Title

IL-10 delivery by AAV5 vector attenuates inflammation in mice with Pseudomonas pneumonia

UMMS Affiliation

Department of Pediatrics

Date

5-2-2010

Document Type

Article

Medical Subject Headings

Animals; Cystic Fibrosis; Dependovirus; Gene Therapy; Genetic Vectors; Interleukin-10; Intubation, Intratracheal; Mice; Mice, Knockout; Neutrophils; Pneumonia, Bacterial; Pseudomonas Infections; *Pseudomonas aeruginosa

Disciplines

Allergy and Immunology | Digestive System Diseases | Genetics and Genomics | Pediatrics

Abstract

Lung infections with Pseudomonas aeruginosa and other pathogens in cystic fibrosis (CF) cause progressive airway obstruction and tissue damage, the predominant cause of morbidity and mortality in CF. We investigated whether a recombinant adeno-associated virus type 5 (AAV5) vector expressing murine interleukin (IL)-10 (AAV5.Cbeta-mIL-10), a regulatory/anti-inflammatory cytokine, could decrease airway inflammation in IL-10 knockout mice chronically infected with mucoid P. aeruginosa. Mice that received AAV5.Cbeta-mIL10 through intratracheal inoculation produced IL-10 at an average of 25 000 pg/ml in the epithelial lining fluid (ELF) and 12 000 pg/g-lung tissue 6 weeks post-vector delivery, significantly higher levels than in placebo-treated mice. At 3 days post-infection, proinflammatory cytokines (IL-1beta, tumor necrosis factor (TNF)-alpha, macrophage inhibitory protein (MIP)-1alpha and (KC) in the ELF and lung homogenate were decreased (1-9 folds) in the AAV5.Cbeta-mIL10-treated mice accompanied by less pronounced and more localized neutrophil infiltration in lung sections, when compared with placebo-treated mice. These results suggest that AAV5.Cbeta-mIL10 induces IL-10 levels in the lungs mediating a significant anti-inflammatory response and making AAV-IL-10 gene transfer a potentially useful therapy in the treatment of CF lung disease.

Rights and Permissions

Citation: Gene Ther. 2010 May;17(5):567-76. Epub 2010 Apr 1. Link to article on publisher's site

Related Resources

Link to Article in PubMed

PubMed ID

20357828