Source:http://linkedlifedata.com/resource/pubmed/id/16941345
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2006-8-30
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pubmed:abstractText |
For the production of dengue-vaccine candidates, empty capsids, or virus-like particles (VLPs), of parvovirus B19 that carry dengue 2-specific epitopes were employed as antigen carriers. Two epitopes (comprising amino acids 352-368 and 386-397) of domain BIII of the envelope glycoprotein were chosen to produce recombinant B19 VLPs for immunization of BALB/c mice. Serum samples from immunized mice revealed that recombinant B19 VLPs elicited strong humoral immune responses. In summary, this B19 VLP-vaccine platform produced high (> or =2.0 x 10(5)) anti-dengue 2 titers and robust (< or =1 120) 50%-plaque-reduction neutralization test (PRNT(50)) titers, which effectively neutralized live dengue 2 virus in PRNT(50) assays.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0022-1899
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
194
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
790-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16941345-Animals,
pubmed-meshheading:16941345-Antibodies, Viral,
pubmed-meshheading:16941345-Antigen Presentation,
pubmed-meshheading:16941345-Capsid Proteins,
pubmed-meshheading:16941345-Cell Line,
pubmed-meshheading:16941345-Dengue Virus,
pubmed-meshheading:16941345-Epitopes,
pubmed-meshheading:16941345-Gene Order,
pubmed-meshheading:16941345-Mice,
pubmed-meshheading:16941345-Mice, Inbred BALB C,
pubmed-meshheading:16941345-Neutralization Tests,
pubmed-meshheading:16941345-Parvovirus B19, Human,
pubmed-meshheading:16941345-Recombinant Proteins,
pubmed-meshheading:16941345-Spodoptera
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pubmed:year |
2006
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pubmed:articleTitle |
Parvovirus B19 empty capsids as antigen carriers for presentation of antigenic determinants of dengue 2 virus.
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pubmed:affiliation |
Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA. amexis@nih.gov
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, N.I.H., Intramural
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