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Mol Cells ; 12(1): 50-6, 2001 Aug 31.
Article in English | MEDLINE | ID: mdl-11561730

ABSTRACT

Respiratory syncytial virus (RSV) is one of the principal agents of bronchiolitis and pneumonia in young children. Thus, there is a strong need to make a safe and effective vaccine against the RSV infection. DNA immunization is very effective at inducing both cellular and humoral immune responses. In this study, we inserted the RSV-F gene into expression vectors, pcDNA3.1 and pQE. These constructs were transformed into C2C12 and E. coli M15 cells, respectively. The expression of the RSV-F protein was confirmed by SDS-PAGE, followed by Western blot analyses. The immunization of pcDNA3.1-RSV-F elicited both anti-RSV-F titer in mouse sera and CTL activities with mouse splenocytes. Especially, the co-administration of IL-4, or the GM-CSF gene with the RSV-F gene construct, enhanced the production of anti-RSV-F Ab. However, this enhancement disappeared by the simultaneous injection of the Th1 and Th2 type cytokine genes. The CTL activities were affected by the co-delivery of the IFN-gamma gene, but not by Th2-type cytokines.


Subject(s)
Respiratory Syncytial Virus Vaccines/immunology , Respiratory Syncytial Virus, Human/genetics , Respiratory Syncytial Virus, Human/immunology , Vaccines, DNA/immunology , Viral Proteins/immunology , Aged , Animals , Antibody Formation/immunology , Cell Line , Child , Cytotoxicity Tests, Immunologic , Granulocyte-Macrophage Colony-Stimulating Factor/genetics , Granulocyte-Macrophage Colony-Stimulating Factor/metabolism , Humans , Interferon-gamma/genetics , Interferon-gamma/metabolism , Interleukin-4/genetics , Interleukin-4/metabolism , Mice , Mice, Inbred BALB C , Microscopy, Electron, Scanning , Plasmids/genetics , Plasmids/metabolism , Vaccination , Vaccines, DNA/pharmacology , Viral Proteins/genetics
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