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pubmed-article:21288996pubmed:abstractTextThe 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.lld:pubmed
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pubmed-article:21288996pubmed:pagination647-54lld:pubmed
pubmed-article:21288996pubmed:dateRevised2011-10-3lld:pubmed
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pubmed-article:21288996pubmed:year2011lld:pubmed
pubmed-article:21288996pubmed:articleTitleMicroneedle vaccination with stabilized recombinant influenza virus hemagglutinin induces improved protective immunity.lld:pubmed
pubmed-article:21288996pubmed:affiliationDepartment of Microbiology and Immunology and Emory Vaccine Center, Emory University School of Medicine, 1510 Clifton Road, Atlanta, GA 30322, USA.lld:pubmed
pubmed-article:21288996pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21288996pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed