Nanoparticulate CpG immunotherapy in RAO-affected horses: phase I and IIa study

J Vet Intern Med. 2015 Jan;29(1):286-93. doi: 10.1111/jvim.12524.

Abstract

Background: Recurrent airway obstruction (RAO), an asthma-like disease, is 1 of the most common allergic diseases in horses in the northern hemisphere. Hypersensitivity reactions to environmental antigens cause an allergic inflammatory response in the equine airways. Cytosine-phosphate-guanosine-oligodeoxynucleotides (CpG-ODN) are known to direct the immune system toward a Th1-pathway, and away from the pro-allergic Th2-line (Th2/Th1-shift). Gelatin nanoparticles (GNPs) are biocompatible and biodegradable immunological inert drug delivery systems that protect CpG-ODN against nuclease degeneration. Preliminary studies on the inhalation of GNP-bound CpG-ODN in RAO-affected horses have shown promising results.

Objectives: The aim of this study was to evaluate the clinical and immunological effects of GNP-bound CpG-ODN in a double-blinded, placebo-controlled, prospective, randomized clinical trial and to verify a sustained effect post-treatment.

Animals and methods: Twenty-four RAO-affected horses received 1 inhalation every 2 days for 5 consecutive administrations. Horses were examined for clinical, endoscopic, cytological, and blood biochemical variables before the inhalation regimen (I), immediately afterwards (II), and 4 weeks post-treatment (III).

Results: At time points I and II, administration of treatment rather than placebo corresponded to a statistically significant decrease in respiratory effort, nasal discharge, tracheal secretion, and viscosity, AaDO2 and neutrophil percentage, and an increase in arterial oxygen pressure.

Conclusion and clinical importance: Administration of a GNP-bound CpG-ODN formulation caused a potent and persistent effect on allergic and inflammatory-induced clinical variables in RAO-affected horses. This treatment, therefore, provides an innovative, promising, and well-tolerated strategy beyond conventional symptomatic long-term therapy and could serve as a model for asthma treatment in humans.

Keywords: Gelatin nanoparticle; Immunotherapy; Inhalation; RAO.

Publication types

  • Clinical Trial, Phase I
  • Clinical Trial, Phase II
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Auscultation
  • Female
  • Horse Diseases / drug therapy*
  • Horses
  • Lung / pathology
  • Lung Diseases, Obstructive / drug therapy
  • Lung Diseases, Obstructive / veterinary*
  • Male
  • Mucus
  • Nanoparticles / adverse effects
  • Nanoparticles / therapeutic use*
  • Oligodeoxyribonucleotides / adverse effects
  • Oligodeoxyribonucleotides / therapeutic use*
  • Oxygen / blood
  • Partial Pressure
  • Respiration / drug effects

Substances

  • Oligodeoxyribonucleotides
  • Oxygen