragonziInfection and Cystic Fibrosis Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy. Electronic address: bragonzi.alessandra@hsr.it.
Moira ParoniInfection and Cystic Fibrosis Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy.
Firdevs-Fatma AktürkInstitute of Medical Microbiology and Hygiene, Universitätsklinikum Tübingen, Tübingen, Germany.
Cristina CiganaInfection and Cystic Fibrosis Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy.
Annika SchmidtInstitute of Medical Microbiology and Hygiene, Universitätsklinikum Tübingen, Tübingen, Germany.
Deirdre GilpinQueen's University Belfast, Northern Ireland, UK.
Susanne HeyderKlinik Schillerhöhe, Robert-Bosch Krankenhaus, Gerlingen, Germany.
Torsten BornUniversitätsklinikum Frankfurt, Frankfurt, Germany.
Christina SmacznyUniversitätsklinikum Frankfurt, Frankfurt, Germany.
Martin KohlhäuflKlinik Schillerhöhe, Robert-Bosch Krankenhaus, Gerlingen, Germany.
Thomas O F WagnerUniversitätsklinikum Frankfurt, Frankfurt, Germany.
Michael R LoebingerRoyal Brompton Hospital, London, UK.
Diana BiltonRoyal Brompton Hospital, London, UK.
Michael M TunneyQueen's University Belfast, Northern Ireland, UK.
J Stuart ElbornQueen's University Belfast, Northern Ireland, UK.
Gerald B PierDivision of infectious Diseases, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Michael W KonstanCase Western Reserve University, UH Rainbow Babies & Children's Hospital, Cleveland, OH, USA.
Martina UlrichInstitute of Medical Microbiology and Hygiene, Universitätsklinikum Tübingen, Tübingen, Germany.
Universitätsklinikum Tübingen · DEGoethe University Frankfurt · DEQueen's University Belfast · GBVita-Salute San Raffaele University · ITRobert Bosch Hospital · DERoyal Brompton Hospital · GBBrigham and Women's Hospital · USRainbow Babies & Children's Hospital · US

Funding

Translational Research in Cystic FibrosisP30DK027651 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI DRUMM, MITCHELL L · 1986 to 2014
$15.6M
NIDDK NIH HHS P30 DK027651
6 · The paper itself

Abstract

backgroundA clinical study to investigate the leukotriene B(4) (LTB(4))-receptor antagonist BIIL 284 in cystic fibrosis (CF) patients was prematurely terminated due to a significantly increased risk of adverse pulmonary events. We aimed to establish the effect of BIIL284 in models of Pseudomonas aeruginosa lung infection, thereby contributing to a better understanding of what could have led to adverse pulmonary events in CF patients.

methodsP. aeruginosa DNA in the blood of CF patients during and after acute pulmonary exacerbations and in stable patients with non-CF bronchiectasis (NCFB) and healthy individuals was assessed by PCR. The effect of BIIL 284 treatment was tested in an agar bead murine model of P. aeruginosa lung infection. Bacterial count and inflammation were evaluated in lung and other organs.

resultsMost CF patients (98%) and all patients with NCFB and healthy individuals had negative P. aeruginosa DNA in their blood. Similarly, the P. aeruginosa-infected mice showed bacterial counts in the lung but not in the blood or spleen. BIIL 284 treatment decreased pulmonary neutrophils and increased P. aeruginosa numbers in mouse lungs leading to significantly higher bacteremia rates and lung inflammation compared to placebo treated animals.

conclusionsDecreased airway neutrophils induced lung proliferation and severe bacteremia in a murine model of P. aeruginosa lung infection. These data suggest that caution should be taken when administering anti-inflammatory compounds to patients with bacterial infections.

Indexed as

AmidinesCarbamatesCystic FibrosisNeutrophilsPseudomonas aeruginosaAdultAnimalsAnti-Inflammatory AgentsBacteremiaDisease Models, AnimalFemaleHumansInflammationLeukocyte CountLungMaleamelubantAmidinesAnti-Inflammatory AgentsCarbamatesReceptors, Leukotriene B4Anti-inflammatory treatmentCystic fibrosisPulmonary infection

Identifiers

PMID24183915
PMCPMC4163938
OpenAlexW2104893458

What OpenQuestion holds

Textmetadata
LicenceTDM
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.