Method of conferring a protective immune response to Norovirus
The present invention relates to vaccine compositions comprising Norovirus antigens and adjuvants, in particular, mixtures of monovalent VLPs and mixtures of multivalent VLPs, and to methods of conferring protective immunity to Norovirus infections in a human subject.
1. A method of eliciting protective immunity to a Norovirus infection in a human comprising administering to the human a vaccine comprising Norovirus virus-like particles (VLPs) and at least one adjuvant, wherein said Norovirus VLPs comprise Norovirus genogroup I VLPs and Norovirus genogroup II VLPs.
2. The method of claim 1 , wherein said Norovirus VLPs are monovalent VLPs.
3. The method of claim 1 , wherein said Norovirus VLPs are multivalent VLPs.
4. The method of claim 1 , wherein said Norovirus genogroup I VLPs are Norwalk virus VLPs and said Norovirus genogroup II VLPs are Houston virus VLPs.
5. The method of claim 1 , wherein said vaccine further comprises a delivery agent.
6. The method of claim 5 , wherein the delivery agent is a bioadhesive.
7. The method of claim 6 , wherein said bioadhesive is a mucoadhesive.
8. The method of claim 7 , wherein said mucoadhesive is selected from the group consisting of dermatan sulfate, chondroitin, pectin, mucin, alginate, cross-linked derivatives of poly(acrylic acid), polyvinyl alcohol, polyvinyl pyrollidone, polysaccharides, hydroxypropyl methylcellulose, lectins, fimbrial proteins, and carboxymethylcellulose.
9. The method of claim 8 , wherein said mucoadhesive is a polysaccharide.
10. The method of claim 9 , wherein said polysaccharide is chitosan, chitosan salt, or chitosan base.
11. The method of claim 1 , wherein the adjuvant is selected from the group consisting of toll-like receptor (TLR) agonists, monophosphoryl lipid A (MPL), synthetic lipid A, lipid A mimetics or analogs, aluminum salts, cytokines, saponins, muramyl dipeptide (MDP) derivatives, CpG oligos, lipopolysaccharide (LPS) of gram-negative bacteria, polyphosphazenes, emulsions, virosomes, cochleates, poly(lactide-co-glycolides) (PLG) microparticles, poloxamer particles, microparticles, and liposomes.
12. The method of claim 11 , wherein the adjuvant is a toll-like receptor (TLR) agonist.
13. The method of claim 11 , wherein the adjuvant is MPL.
14. The method of claim 1 , wherein the adjuvant is not a toxin adjuvant.
15. The method of claim 1 , wherein the vaccine is in a powder formulation.
16. The method of claim 1 , wherein the vaccine is in a liquid formulation.
17. The method of claim 1 , wherein said vaccine is administered to the human by a route selected from the group consisting of mucosal, intranasal, intramuscular, intravenous, subcutaneous, intradermal, subdermal, and transdermal routes of administration.