Efficacy of Rhesus Theta-Defensin-1 in Experimental Models of Pseudomonas aeruginosa Lung Infection and Inflammation

Author:

Bensman Timothy J.1,Jayne Jordanna G.1,Sun Meiling2,Kimura Elza3,Meinert Joshua1,Wang Joshua C.1,Schaal Justin B.4,Tran Dat4,Rao Adupa P.5,Akbari Omid6,Selsted Michael E.4,Beringer Paul M.1

Affiliation:

1. Department of Clinical Pharmacy, School of Pharmacy, University of Southern California, Los Angeles, California, USA

2. China Pharmaceutical University, Ninjin, Jiangsu, China

3. State University of Maringá, Maringá, Paraná, Brazil

4. Department of Pathology and Laboratory Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California, USA

5. Division of Pulmonary and Critical Care, Keck School of Medicine, University of Southern California, Los Angeles, California, USA

6. Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA

Abstract

ABSTRACT Chronic airway infection and inflammation contribute to the progressive loss of lung function and shortened survival of patients with cystic fibrosis (CF). Rhesus theta defensin-1 (RTD-1) is a macrocyclic host defense peptide with antimicrobial and immunomodulatory activities. Combined with favorable preclinical safety and peptide stability data, RTD-1 warrants investigation to determine its therapeutic potential for treatment of CF lung disease. We sought to evaluate the therapeutic potential of RTD-1 for CF airway infection and inflammation using in vitro , ex vivo , and in vivo models. We evaluated RTD-1's effects on basal and Pseudomonas aeruginosa- induced inflammation in CF sputum leukocytes and CF bronchial epithelial cells. Peptide stability was evaluated by incubation with CF sputum. Airway pharmacokinetics, safety, and tolerance studies were performed in naive mice. Aerosolized RTD-1 treatment effects were assessed by analyzing lung bacterial burdens and airway inflammation using an established model of chronic P. aeruginosa endobronchial infection in CF (ΔF508) mice. RTD-1 directly reduces metalloprotease activity, as well as inflammatory cytokine secretion from CF airway leukocyte and bronchial epithelial cells. Intrapulmonary safety, tolerability, and stability data support the aerosol administration route. RTD-1 reduced the bacterial lung burden, airway neutrophils, and inflammatory cytokines in CF mice with chronic P. aeruginosa lung infection. Collectively, these studies support further development of RTD-1 for treatment of CF airway disease.

Funder

Cystic Fibrosis Research, Inc.

Webb Foundation

HHS | National Institutes of Health

HHS | NIH | National Institute of General Medical Sciences

HHS | NIH | National Institute of Dental and Craniofacial Research

Cystic Fibrosis Foundation

Arthritis Foundation

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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