US2007218073A1PendingUtilityA1
Antigenic composition
Est. expiryJun 8, 2020(expired)· nominal 20-yr term from priority
A61K 2039/55561C12N 15/117C07H 19/24A61K 39/39A61K 2039/55516A61K 38/00C12N 2310/33C12N 2310/315A61P 37/04C12N 2310/18A61P 37/00
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Claims
Abstract
The invention relates to a composition comprising a T cell epitope or a mixture of T cell epitopes a polycationic peptide and a nucleic acid based on inosin and cytosin and its use as a vaccine.
Claims
exact text as granted — not AI-modified1 - 15 . (canceled)
16 . A pharmaceutical composition comprising
at least one T cell epitope, said T cell epitope further defined as a peptide of 6 to 20 amino acid residues, or a mixture of such T cell epitopes; a polycationic peptide; and a nucleic acid based on inosine and cytosine.
17 . The composition of claim 16 , wherein the nucleic acid based on inosine and cytosine is poly I: poly C, poly IC, poly dC: poly dI, or poly dIC.
18 . The composition of claim 16 , wherein the polycationic peptide is polyarginine, polylysine, or a polypeptide containing at least 50% basic amino acid residues.
19 . The composition of claim 18 , wherein the polycationic peptide is a polypeptide containing least 50% arginine residues, lysine residues, or a combination of arginine and lysine residues.
20 . The composition of claim 16 , wherein the polycationic peptide contains more than 5 residues.
21 . The composition of claim 20 , wherein the polycationic peptide contains between 10 and 1000 residues.
22 . The composition of claim 21 , wherein the polycationic peptide contains between 50 and 500 residues.
23 . The composition of claim 16 , wherein the T cell epitope is derived from a human, animal or plant pathogen.
24 . The composition of claim 16 , wherein the T cell epitope is derived from a viral or bacterial pathogen.
25 . The composition of claim 16 , wherein the T cell epitope is derived from a parasite or plant pathogen.
26 . The composition of claim 16 , wherein the T cell epitope is further defined as a glycosylated peptide and/or a lipidated peptide.
27 . The composition of claim 26 , wherein the T cell epitope is further defined as a peptide of 7 to 15 amino acid residues.
28 . The composition of claim 27 , wherein the T cell epitope is further defined as a peptide of 8 to 11 amino acid residues.
29 . The composition of claim 16 , further defined as comprising:
from 1 ng to 1 g T cell epitope; from 1 ng to 1 g polycationic peptide; and from 1 ng to 1 g nucleic acid based on inosine and cytosine.
30 . The composition of claim 29 , further defined as comprising from 1 to 10000 μg T cell epitope.
31 . The composition of claim 29 , further defined as comprising from 0.1 to 1000 μg polycationic peptide.
32 . The composition of claim 29 , further defined as comprising from 10 μg to 300 mg nucleic acid based on inosine and cytosine.
33 . The composition of claim 16 , further comprising at least one auxiliary substance or further effective substance.
34 . The composition of claim 16 , further defined as a vaccine.
35 . A method of inducing a systemic immune response comprising:
obtaining a pharmaceutical composition comprising: at least one T cell epitope, said T cell epitope further defined as a peptide of 6 to 20 amino acid residues, or a mixture of such T cell epitopes; a polycationic peptide; and a nucleic acid based on inosine and cytosine; and administering the pharmaceutical composition to a patient.
36 . A kit for vaccination comprising:
a component containing at least one T cell epitope, said T cell epitope further defined as a peptide of 6 to 20 amino acid residues, or a mixture of such T cell epitopes; a polycationic peptide; and a nucleic acid based on inosine and cytosine.
37 . A method of eliciting an epitope specific T cell response comprising:
obtaining a pharmaceutical composition comprising a polycationic peptide and a nucleic acid based on inosine and cytosine; and administering the pharmaceutical composition to a patient.Cited by (0)
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