US2003166837A1PendingUtilityA1
Isolated molecules which complex with HLA-Cw*16 molecules, and uses thereof
Priority: Sep 13, 1996Filed: May 23, 2002Published: Sep 4, 2003
Est. expirySep 13, 2016(expired)· nominal 20-yr term from priority
A61P 37/04C07K 14/4748A61P 35/00A61P 43/00A61K 38/00C07K 7/00
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Claims
Abstract
The invention involves the identification of peptides which complex with HLA-Cw*16 molecules, and which may then provoke lysis of the cells to which they bind, by cytolytic T cells. Diagnostic and therapeutic uses are described.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . Isolated peptide consisting of amino acid sequence
Xaa Ile (Xaa) 4 Arg (Xaa) 2 Tyr Xaa wherein the first Xaa is from 0-3 amino acids in length, the fourth Xaa is 0-2 amino acids in length, and the first and fourth Xaa are no more than 3 amino acids in total, each Xaa is any amino acid, and said peptide binds to an HLA-Cw16 molecule.
2 . The isolated peptide of claim 1 consisting of amino acid sequence
Ile (Xaa) 4 Arg (Xaa) 2 Tyr.
3 . The isolated peptide of claim 1 , of formula
Ile (Xaa) 4 Arg (Xaa) 2 Tyr wherein the second Xaa in (Xaa) 4 is Gly.
4 . The isolated peptide of claim 1 , of formula
Ile (Xaa) 4 Arg (Xaa) 2 Tyr wherein the fourth Xaa in (Xaa) 4 is pro.
5 . The isolated peptide of claim 1 , of formula:
Ile Xaa Gly Xaa Pro Arg (Xaa) 2 ) Tyr.
6 . The isolated peptide of claim 2 , wherein said peptide is
Ile Ser Gly Gly Pro Arg Ile Ser Tyr.
7 . The isolated peptide of claim 1 , wherein said peptide is:
Lys Ile Ser Gly Gly Pro Arg Ile Ser Tyr Pro Leu.
8 . The isolated peptide of claim 1 , wherein said peptide is
Lys Ile Ser Gly Gly Pro Arg Ile Ser Tyr.
9 . The isolated peptide of claim 1 , wherein said HLA-Cw16 molecule is HLA-Cw*1601.
10 . Method for provoking proliferation of a cytolytic T cell specific for a complex of a peptide and an HLA-Cw16 molecule, comprising contacting a T cell containing sample with a cell which present complexes of an HLA-Cw16 molecule and the peptide of claim 1 on its surface, under conditions favoring recognition of said complex by a T cell, followed by proliferation.
11 . The method of claim 10 , wherein said cell is a naturally occurring human cell.
12 . The method of claim 11 , wherein said cell is a cancer cell.
13 . The method of claim 10 , wherein said cell is a cell which has been transformed or transfected with a nucleic acid molecule which encodes an HLA-Cw16 molecule.
14 . The method of claim 10 , wherein said cell is a cell which has been transformed or transfected with a nucleic acid molecule which encodes at least a portion of MAGE-6 tumor rejection antigen precursor, said portion encoding at least a peptide of formula:
Xaa Ile (Xaa) 4 Arg (Xaa) 2 Tyr Xaa wherein the first Xaa is from 0 to 3 amino acids in length, the fourth Xaa is from 0-2 amino acids in length, each Xaa is any amino acid and the first and fourth Xaa are no more than 3 amino acids in total.
15 . Isolated nucleic acid molecule consisting of nucleotides 1033 through 1104 of cDNA for MAGE-6.
16 . Expression vector comprising the isolated nucleic acid molecule of claim 15 , operably linked to a promoter.
17 . Cell line or cell strain, transformed or transfected with the expression vector of claim 16.Join the waitlist — get patent alerts
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