Enhancement of DNA vaccine-induced immune responses by a 72-bp element from SV40 enhancer / 中华医学杂志(英文版)
Chin. med. j
; Chin. med. j;(24): 496-502, 2007.
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| WPRIM
| ID: wpr-344867
Biblioteca responsable:
WPRO
ABSTRACT
<p><b>BACKGROUND</b>Although DNA vaccine is considered as the next generation of vaccine, most DNA vaccine candidates are still suffering from the relatively weak immunogenicity despite the increased dosage of plasmid DNA administered. In order to enhance the immune responses elicited by a codon-optimized HIV gag DNA vaccine, a modified plasmid vector pDRVI1.0 and a booster immunization with replicating Tiantan vaccinia (RTV) strain expressing the same gene were employed.</p><p><b>METHODS</b>Vector pDRVI1.0 was constructed through inserting the 72-bp element from the SV40 enhancer, which was reported promoting nuclear transport of plasmid DNA, to the upstream of cytomegalovirus enhancer/promoter region of the plasmid vector pVR1012. Gene expression levels from expression plasmids based on pDRVI1.0 and pVR1012 were tested. Humoral and cellular immune responses induced by DNA vaccine alone or DNA prime-RTV boost regimen were determined in mice.</p><p><b>RESULTS</b>It was shown that the 72-bp element significantly enhanced the gene expression level in non-dividing cells. gag-specific humoral and cellular immune responses induced by DNA vaccination were both significantly improved, while the Th1/Th2 balance was not obviously affected by the 72-bp element. RTV boosting further significantly enhanced DNA vaccine-primed antibody and T cell responses in a Th1-biased manner.</p><p><b>CONCLUSIONS</b>The 72-bp SV40 enhancer element should be included in the DNA vaccine vector and RTV strain is a very efficient live vector for boosting immunization.</p>
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Base de datos:
WPRIM
Asunto principal:
Plásmidos
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Vaccinia
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Sangre
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Inmunoglobulina G
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Datos de Secuencia Molecular
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Anticuerpos Anti-VIH
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Productos del Gen gag
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Western Blotting
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Secuencia de Aminoácidos
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Elementos de Facilitación Genéticos
Límite:
Animals
Idioma:
En
Revista:
Chin. med. j
Año:
2007
Tipo del documento:
Article