Mutant CTAI fusion protein for treatment of allergy and autoimmune disease
The present invention provides improved methods and compositions for treating and preventing autoimmune and allergic diseases. More specifically, the invention relates to new immunomodulating complexes that are fusion proteins comprising a mutant subunit of the A1-subunit of the cholera toxin (CTA1), a peptide capable of binding to a specific cellular receptor, and one or more epitopes associated with an autoimmune or allergic disease. In the mutant CTA1 subunit, the amino acids corresponding to the amino acid 7, arginine, and amino acid 187, cysteine, in the native CTA1 have been replaced.
1. An immunomodulating complex being a fusion protein comprising:
(a) a mutant subunit of the ADP-ribosylating A1-subunit of the cholera toxin (CTA1) that is the that is the K-CTA1-R7K/C187A mutant having the amino acid sequence of SEQ ID NO:2,
(b) a peptide capable of binding to a specific cellular receptor, wherein said peptide is a dimer of a Protein A D-subunit; and
(c) one or more epitopes associated with an autoimmune disease, wherein, the one or more epitopes are autoimmune epitopes associated with an autoimmune disease, and
wherein the autoimmune disease is selected from the group consisting of insulin-dependent diabetes mellitus, multiple sclerosis, rheumatoid arthritis, autoimmune uveitis, primary biliary cirrhosis, myasthenia gravis, Sjögren's syndrome, pemphigus vulgaris, scleroderma, systemic lupus erythematosus, and Grave's disease.
2. The immunomodulating complexes K-CTA1-R7K/C187A-COL-DD (SEQ ID NO:4), CTA1-R7K/C187A-COL-DD (SEQ ID NO:10), K-CTA1-R7K/C187A-Ro169-DD (SEQ ID NO:11), K-CTA1-R7K/C187A-Ro211-DD (SEQ ID NO:12), K-CTA1R7K/C187A-Ro274-DD (SEQ ID NO:13), K-CTA1-R7K/C187A-Betv1-DD (SEQ ID NO:17), K-CTA1-R7K/C187A-Phl p1-DD (SEQ ID NO:18), and K-CTA1-R7K/C187A-Phl p5-DD (SEQ ID NO:19).
3. An immunomodulating complex being a fusion protein comprising:
(a) a mutant subunit of the ADP-ribosylating A1-subunit of the cholera toxin (CTA1) that is the CTA1-R7K/C187A mutant having the amino acid sequence of SEQ ID NO:1 or that is the K-CTA1-R7K/C187A mutant having the amino acid sequence of SEQ ID NO:2,
(b) a peptide capable of binding to a specific cellular receptor wherein said peptide is a dimer of a Protein A D-subunit; and
(c) one or more epitopes associated with an autoimmune disease, wherein,
in the mutant CTA1 subunit, the amino acids corresponding to the amino acid 7, arginine, and the amino acid 187, cysteine, in the native CTA1 have been replaced with lysine at amino acid 7 and alanine at amino acid 187.