Fusion proteins for the treatment of allergic diseases
The present invention relates to a fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a targeting unit and the second targeting unit peptide is a FGL-2 C-terminal peptide according to SEQ ID no 1. Provided herein are also uses of said fusion protein as a vaccine for treating shrimp allergy, as well as a vaccine composition and methods of its production.
1. A fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2.
2. The fusion protein according to claim 1 , wherein the allergen is shrimp tropomyosin Pan b 1 (SEQ ID No: 15) parts or fragments thereof.
3. The fusion protein according to claim 2 , wherein the fragments of shrimp tropomyosin Pan b1 comprises the sequence according to any one of SEQ ID Nos: 4, 5, 6, 7, or 8.
4. The fusion protein according to claim 1 , wherein the allergen is shrimp tropomyosin peptide 5 (P5) (SEQ ID No: 8).
5. The fusion protein according to claim 1 , wherein the allergen is shrimp tropomyosin peptide 1 (P1) (SEQ ID No: 4).
6. The fusion protein according to claim 1 , wherein said linker is RADAAP (SEQ ID No: 12).
7. The fusion protein according to claim 1 , wherein the allergen is P5 (SEQ ID No: 8) and the linker is RADAAP (SEQ ID No: 12).
8. The fusion protein according to claim 1 , wherein the allergen is P1 (SEQ ID No: 4) and the linker is RADAAP (SEQ ID No: 12).
9. A method of treating shrimp allergy comprising administering to a subject a fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2, wherein the shrimp allergy is treated.
10. A vaccine composition comprising a fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2.
11. Method for inhibiting and/or treating shrimp allergy, comprising administering to a mammal an effective amount of a fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2 or a vaccine composition comprising a fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2.
12. A kit comprising a fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2 or a vaccine composition comprising a fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a targeting unit and the second targeting unit peptide is a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2, a container comprising said fusion protein or vaccine composition and optionally instructions for its use.
13. A method for preparing a fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2, comprising the steps of:
a) providing an isolated allergen peptide from shrimp tropomyosin Pan b 1 (SEQ ID No: 15) or a fragment thereof;
b) providing a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2,
c) fusing said isolated allergen peptide and said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2 and said linker; and
d) optionally isolating said fusion protein.
14. The method according to claim 13 , wherein the fragments of shrimp tropomyosin Pan b 1 comprises the sequence according to any one of SEQ ID Nos: 4, 5, 6, 7, or 8.
15. The method according to claim 13 , wherein the linker is RADAAP (SEQ ID No: 12).
16. A method for preparing a fusion protein comprising a first peptide and a second peptide linked together with a linker, wherein the first peptide is an allergen and the second peptide is a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2, comprising the steps of:
a) providing a nucleic acid encoding an isolated allergen peptide from shrimp tropomyosin Pan b 1 (SEQ ID No: 15) or a fragment thereof;
b) providing a nucleic acid encoding a FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2,
c) fusing said nucleic acid encoding said isolated allergen peptide and said nucleic acid encoding said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1, and wherein said FGL-2 C-terminal peptide selected from the group consisting of amino acids 23-122 of SEQ ID NO:1 and sequences with at least 95% identity to amino acids 23-122 of SEQ ID NO:1 binds to human B-cells with a greater affinity than full-length FGL2 and a nucleic acid encoding said linker; and
d) optionally isolating said fusion protein.
17. The method according to claim 16 , wherein the fragments of shrimp tropomyosin Pan b 1 comprises the sequence according to any one of SEQ ID Nos: 4, 5, 6, 7, or 8.
18. The method according to claim 16 , wherein the linker is RADAAP (SEQ ID No: 12).