US2005019339A1PendingUtilityA1
Vaccines with enhanced immune response and methods for their preparation
Priority: Nov 7, 2000Filed: Aug 24, 2004Published: Jan 27, 2005
Est. expiryNov 7, 2020(expired)· nominal 20-yr term from priority
A61P 31/00A61K 39/04A61K 39/292A61K 2039/5555A61K 9/127A61K 2039/55566A61K 2039/575A61K 2039/55505A61K 2039/55555A61K 2039/545Y10S424/812A61K 39/39A61K 47/44A61K 39/12C12N 2730/10134A61P 15/00A61K 39/00
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Claims
Abstract
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.
Claims
exact text as granted — not AI-modified1 - 17 . (canceled)
18 . A method for potentiating an immune response in an animal, which method comprises administering to the animal an effective amount of 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) a suitable adjuvant.
19 . The method of claim 18 , wherein the hydrophobic substances is a liquid.
20 . The method of claim 18 , wherein the carrier is an oil or a water-in-oil emulsion.
21 . The method of claim 20 , wherein the oil is mineral oil, a vegetable oil or a nut oil.
22 . The method of claim 21 , wherein the adjuvant is alum or another compound of aluminum
23 . The method of claim 21 , wherein the antigen is alcohol dehydrogenase, or a hepatitis B antigen
24 . The method of claim 20 , wherein the antigen elicits an antibody that recognizes a native epitope.
25 . The method of claim 24 , wherein the native epitope is a mammalian epitope.
26 . The method of claim 25 , wherein the mammal is a horse, a rabbit, a deer or a cat.
27 . The method of claim 20 , wherein the composition is substantially free of lipid A.
28 - 43 . (canceled)
44 . The method of claim 22 , wherein the adjuvant is alum.
45 . The method of claim 20 , wherein the antigen is a non-native, recombinant or denatured protein, a recombinant or synthetic peptide, or a fragment thereof.
46 . The method of claim 45 , wherein the antigen is a viral, bacterial, protozoal or mammalian antigen.
47 . The method of claim 20 , 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.
48 . The method of claim 18 , wherein said vaccine composition is administered parenterally.
49 . The method of claim 18 , wherein said animal is a horse, rabbit, deer or cat.Join the waitlist — get patent alerts
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