2002
DOI: 10.1023/a:1020113902834
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Abstract: The immunity of a combined DNA vaccine of HSV-2 glycoproteins B2 (gB2) and D2 (gD2) genes in comparison to individual vaccines was studied with regard to protecting against the HSV infection. Two recombinant DNA vaccines of the pHS2-gB2 or pHS2-gD2 were constructed and formulated. The neutralizing antibody titers appeared higher in the B2 : D2 gene cocktail-vaccinated mice than that of the individual B2 or D2 gene-vaccinated group alone, and the positive KOS control induced higher titer of the neutralizing ant… Show more

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Cited by 17 publications
(4 citation statements)
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“…The vaginal external diseases were examined daily for signs of inflammation and measured mean daily lesion scores on day 1-14 following infection. The severity of the primary disease was assessed by the lesion scoring system [19,20]. The negative vaccination developed severe diseases and had no effect after 3 days, but the MEAP immunized groups were completely protected from death.…”
Section: Resultsmentioning
confidence: 99%
“…The vaginal external diseases were examined daily for signs of inflammation and measured mean daily lesion scores on day 1-14 following infection. The severity of the primary disease was assessed by the lesion scoring system [19,20]. The negative vaccination developed severe diseases and had no effect after 3 days, but the MEAP immunized groups were completely protected from death.…”
Section: Resultsmentioning
confidence: 99%
“…The vaginal external diseases were examined daily for inflammation, and the mean daily lesion scores were measured on the 1st to the 14th day following the challenge. The severity of the primary disease was assessed (1–5 scores) using the lesion scoring system [17]. The mice in all groups immunized with the five epitopes, respectively, were protected from death to a certain extent at a lethal dose, whereas the mice in the control group developed severe diseases and died, on the 3rd day after the challenge.…”
Section: Resultsmentioning
confidence: 99%
“…The antisera for the neutralization of HSV-2 (strain Sav) in vitro were assayed using the 50% plaque reduction assay [17]. The antisera were inactivated at 56°C for 30 min to inactivate the complements.…”
Section: Methodsmentioning
confidence: 99%
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