US2011070298A1PendingUtilityA1
Compositions Comprising Liposomes, An Antigen, A Polynucleotide and A Carrier Comprising a Continuous Phase of a Hydrophobic Substance
Assignee: IMMUNOVACCINE TECHNOLOGIES INCPriority: Jun 5, 2008Filed: May 22, 2009Published: Mar 24, 2011
Est. expiryJun 5, 2028(~1.8 yrs left)· nominal 20-yr term from priority
Inventors:Marc MansourLeeladhar SammaturLisa Diana MacdonaldMohan KarkadaGenevieve Mary WeirAntar Fuentes-Ortega
A61K 39/0007A61K 39/39A61K 2039/55555A61K 39/12C12N 2710/20034A61P 31/20A61K 2039/55561A61K 9/127C12N 2760/16134A61P 35/00A61K 9/10A61K 2039/55544A61K 31/785A61K 2039/55505A61P 25/28A61K 2039/55566A61K 47/06A61K 2039/575A61K 9/19A61K 9/107A61P 31/16A61K 39/00Y02A50/30
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Claims
Abstract
The invention provides a composition comprising: an antigen; liposomes; a polyI:C polynucleotide; and a carrier comprising a continuous phase of a hydrophobic substance. Methods for making and using the compositions are also provided.
Claims
exact text as granted — not AI-modified1 . A composition comprising:
(a) an antigen; (b) liposomes; (c) a polyI:C polynucleotide; and (d) a carrier comprising a continuous phase of a hydrophobic substance.
2 . The composition according to claim 1 , wherein the polyI:C polynucleotide comprises RNA or DNA.
3 . The composition according to claim 1 , wherein the polyI:C polynucleotide comprises RNA and DNA.
4 . The composition according to claim 1 , wherein the polyI:C polynucleotide is a homopolymer or a heteropolymer.
5 . The composition according to claim 1 , wherein the polyI:C polynucleotide comprises a homopolymeric polyI:C polynucleotide and a heteropolymeric polyI:C polynucleotide.
6 . A method for making a composition, said method comprising combining, in any order:
a) an antigen; (b) liposomes; (c) a polyI:C polynucleotide; and (d) a carrier comprising a continuous phase of a hydrophobic substance.
7 . The method according to claim 6 , wherein said antigen is encapsulated in said liposomes.
8 . The method according to claim 6 , wherein said polyI:C polynucleotide is encapsulated in said liposomes.
9 . The method according to claim 6 , wherein said polyI:C polynucleotide is added outside said liposomes.
10 . A composition prepared according to the method of claim 6 .
11 . A method comprising administering the composition according to claim 1 to a subject in need thereof.
12 . The method according to claim 11 , which is a method for inducing an antibody response and/or cell-mediated immune response to said antigen in said subject.
13 . The method according to claim 11 , which is a method for the treatment and/or prevention of a disease caused by a bacteria, a virus, a fungus, a parasite, an allergen or a tumor cell that expresses the antigen.
14 . The method according to claim 13 , wherein the treatment and/or prevention comprises inducing an antibody and/or a cell mediated immune response to the antigen in the subject, wherein the subject has or is at risk of developing a viral infection.
15 . The method according to claim 14 , wherein the viral infection is an influenza virus infection.
16 . The method according to claim 13 , wherein the treatment and/or prevention comprises inducing an antibody and/or a cell mediated immune response to the antigen in the subject, wherein the subject has or is at risk of developing cancer.
17 . The method according to claim 11 , which is a method for the treatment and/or prevention of a neurodegenerative disease, wherein the neurodegenerative disease is associated with expression of the antigen.
18 . The method according to claim 17 , wherein the neurodegenerative disease is Alzheimer's disease.
19 . The method according to claim 11 , wherein the composition induces an immune response in the subject that is at least 1.5× higher relative to a response induced by a control composition.
20 . The method according to claim 19 , wherein the composition induces an immune response in the subject that is at least 5× higher relative to a response induced by a control composition.
21 . The method according to claim 11 , wherein the composition is administered via a route that is nasal, oropharyngeal, ocular, oral, rectal, sublingual, genitourinary mucosa, intranasal, oropharyngeal, intratracheal, intrapulmonary, transdermal, transpulmonary, intraarterial, intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous or submucosal.Join the waitlist — get patent alerts
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