| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Previous Article | Next Article ![]()
Clinical and Vaccine Immunology, July 2007, p. 926-928, Vol. 14, No. 7
1071-412X/07/$08.00+0 doi:10.1128/CVI.00450-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Mary Hoelscher,1,
Jessica A. Belser,1
Chong Wang,1
Lakshmi Jayashankar,1
Zhu Guo,1
Ross H. Durland,2
Jacqueline M. Katz,1 and
Suryaprakash Sambhara1*
Influenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia 30333,1 Altea Therapeutics, Tucker, Georgia 300842
Received 20 November 2006/ Returned for modification 9 March 2007/ Accepted 30 April 2007
In the event of another influenza virus pandemic, strategies for effective mass vaccination will urgently be needed. We used a novel transdermal patch delivery technology, known as the PassPort system, to vaccinate mice with recombinant H5 hemagglutinin with or without immunomodulators. This needle-free form of vaccine delivery induced robust serum antibody responses that were augmented by different immunomodulators that stimulated the innate immune system and protected mice against lethal challenge with a highly pathogenic avian H5N1 influenza virus.
Published ahead of print on 9 May 2007.
S.G. and M.H. contributed equally to the present study.
| Antimicrob. Agents Chemother. | Clin. Microbiol. Rev. | Infect. Immun. |
|---|---|---|
| J. Clin. Microbiol. | J. Virol. | ALL ASM JOURNALS |