Cargando…

A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial

BACKGROUND: A subset of COPD-patients presents with eosinophilic airway inflammation. While treatment of asthmatic patients with the GATA3-specific DNAzyme SB010 attenuated sputum eosinophilia after allergen challenge, this specific treatment has not been evaluated in patients with COPD. Our objecti...

Descripción completa

Detalles Bibliográficos
Autores principales: Greulich, Timm, Hohlfeld, Jens M., Neuser, Petra, Lueer, Katrin, Klemmer, Andreas, Schade-Brittinger, Carmen, Harnisch, Susanne, Garn, Holger, Renz, Harald, Homburg, Ursula, Renz, Jonas, Kirsten, Anne, Pedersen, Frauke, Müller, Meike, Vogelmeier, Claus F., Watz, Henrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883532/
https://www.ncbi.nlm.nih.gov/pubmed/29615049
http://dx.doi.org/10.1186/s12931-018-0751-x
_version_ 1783311674304888832
author Greulich, Timm
Hohlfeld, Jens M.
Neuser, Petra
Lueer, Katrin
Klemmer, Andreas
Schade-Brittinger, Carmen
Harnisch, Susanne
Garn, Holger
Renz, Harald
Homburg, Ursula
Renz, Jonas
Kirsten, Anne
Pedersen, Frauke
Müller, Meike
Vogelmeier, Claus F.
Watz, Henrik
author_facet Greulich, Timm
Hohlfeld, Jens M.
Neuser, Petra
Lueer, Katrin
Klemmer, Andreas
Schade-Brittinger, Carmen
Harnisch, Susanne
Garn, Holger
Renz, Harald
Homburg, Ursula
Renz, Jonas
Kirsten, Anne
Pedersen, Frauke
Müller, Meike
Vogelmeier, Claus F.
Watz, Henrik
author_sort Greulich, Timm
collection PubMed
description BACKGROUND: A subset of COPD-patients presents with eosinophilic airway inflammation. While treatment of asthmatic patients with the GATA3-specific DNAzyme SB010 attenuated sputum eosinophilia after allergen challenge, this specific treatment has not been evaluated in patients with COPD. Our objective was to evaluate the feasibility and safety of inhaled SB010 in COPD patients with sputum eosinophilia. METHODS: We conducted a randomized, double-blind, placebo-controlled, multicentre clinical trial in COPD-patients with sputum eosinophilia (≥2.5% non-squamous cells). Patients inhaled 10 mg SB010 bid or matching placebo via the controlled inhalation system AKITA2 APIXNEB for 28 days. Endpoints included the feasibility of the study (primary), patient’s safety, sputum eosinophils, F(E)NO, lung function, symptoms, and biomarkers. The study was registered in the German Clinical Trials Register: DRKS00006087. RESULTS: One hundred thirty patients were screened, 23 patients were randomized (FEV(1) 49.4 ± 11.5%; sputum eosinophils 8.0 ± 8.4%) and 19 patients completed the study (10 placebo, 9 SB010. After 28 days, SB010 decreased the relative sputum eosinophil count (p = 0.004) as compared to no changes in placebo-treated patients. F(E)NO, lung function, and symptoms were not affected significantly. We found an increase in blood IFN-γ (p = 0.02) and a trend to lower IL-5 levels in patients treated with SB010. SB010 was safe and well tolerated. Thirty five AEs (22 SB010, 13 placebo including 1 SAE) were observed with 3 AEs in each group judged to be possibly treatment-related. CONCLUSION: In patients with eosinophilic COPD, sputum eosinophils could be reduced by inhalation of SB010. Long-term studies are needed to demonstrate clinical efficacy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0751-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5883532
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-58835322018-04-09 A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial Greulich, Timm Hohlfeld, Jens M. Neuser, Petra Lueer, Katrin Klemmer, Andreas Schade-Brittinger, Carmen Harnisch, Susanne Garn, Holger Renz, Harald Homburg, Ursula Renz, Jonas Kirsten, Anne Pedersen, Frauke Müller, Meike Vogelmeier, Claus F. Watz, Henrik Respir Res Research BACKGROUND: A subset of COPD-patients presents with eosinophilic airway inflammation. While treatment of asthmatic patients with the GATA3-specific DNAzyme SB010 attenuated sputum eosinophilia after allergen challenge, this specific treatment has not been evaluated in patients with COPD. Our objective was to evaluate the feasibility and safety of inhaled SB010 in COPD patients with sputum eosinophilia. METHODS: We conducted a randomized, double-blind, placebo-controlled, multicentre clinical trial in COPD-patients with sputum eosinophilia (≥2.5% non-squamous cells). Patients inhaled 10 mg SB010 bid or matching placebo via the controlled inhalation system AKITA2 APIXNEB for 28 days. Endpoints included the feasibility of the study (primary), patient’s safety, sputum eosinophils, F(E)NO, lung function, symptoms, and biomarkers. The study was registered in the German Clinical Trials Register: DRKS00006087. RESULTS: One hundred thirty patients were screened, 23 patients were randomized (FEV(1) 49.4 ± 11.5%; sputum eosinophils 8.0 ± 8.4%) and 19 patients completed the study (10 placebo, 9 SB010. After 28 days, SB010 decreased the relative sputum eosinophil count (p = 0.004) as compared to no changes in placebo-treated patients. F(E)NO, lung function, and symptoms were not affected significantly. We found an increase in blood IFN-γ (p = 0.02) and a trend to lower IL-5 levels in patients treated with SB010. SB010 was safe and well tolerated. Thirty five AEs (22 SB010, 13 placebo including 1 SAE) were observed with 3 AEs in each group judged to be possibly treatment-related. CONCLUSION: In patients with eosinophilic COPD, sputum eosinophils could be reduced by inhalation of SB010. Long-term studies are needed to demonstrate clinical efficacy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0751-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-04 2018 /pmc/articles/PMC5883532/ /pubmed/29615049 http://dx.doi.org/10.1186/s12931-018-0751-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Greulich, Timm
Hohlfeld, Jens M.
Neuser, Petra
Lueer, Katrin
Klemmer, Andreas
Schade-Brittinger, Carmen
Harnisch, Susanne
Garn, Holger
Renz, Harald
Homburg, Ursula
Renz, Jonas
Kirsten, Anne
Pedersen, Frauke
Müller, Meike
Vogelmeier, Claus F.
Watz, Henrik
A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial
title A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial
title_full A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial
title_fullStr A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial
title_full_unstemmed A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial
title_short A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial
title_sort gata3-specific dnazyme attenuates sputum eosinophilia in eosinophilic copd patients: a feasibility randomized clinical trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883532/
https://www.ncbi.nlm.nih.gov/pubmed/29615049
http://dx.doi.org/10.1186/s12931-018-0751-x
work_keys_str_mv AT greulichtimm agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT hohlfeldjensm agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT neuserpetra agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT lueerkatrin agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT klemmerandreas agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT schadebrittingercarmen agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT harnischsusanne agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT garnholger agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT renzharald agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT homburgursula agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT renzjonas agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT kirstenanne agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT pedersenfrauke agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT mullermeike agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT vogelmeierclausf agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT watzhenrik agata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT greulichtimm gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT hohlfeldjensm gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT neuserpetra gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT lueerkatrin gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT klemmerandreas gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT schadebrittingercarmen gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT harnischsusanne gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT garnholger gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT renzharald gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT homburgursula gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT renzjonas gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT kirstenanne gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT pedersenfrauke gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT mullermeike gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT vogelmeierclausf gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial
AT watzhenrik gata3specificdnazymeattenuatessputumeosinophiliaineosinophiliccopdpatientsafeasibilityrandomizedclinicaltrial