US2012183533A1PendingUtilityA1
Mimotopes of hiv env
Individually held — no corporate assignee on recordPriority: Oct 30, 2008Filed: Mar 30, 2011Published: Jul 19, 2012
Est. expiryOct 30, 2028(~2.3 yrs left)· nominal 20-yr term from priority
C07K 2317/24C07K 16/4216C07K 2317/76A61K 2039/55566A61K 39/12C12N 2740/16122A61K 2039/5256C12N 2795/00043C12N 2740/15022C07K 2319/00C12N 2740/16134A61P 31/18A61K 38/00A61K 39/21C07K 2317/34C07K 2318/10C07K 2317/55A61P 37/04C12N 7/00C07K 14/005A61K 2039/575C12N 2740/16171A61K 2039/53C07K 2317/21C07K 16/1145A61K 39/00
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Claims
Abstract
The invention provides methods, compositions and kits for treating and or preventing an HIV infection. For example, HIV envelope-like polypeptides (wild-type HIV polypeptides and mimotopes) may be administered to an individual so as to induce a protective immune response to HIV. Alternatively, antibodies directed to the HIV envelope-like polypeptides may be administered to an individual to treat or prevent an HIV infection and/or one or more symptoms associated with the infection (e.g., AIDS).
Claims
exact text as granted — not AI-modified1 . An isolated HIV envelope-like polypeptide, wherein said polypeptide comprises an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of those recited in FIG. 1 or FIG. 9 .
2 . The isolated HIV envelope-like polypeptide of claim 1 , wherein said polypeptide is a mimotope having an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-84.
3 . The isolated HIV envelope-like polypeptide of claim 1 , wherein said polypeptide is a mimotope of an HIV V3 envelope region and comprises an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 21, 23, 25, 28, 29 and 31.
4 . The isolated HIV envelope-like polypeptide of claim 1 , wherein said polypeptide is a mimotope of an HIV C-terminal envelope region and comprises an amino acid sequence which is 90% or more identical to the amino acid sequence selected from the group consisting of SEQ ID NOs: 34, 35, 37, 38 and 39.
5 . The isolated HIV envelope-like polypeptide of claim 1 , wherein said polypeptide is a wild-type HIV envelope polypeptide consisting essentially of an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 85-92.
6 . The isolated HIV envelope-like polypeptide of claim 3 , wherein said mimotope comprises an amino acid sequence which is 90% or more identical to the amino acid sequence of SEQ ID NO:31.
7 . The isolated HIV envelope-like polypeptide of claim 3 , wherein said polypeptide comprises the amino acid sequence of SEQ ID NO:31.
8 . The isolated HIV envelope-like polypeptide of any one of claims 1 - 7 , wherein said polypeptide is a fusion polypeptide.
9 . A composition comprising the HIV envelope-like polypeptide of any one of claims 1 - 8 and a pharmacologically acceptable carrier.
10 . A kit comprising the composition of claim 9 and instructions for use.
11 . An isolated nucleic acid encoding one or more of the HIV envelope-like polypeptides of any one of claims 1 - 8 .
12 . A vector comprising the nucleic acid molecule of claim 11 .
13 . A host cell comprising the vector of claim 12 .
14 . A composition comprising one or more of the isolated nucleic acids of claim 11 and a pharmacologically acceptable carrier.
15 . A kit comprising the composition of claim 14 , and instructions for use.
16 . A neutralizing antibody that specifically binds to an HIV C-terminal region of gp120.
17 . An antibody that specifically binds to an HIV envelope-like polypeptide, wherein said polypeptide comprises an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of those recited in FIG. 1 .
18 . The antibody of claim 17 , wherein said polypeptide is a mimotope comprising an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 1-84 or the amino acid sequences presented in FIG. 9 .
19 . The antibody of claim 17 , wherein said polypeptide is a wild-type HIV envelope polypeptide comprising an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 85-92.
20 . The antibody of claim 17 , wherein said polypeptide is a mimotope of an HIV V3 region comprising an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 21, 23, 25, 28, 29 and 31.
