T-cell antigen peptide from allergen for stimulation of il-10 production
Abstract
A first or second polypeptide for use in a method of treating or preventing a disorder by tolerisation, wherein said method comprises administration of the first and second polypeptide; and wherein both first and second polypeptides: i) are of 7 to 30 amino acids in length; ii) comprise at least one MHC Class II-binding T cell epitope; and iii) are a fragment of a protein allergen or a homologous variant of said fragment; wherein said first polypeptide induces the release of an amount of IL-10 that is greater than the amount of IL-10 released in response to the whole protein allergen from which the first polypeptide derives; wherein said disorder is characterised by an inappropriate immune response to the protein allergen from which the second polypeptide derives.
Claims
exact text as granted — not AI-modified1 . A method of treating ragweed allergy comprising administering to a subject in need thereof a therapeutically effective amount of a polypeptide which:
(i) consists of the sequence of KGEAAIKLTSSAGVLSKK (SEQ ID NO: 20; RGW07D); or (ii) is a longer peptide of up to 30 amino acids in length comprising the sequence of RGW07D; (iii) is a variant of RGW07D having at least 90% homology thereto; (iv) is a variant of RGW07D comprising one or two amino acid substitutions; or (v) is a fragment of RGW07D derived by removal of one or two amino acids from the N- or C-terminal ends thereof, or by removal of one amino acid from the N-terminal end thereof and one amino acid from the C-terminal end thereof.
2 . The method of claim 1 , wherein the polypeptide is administered sequentially or in combination with a second polypeptide.
3 . The method of claim 2 , wherein said first polypeptide is administered in a composition comprising said first polypeptide and said second polypeptide.
4 . The method of claim 2 , wherein the composition comprises a pharmaceutically acceptable carrier or diluent.
5 . The method of claim 4 , wherein said composition is provided as an injectable solution, suspension or emulsion.
6 . The method of claim 4 , wherein said composition is formulated for administration parenterally, subcutaneously, intradermally or transdermally.
7 . The method of claim 1 , wherein said subject is a human.
8 . The method of claim 1 , wherein said subject is ragweed allergic.
9 . A composition comprising a polypeptide which:
(i) consists of the sequence of KGEAAIKLTSSAGVLSKK (SEQ ID NO: 20; RGW07D); or (ii) is a longer peptide of up to 30 amino acids in length comprising the sequence of RGW07D; (iii) is a variant of RGW07D having at least 90% homology thereto; (iv) is a variant of RGW07D comprising one or two amino acid substitutions; or (v) is a fragment of RGW07D derived by removal of one or two amino acids from the N- or C-terminal ends thereof, or by removal of one amino acid from the N-terminal end thereof and one amino acid from the C-terminal end thereof.
10 . The composition of claim 9 , which comprises a pharmaceutically acceptable carrier or diluent.
11 . The composition of claim 9 , which is provided as an injectable solution, suspension or emulsion.
12 . The composition of claim 9 , which is formulated for administration parenterally, subcutaneously, intradermally or transdermally.
13 . A polypeptide which:
(i) consists of the sequence of KGEAAIKLTSSAGVLSKK (SEQ ID NO: 20; RGW07D); (ii) is a longer peptide of up to 30 amino acids in length comprising the sequence of RGW07D; (iii) is a variant of RGW07D having at least 90% homology thereto; (iv) is a variant of RGW07D comprising one or two amino acid substitutions; or is a fragment of RGW07D derived by removal of one or two amino acids from the N- or C-terminal ends thereof, or by removal of one amino acid from the N-terminal end thereof and one amino acid from the C-terminal end thereof.Cited by (0)
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