Source:http://linkedlifedata.com/resource/pubmed/id/21288996
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2011-4-8
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pubmed:abstractText |
The emergence of the swine-origin 2009 influenza pandemic illustrates the need for improved vaccine production and delivery strategies. Skin-based immunization represents an attractive alternative to traditional hypodermic needle vaccination routes. Microneedles (MNs) can deliver vaccine to the epidermis and dermis, which are rich in antigen-presenting cells (APC) such as Langerhans cells and dermal dendritic cells. Previous studies using coated or dissolvable microneedles emphasized the use of inactivated influenza virus or virus-like particles as skin-based vaccines. However, most currently available influenza vaccines consist of solubilized viral protein antigens. Here we test the hypothesis that a recombinant subunit influenza vaccine can be delivered to the skin by coated microneedles and can induce protective immunity. We found that mice vaccinated via MN delivery with a stabilized recombinant trimeric soluble hemagglutinin (sHA) derived from A/Aichi/2/68 (H3) virus had significantly higher immune responses than did mice vaccinated with unmodified sHA. These mice were fully protected against a lethal challenge with influenza virus. Analysis of postchallenge lung titers showed that MN-immunized mice had completely cleared the virus from their lungs, in contrast to mice given the same vaccine by a standard subcutaneous route. In addition, we observed a higher ratio of antigen-specific Th1 cells in trimeric sHA-vaccinated mice and a greater mucosal antibody response. Our data therefore demonstrate the improved efficacy of a skin-based recombinant subunit influenza vaccine and emphasize the advantage of this route of vaccination for a protein subunit vaccine.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/AI074579,
http://linkedlifedata.com/resource/pubmed/grant/EB006369,
http://linkedlifedata.com/resource/pubmed/grant/R01 EB006369-01A1,
http://linkedlifedata.com/resource/pubmed/grant/R01 EB006369-02,
http://linkedlifedata.com/resource/pubmed/grant/R01 EB006369-03,
http://linkedlifedata.com/resource/pubmed/grant/R01 EB006369-04,
http://linkedlifedata.com/resource/pubmed/grant/R01 EB006369-05,
http://linkedlifedata.com/resource/pubmed/grant/U01 EB012495-01
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1556-679X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
647-54
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pubmed:dateRevised |
2011-10-3
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pubmed:meshHeading |
pubmed-meshheading:21288996-Animals,
pubmed-meshheading:21288996-Disease Models, Animal,
pubmed-meshheading:21288996-Hemagglutinin Glycoproteins, Influenza Virus,
pubmed-meshheading:21288996-Immunity, Mucosal,
pubmed-meshheading:21288996-Influenza A virus,
pubmed-meshheading:21288996-Influenza Vaccines,
pubmed-meshheading:21288996-Injections, Intradermal,
pubmed-meshheading:21288996-Lung,
pubmed-meshheading:21288996-Mice,
pubmed-meshheading:21288996-Mice, Inbred BALB C,
pubmed-meshheading:21288996-Orthomyxoviridae Infections,
pubmed-meshheading:21288996-Survival Analysis,
pubmed-meshheading:21288996-Th1 Cells,
pubmed-meshheading:21288996-Vaccination,
pubmed-meshheading:21288996-Vaccines, Subunit,
pubmed-meshheading:21288996-Vaccines, Synthetic,
pubmed-meshheading:21288996-Viral Load
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pubmed:year |
2011
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pubmed:articleTitle |
Microneedle vaccination with stabilized recombinant influenza virus hemagglutinin induces improved protective immunity.
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pubmed:affiliation |
Department of Microbiology and Immunology and Emory Vaccine Center, Emory University School of Medicine, 1510 Clifton Road, Atlanta, GA 30322, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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