21 . The antibody of claim 17 , wherein said polypeptide is a mimotope of an HIV C-terminal envelope polypeptide comprising an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 34, 35, 37, 38 and 39.
22 . The antibody of claim 20 , wherein said mimotope comprises an amino acid sequence which is 90% or more identical to the amino acid sequences of SEQ ID NO:31.
23 . The antibody of claim 20 , wherein said mimotope comprises the amino acid sequence of SEQ ID NO:31.
24 . The antibody of any one of claims 17 - 23 , wherein the antibody is an HIV neutralizing antibody.
25 . The antibody of any one of claims 17 - 24 , wherein said antibody is a mouse or monkey antibody.
26 . The antibody of any one of claims 17 - 24 , wherein said antibody is a human antibody.
27 . The antibody of any one of claims 17 - 26 , wherein said antibody is a polyclonal antibody.
28 . The antibody of any one of claims 17 - 26 , wherein said antibody is a monoclonal antibody.
29 . The antibody of any one of claims 17 - 24 , wherein said antibody is a chimeric antibody.
30 . The antibody of any one of claims 17 - 24 , wherein said antibody is a humanized antibody.
31 . The antibody of any one of claims 17 - 30 wherein said antibody is a binding fragment.
32 . A composition comprising the antibody of any one of claims 17 - 31 and a pharmacologically acceptable carrier.
33 . The antibody of any one of claims 17 - 31 wherein said antibody is a Fab fragment.
34 . A kit comprising the composition of claim 32 and instructions for use.
35 . A cell line expressing the antibody of any one of claims 17 - 33 .
36 . A method for inducing an immune response in a subject comprising administering a pharmaceutical composition comprising an immunologically effective dose of an HIV envelope-like polypeptide, wherein said polypeptide comprises an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of those listed in FIG. 1 or FIG. 9 .
37 . The method of claim 36 , wherein the polypeptide is a mimotope comprising an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 1-84.
38 . The method of claim 36 , wherein the polypeptide is a wild-type HIV envelope polypeptide consisting essentially of an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 85-92.
39 . The method of claim 36 , wherein the polypeptide is an HIV V3 region mimotope comprising an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 21, 23, 25, 28, 29 and 31.
40 . The method of claim 36 , wherein the polypeptide is an HIV C-terminal envelope mimotope comprising an amino acid sequence which is 90% or more identical to the amino acid sequence selected from the group consisting of SEQ ID NO: 34, 35, 37, 38 and 39.
41 . The method of claim 39 , wherein the mimotope comprises an amino acid sequence which is 90% or more identical to the amino acid sequence of SEQ ID NO:31.
42 . The method of claim 39 , wherein the mimotope comprises the amino acid sequence of SEQ ID NO:31.
43 . The method of any one of claims 36 - 43 , further comprising administering a nucleic acid encoding an HIV envelope polypeptide.
44 . A method for treating or preventing an HIV infection in a subject, the method comprising administering a therapeutically effective dose of an antibody that specifically binds to an HIV envelope-like polypeptide comprising an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of those recited in FIG. 1 or FIG. 9 .
45 . The method of claim 44 , wherein the polypeptide is a mimotope comprising an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 1-84.
46 . The method of claim 44 , wherein the polypeptide is an HIV V3 region mimotope having an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 21, 23, 25 28, 29 and 31.
47 . The method of claim 44 , wherein the polypeptide is an HIV C-terminal envelope mimotope comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 34, 35, 37, 38 and 39.
48 . The method of claim 44 , wherein the polypeptide is a wild type HIV envelope polypeptide comprising an amino acid sequence which is 90% or more identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 85-92.
49 . The method of claim 46 , wherein the mimotope comprises an amino acid sequence which is 90% or more identical to the amino acid sequences of SEQ ID NO:31.
50 . The method of claim 46 , wherein the mimotope comprises the amino acid sequence of SEQ ID NO:31.
51 . The method of any one of claims 36 - 50 , wherein the HIV envelope-like polypeptide is coupled to a immunocarrier.
52 . An antibody produced by a hybridoma selected from the group consisting of ATCC#s:
53 . A cell line deposited as ATCC#.Join the waitlist — get patent alerts
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