US2006257318A1PendingUtilityA1
Method for the in vitro assessment of the progression status of an infection by an hiv virus in an individual
Assignee: ASSIST PUBL HOPITAUX DE PARISPriority: Feb 6, 2003Filed: Feb 6, 2004Published: Nov 16, 2006
Est. expiryFeb 6, 2023(expired)· nominal 20-yr term from priority
G01N 33/56988G01N 2015/1472A61P 31/18G01N 15/1459G01N 2015/1006G01N 33/505G01N 2015/1486C07K 2317/76C07K 16/28A61P 35/00C07K 2317/73C07K 16/1145G01N 15/149
45
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Claims
Abstract
The present invention relates to the field of the in vitro diagnosis nosis of the progression status of an infection of an individual with a virus belonging to the family of the Human Immunodeficiency Viruses (HIV) as well as with the therapeutical treatment of this infectious disease.
Claims
exact text as granted — not AI-modified1 .- 44 . (canceled)
45 . A polypeptide comprising the amino acid sequence:
X 1 X 2 X 3 X 4 X 5 X 6 SWSNKSX 13 X 14 X 15 X 16 X 17 ,
(SEQ ID NO: 5)
wherein X 1 , X 2 , X 3 , X 5 , X 6 , X 13 , X 15 , X 16 , and X 17 are, independently, any amino acid residue, X 4 is any amino acid residue except A and W, and X 14 is any amino acid residue except E and S.
46 . The polypeptide of claim 45 , comprising the sequence:
PWASNASWSNKSLDDIW.
(SEQ ID NO: 6)
47 . The polypeptide of claim 45 , consisting of the sequence:
PWASNASWSNKSLDDIW.
(SEQ ID NO: 6)
48 . A pharmaceutical composition comprising an effective amount of a ligand that specifically binds to a polypeptide of claim 45 and at least one physiologically acceptable excipient.
49 . The pharmaceutical composition of claim 48 , wherein the polypeptide comprises the sequence:
PWASNASWSNKSLDDIW.
(SEQ ID NO: 6)
50 . The pharmaceutical composition of claim 48 , wherein the polypeptide consists of the sequence:
PWASNASWSNKSLDDIW.
(SEQ ID NO: 6)
51 . The pharmaceutical composition of claim 48 , wherein the ligand comprises an antibody directed to the polypeptide of claim 45 .
52 . A method comprising:
incubating a candidate compound with a polypeptide of claim 45; and assaying for the binding of the candidate compound to the polypeptide.
53 . The method of claim 52 , wherein the polypeptide comprises the sequence:
PWASNASWSNKSLDDIW (SEQ ID NO: 6).
54 . The method of claim 52 , wherein the polypeptide consists of the sequence:
PWASNASWSNKSLDDIW.
(SEQ ID NO: 6)
55 . The method of claim 52 , comprising a gel migration assay to detect any complexes formed between the candidate compound and the polypeptide.Cited by (0)
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