Enhancement of mucosal immune response against the M2eHBc+ antigen in mice with the fusion expression products of LTB and M2eHBc+ through mucosal immunization route
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Veterinary,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11259-009-9222-7.pdf
Reference32 articles.
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3. De Filette, M., Min Jou, W., Birkett, A., Lyons, K., Schultz, B., Tonkyro, A., Resch, S., and Fiers, W., 2005. Universal influenza A vaccine: Optimization of M2-based constructs. Virology, 337, 149–161 doi: 10.1016/j.virol.2005.04.004
4. De Filette, M., Ramne, A., Birkett, A., Lycke, N., Löwenadler, B., Min Jou, W., Saelens, X., and Fiers, W., 2006. The universal influenza vaccine M2e-HBc administered intranasally in combination with the adjuvant CTA1-DD provides complete protection. Vaccine, 24, 544–551
5. De Haan, L., Verweij, W.R., Holtrop, M., Brands, R., Van Scharrenburg, G.J.M., Palache, A.M., Agsteribbe, E., and Wilschut, J., 2001. Nasal or intramuscular immunization of mice with influenza subunit antigen and the B subunit of Escherichia coli heat-labile toxin induces IgA- or IgG-mediated protective mucosal immunity. Vaccine, 19, 2898–2907 doi: 10.1016/S0264-410X(00)00556-9
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