US2008095800A1PendingUtilityA1
Eliciting HCV-specific antibodies
Assignee: NOVARTIS VACCINES & DIAGNOSTICPriority: Dec 1, 1999Filed: Dec 13, 2007Published: Apr 24, 2008
Est. expiryDec 1, 2019(expired)· nominal 20-yr term from priority
A61P 31/12A61P 31/14A61P 37/04A61P 31/00A61P 1/16A61K 9/167A61K 2039/53C12N 2770/24234C07K 14/005A61K 2039/55555A61K 31/7088A61K 2039/57A61K 39/29A61K 2039/55511C12N 2770/24222A61K 2039/55566A61K 39/12
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Claims
Abstract
Described herein is a method of eliciting antibodies and neutralizing of binding antibodies against a hepatitis C virus (HCV) E1E2 or E2 antigen using HCV E2 or HCV E1E2 polypeptides and/or HCV E2 or E1E2 polynucleotides. Elicitation of anti-E2 antibodies and anti-E2 NOB antibodies can be used, inter alia, to provide model systems to optimize anti-E2 antibody responses and/or anti-E2 NOB antibody responses to HCV and to provide prophylactic or therapeutic treatment against HCV infection.
Claims
exact text as granted — not AI-modified1 . A composition comprising an E1E2 polypeptide, a pharmaceutically: acceptable vehicle and an adjuvant, wherein said E1E2 polypeptide is expressed from a polynucleotide encoding amino acids 192-809 of the HCV polyprotein, numbered relative to the HCV-1 polyprotein.
2 . The composition of claim 1 , wherein the adjuvant is a submicron oil-in-water emulsion.
3 . The composition of claim 1 , wherein the submicron oil-in-water emulsion is MF-59.
4 . A method of eliciting an immune response against a hepatitis C virus (HCV) envelope antigen in a vertebrate subject, said method comprising administering the composition of claim 1 to said subject.
5 . A method of eliciting an immune response against a hepatitis C virus (HCV) envelope antigen in a vertebrate subject, said method comprising administering the composition of claim 2 to said subject.
6 . A method of eliciting an immune response against a hepatitis C virus (HCV) envelope antigen in a vertebrate subject, said method comprising administering the composition of claim 3 to said subject.
7 . The method of claim 4 , wherein the immune response is a humoral immune response.
8 . The method of claim 4 , wherein the subject is infected with an HCV.
9 . The method of claim 4 , wherein the subject is not infected with an HCV.
10 . The method of claim 4 , wherein the subject is a mammal.
11 . The method of claim 10 , wherein the mammal is selected from the group consisting of a mouse, a rabbit, a guinea pig, a macaque, a baboon, a chimpanzee, and a human.
12 . The method of claim 4 , wherein the polynucleotide is administered by a method selected from the group consisting of intramuscular, subcutaneous, intraperitoneal, intranasal, oral, and intradermal administration.Join the waitlist — get patent alerts
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