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Hum Gene Ther ; 13(12): 1415-25, 2002 Aug 10.
Article in English | MEDLINE | ID: mdl-12215263

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.


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