Intranasal gene transfer by chitosan-DNA nanospheres protects BALB/c mice against acute respiratory syncytial virus infection

Hum Gene Ther. 2002 Aug 10;13(12):1415-25. doi: 10.1089/10430340260185058.

Abstract

Respiratory syncytial virus (RSV) infection is often associated in infancy with life-threatening bronchiolitis, which is also a major risk factor for the development of asthma. At present, no effective prophylaxis is available against RSV infection. Herein, we describe an effective prophylactic intranasal gene transfer strategy utilizing chitosan-DNA nanospheres (IGT), containing a cocktail of plasmid DNAs encoding all RSV antigens, except L. A single administration of IGT (25 microg/mouse) induces expression of the mRNA and proteins of all antigens in the lung and results in a significant reduction of viral titers and viral antigen load after acute RSV infection of these mice. IGT-administered mice show no significant change in airway reactivity to methacholine and no apparent pulmonary inflammation. Furthermore, IGT results in significant induction of RSV-specific IgG antibodies, nasal IgA antibodies, cytotoxic T lymphocytes, and interferon-gamma production in the lung and splenocytes compared with controls. Together, these results demonstrate the potential of IGT against acute RSV infection.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Antigens, Viral / genetics*
  • Antigens, Viral / immunology
  • Biopolymers
  • Chitin* / analogs & derivatives*
  • Chitosan
  • Drug Carriers
  • Female
  • Genetic Therapy*
  • Genetic Vectors
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism
  • Lung / immunology
  • Lung / pathology
  • Mice
  • Mice, Inbred BALB C
  • Plasmids / administration & dosage
  • Plasmids / genetics*
  • Respiratory Syncytial Virus Infections / genetics
  • Respiratory Syncytial Virus Infections / immunology
  • Respiratory Syncytial Virus Infections / pathology
  • Respiratory Syncytial Virus Infections / prevention & control*
  • Respiratory Syncytial Viruses / genetics*
  • Respiratory Syncytial Viruses / immunology
  • T-Lymphocytes, Cytotoxic / immunology
  • Vaccines, DNA / genetics
  • Vaccines, DNA / immunology
  • Viral Load
  • Viral Vaccines / genetics
  • Viral Vaccines / immunology

Substances

  • Antigens, Viral
  • Biopolymers
  • Drug Carriers
  • Vaccines, DNA
  • Viral Vaccines
  • Chitin
  • Interferon-gamma
  • Chitosan