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The present invention is concerned with vaccines and their preparation. An effective long-term immune response, especially in mammals, can be produced using a vaccine comprising an antigen encapsulated in liposomes, a suitable adjuvant and a carrier comprising a continuous phase of a hydrophobic substance. The vaccine is particularly effective in eliciting the production of antibodies that recognize epitopes of native proteins.

InventorsRobert George Brown, William Pohajdak, Warwick Charles Kimmins
Original AssigneeImmunovaccine Technologies, Inc.
Primary Examiner: Nita Minnifield
Attorney: Welsh & Katz, Ltd.
Current U.S. Classification424/184.1; 424/193.1; 424/283.1; 424/450; 424/455; 424/561; 424/689; 424/690; 424/698; 424/812; 514/4.3; 514/937
International Classification: A61K/3900; A61K/3800; A61K/9127; A01N/3718; A01N/5906

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Citations

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US6670195May 26, 2000Dec 30, 2003New York UniversityMutant genes in Familial British Dementia and Familial Danish Dementia
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Referenced by

Citing PatentFiling dateIssue dateOriginal AssigneeTitle
US7344720Nov 15, 2004Mar 18, 2008Sanofi Pasteur SAVaccine composition
US7824686Nov 20, 2008Nov 2, 2010Immunovaccine Technologies, Inc.Vaccines with enhanced immune response and methods for their preparation

Claims

1. A vaccine composition, comprising:

(a) a carrier comprising a continuous phase of a hydrophobic substance;
(b) liposomes;
(c) an antigen encapsulated in said liposomes, said antigen being an antigen which, when not in said vaccine composition, has a conformation other than its native conformation, with the proviso that said antigen is other than a zona pellucida-derived antigen; and,
(d) an adjuvant.

2. The composition of claim 1, wherein the hydrophobic substance is a liquid.

3. The composition of claim 2, wherein the carrier is an oil or a water-in-oil emulsion.

4. The composition of claim 3, wherein the oil is mineral oil, a vegetable oil or a nut oil.

5. The composition of claim 3, wherein the adjuvant is alum or another compound of aluminum.

6. The composition of claim 5, wherein the adjuvant is alum.

7. The composition of claim 3, wherein the antigen is a non-native, recombinant or denatured protein, a recombinant or synthetic peptide, or a fragment thereof.

8. The composition of claim 7, wherein the antigen is a viral, bacterial, protozoal or mammalian antigen.

9. The composition of claim 8, wherein the antigen elicits an antibody that recognizes a native epitope.

10. The composition of claim 9, wherein the native epitope is a mammalian epitope.

11. The composition of claim 10, wherein the mammal is a horse, a rabbit, a deer or a cat.

12. The composition of claim 7, wherein the antigen is alcohol dehydrogenase or a hepatitis B antigen.

13. The composition of claim 3, wherein the liposomes comprise unesterified cholesterol and a phospholipid with at least one head group selected from the group consisting of phosphoglycerol, phosphoethanolamine, phosphoserine, phosphocholine and phosphoinositol.

14. The composition of claim 3 which is essentially free of lipid A.

Drawings