US2005048588A1PendingUtilityA1
Immunogenic cancer peptides and uses thereof
Priority: Nov 27, 2000Filed: Jul 19, 2004Published: Mar 3, 2005
Est. expiryNov 27, 2020(expired)· nominal 20-yr term from priority
G01N 33/5759G01N 33/5758A61K 38/02C07K 14/4748
49
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Claims
Abstract
This invention relates to novel general methods and compositions that provide cancer-specific or highly cancer-associated antigens useful for diagnosis and treatment of cancer.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A cancer-specific or highly cancer-associated peptide comprising the following structure:
(a) an amino acid sequence of a length from 3-1000 amino acids; (b) a net hydrophilic character; and (c) at least one glycosylatable amino acid located at a position in the amino acid sequence no further than 3 amino acids away from the amino acid adjacent to either end of the peptide, wherein for cells with normal growth patterns the amino acid is the site of glycosylation, but in cancer cells the site is missing entirely, so that the glycosylation site confers a cancer-specific or highly cancer-associated immunogenicity or marker function to the peptide.
3 . The peptide of claim 2 further defined as immunogenic.
4 . The peptide of claim 2 , wherein the glycosylatable amino acid is asparagine.
5 . The peptide of claim 2 , further comprising a plurality of deglycosylated amino acids, and wherein each deglycosylated amino acid is separated from the deglycosylated amino acid nearest to it by no more than 6 unmodified amino acids.
6 . The peptide of claim 5 further comprising:
(a) a chemical modification of at least one of the deglycosylated amino acids wherein the chemical modification confers upon the peptide an additional cancer-specific or highly cancer-associated immunogenicity than that due to glycosylation; and (b) an amino acid sequence wherein no more than 3 unmodified amino acids are located on either side of a modified amino acid or amino acid that has a glycosylation site removed.
7 . (canceled).
8 . The peptide of claim 2 , wherein the peptide is produced synthetically.
9 . The peptide of claim 2 , produced by the method of claim 1 .
10 . A composition comprising a peptide of claim 2 .
11 . An immunogenic composition capable of inducing a mammal to produce antibodies specific for an epitope on a cancer cell, wherein the immunogenic composition comprises a peptide of claim 2 .
12 - 23 . (canceled)
24 . A therapeutic construct comprising a peptide of claim 2 and
(a) adjuvant/peptide conjugates comprising the peptide coupled to molecule which facilitates enhanced immunogenicity; and (b) neomolecules created by recombinant techniques containing a peptide with adjuvant molecular sequences which promote increased immunogenicity of the peptide of claim 2 .
25 - 26 . (canceled)
27 . The peptide of claim 2 having a sequence selected from the group consisting of:
uNu
uNuu
Nuuu
uNuuu
uuNuu
uuNuuu
uuuNuuu
uNu M uuu
uuNu M uuu
uuuNu M uuu
uuuN MM uuu
uuuNu MM uuu
uuuN MMM uuu
uNuu M uu
uNuu M uuu
uuNuu M uuu
uuuNuu M uuu
uuNuu M uuNuu
uuuNuu M uuNuuu
uuu M uuNuu M uuu
[uuNuuN]n
[uuuNuuuN]n
[uuuNuuuuN]n
[uuuNuuuuuN]n
[uuuNuuuuuN]n
[uuuNuuuuuuN]n
[uuuNuuuuuuNu]n
[uuuNuuuuuuNuu]n
[uuuNuuuuuuNuuu]n
[uu M uuN]n
wherein u is an unmodified amino acid, N is a deglycosylated amino acid, and M is a modified amino acid.Join the waitlist — get patent alerts
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