posted on 2019-07-08, 08:42authored byL George, A Wright, V Mistry, A Sutcliffe, L Chachi, K Haldar, MY Ramsheh, M Richardson, R van der Merwe, U Martin, P Newbold, CE Brightling
We hypothesized whether the reduction in eosinophilic airway inflammation in patients with chronic obstructive pulmonary disease (COPD) following treatment with benralizumab, a humanized, afucosylated, monoclonal antibody that binds to interleukin-5 receptor α, increases the airway bacterial load. Analysis of sputum samples of COPD patients participating in a Phase II trial of benralizumab indicated that sputum 16S rDNA load and Streptococcus pneumoniae were reduced following treatment with benralizumab. However, in vitro, eosinophils did not affect the killing of the common airway pathogens S. pneumoniae or Haemophilus influenzae. Thus, benralizumab may have an indirect effect upon airway bacterial load.
Funding
Editorial support was
provided by Cactus Communications and by Michael
A Nissen, ELS, of AstraZeneca. This support was funded by
AstraZeneca. This work was funded in part by Airway Disease
PRedicting Outcomes through Patient Specific Computational
Modelling (AirPROM) project (funded through the European
Union’s Seventh Framework Programme [FP7] grant), the
National Institute for Health Research (NIHR) Leicester
Respiratory Biomedical Centre, and MedImmune Ltd.
History
Citation
International Journal of Chronic Obstructive Pulmonary Disease, 2019, 14, pp. 1177-1185
Author affiliation
/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Department of Infection, Immunity and Inflammation
Version
VoR (Version of Record)
Published in
International Journal of Chronic Obstructive Pulmonary Disease