COPD_A_198302 1177..1185

Introduction Chronic obstructive pulmonary disease (COPD) is characterized by irreversible airflow obstruction and airway inflammation. Although typically neutrophilic, COPD is eosinophil-predominant in 10%‒40% of cases. Increased airway or blood eosinophil counts are associated with a good response to corticosteroids in stable COPD and during exacerbations. Interleukin-5 (IL-5) binds with high affinity to the IL-5 receptor (R) alpha (IL-5Rα) subunit and plays a pivotal role in the differentiation andmaturation of eosinophils in the bone marrow and their survival in tissue. In a 1-year randomized placebo-controlled trial of benralizumab, a humanized, afucosylated, monoclonal antibody that inhibits IL-5Rα activation and promotes antibody-dependent cellmediated cytotoxicity (leading to near complete eosinophil depletion), improvements in lung function and symptoms and reduction in exacerbations were observed in patients with eosinophilic inflammation. However, in non-eosinophilic COPD patients, exacerbation frequency increased following benralizumab treatment vs placebo. Likewise, in a 6-month trial, the IL-5 neutralizing monoclonal antibody mepolizumab reduced exacerbations vs placebo in COPD patients with an increased blood eosinophil count but resulted in a greater exacerbation frequency in those with a low blood eosinophil count. This finding contrasts with that for asthma for which absence of eosinophilic inflammation is associated with neither benefit nor harm to anti‒IL-5(R). Interestingly, the airway microbiome is distinct between COPD patients with vs those without eosinophilic inflammation. Corticosteroid therapy alters the airway microbiome and consequently might hinder recovery during exacerbations in patients without eosinophilic inflammation. Whether this exacerbation relationship to low eosinophil count is genuine and these effects are partly because of attenuation of Correspondence: Christopher E Brightling University of Leicester, Glenfield General Hospital, Leicester, LE3 9QP, UK Tel +44 116 258 3998 Fax +44 116 25

[1]  I. Pavord,et al.  Mepolizumab for Eosinophilic Chronic Obstructive Pulmonary Disease , 2017, The New England journal of medicine.

[2]  James R. Brown,et al.  Lung microbiome dynamics in COPD exacerbations , 2016, European Respiratory Journal.

[3]  A. Chang,et al.  Haemophilus influenzae: using comparative genomics to accurately identify a highly recombinogenic human pathogen , 2015, BMC Genomics.

[4]  E. Bleecker,et al.  Benralizumab for chronic obstructive pulmonary disease and sputum eosinophilia: a randomised, double-blind, placebo-controlled, phase 2a study. , 2014, The Lancet. Respiratory medicine.

[5]  Christopher E Brightling,et al.  Blood eosinophils to direct corticosteroid treatment of exacerbations of chronic obstructive pulmonary disease: a randomized placebo-controlled trial. , 2012, American journal of respiratory and critical care medicine.

[6]  K. Riesbeck,et al.  Nontypeable Haemophilus influenzae activates human eosinophils through beta-glucan receptors. , 2003, American journal of respiratory cell and molecular biology.

[7]  D. Nadal,et al.  Quantitative Detection of Moraxella catarrhalis in Nasopharyngeal Secretions by Real-Time PCR , 2003, Journal of Clinical Microbiology.

[8]  Neil Hunter,et al.  Determination of bacterial load by real-time PCR using a broad-range (universal) probe and primers set. , 2002, Microbiology.

[9]  D. Nadal,et al.  Quantitative Detection of Streptococcus pneumoniae in Nasopharyngeal Secretions by Real-Time PCR , 2001, Journal of Clinical Microbiology.

[10]  I. Pavord,et al.  Sputum eosinophilia and short-term response to prednisolone in chronic obstructive pulmonary disease: a randomised controlled trial , 2000, The Lancet.

[11]  M. Yazdanbakhsh,et al.  Bactericidal action of eosinophils from normal human blood , 1986, Infection and immunity.