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Research Paper

Vaxfectin™-Formulated Influenza DNA Vaccines Encoding NP and M2 Viral Proteins Protect Mice against Lethal Viral Challenge

Gretchen S. Jimenez, Rodrick Planchon, Qun Wei, Denis Rusalov, Andrew Geall, Joel Enas, Peggy Lalor, Vicky Leamy, Ruth Vahle, Catherine J. Luke, Alain Rolland, David C. Kaslow and Larry R. Smith

volume 3 | issue 5

september/october 2007
Pages: 157 - 164

This is an open-access article

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Next generation influenza vaccines containing conserved antigens may enhance immunity against seasonal or pandemic influenza virus strains. Using a plasmid DNA (pDNA)-based vaccine approach, we systematically tested combinations of NP, M1, and M2 antigens derived from consensus sequences for protection against lethal influenza challenge and compared formulations for adjuvanting low pDNA vaccine doses. The highest level of protection at the lowest pDNA doses was provided by Vaxfectin™-formulated NP + M2. Vaxfectin™ adjuvanticity was confirmed with a low dose of HA pDNA. These promising proof-of-concept data support the clinical development of Vaxfectin™-formulated pDNA encoding NP + M2 consensus proteins.

Authors

Gretchen S. Jimenez

Vical Incorporated, San Diego, CA

Rodrick Planchon

Vical Incorporated, San Diego, CA

Qun Wei

Vical Incorporated, San Diego, CA

Denis Rusalov

Vical Incorporated, San Diego, CA

Andrew Geall

Vical Incorporated, San Diego, CA

Joel Enas

Vical Incorporated, San Diego, CA

Peggy Lalor

Vical Incorporated, San Diego, CA

Vicky Leamy

Vical Incorporated, San Diego, CA

Ruth Vahle

Vical Incorporated, San Diego, CA

Catherine J. Luke

National Institutes of Health, Bethesda, MD

Alain Rolland

Vical Incorporated, San Diego, CA

David C. Kaslow

Vical Incorporated; San Diego CA, USA

Larry R. Smith

Vical Incorporated, San Diego, CA


This is an open-access article

 Download PDF

If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.