Chimeric peptides as immunogens, antibodies thereto, and methods for immunization using chimeric peptides or antibodies
The invention provides a chimeric peptide or mixture of chimeric peptides that can be formulated as an immunizing composition and used in a method for immunization of a mammal against an internal peptide cleavage product derived from a precursor or mature protein, for which the peptide cleavage product and the precursor or mature protein are self molecules. The chimeric peptide or peptides have an end-specific B cell epitope from a naturally-occurring internal peptide cleavage product of a precursor or mature protein, as a free N- or C-terminus, fused with or without spacer residues to a T helper cell epitope derived from a living source different from that of the internal peptide cleavage product.
1. A chimeric peptide represented by formula (I) or formula (II),
N-(S) m -(T h ) n (I)
(T h ) n -(S) m -C (II)
or chimeric peptides which are mixtures of formula (I) peptides, mixtures of formula (II) peptides, or mixtures of formula (I) and formula (II) peptides, wherein:
N is the first 2, 3, 4, or 5 amino acid residues from the free N-terminus of a naturally-occurring amyloid β peptide that is formed by proteolytic cleavage of β amyloid precursor protein (βAPP);
C is the last 2, 3, 4, or 5 amino acid residues from the free C-terminus of a naturally-occurring amyloid β peptide that is formed by proteolytic cleavage of β amyloid precursor protein (βAPP);
T h is a promiscuous T helper cell epitope;
S is a spacer amino acid residue;
m is 0, 1, 2, 3, 4, or 5; and
n is 1, 2, 3, or 4.
2. The chimeric peptide or peptides according to claim 1 , wherein said amyloid β peptide is selected from the group consisting of SEQ ID NOs:2, 3, 4, 5, 6, and 7.
3. The chimeric peptide or peptides according to claim 1 , wherein N is the first 2 or 3 amino acid residues from the free N-terminus of said amyloid β peptide.
4. The chimeric peptide or peptides according to claim 1 , wherein C is the last 2 or 3 amino acid residues from the free C-terminus of said amyloid β peptide.
5. The chimeric peptide or peptides according to claim 1 , wherein said promiscuous T helper cell epitope is a T cell epitope from tetanus toxin, pertussis toxin, diphtheria toxin, measles virus F protein, hepatitis B virus surface antigen, Chlamydia trachomitis major outer membrane protein, Plasmodium falciparum circumsporozoite, Schistosoma mansoni triose phosphate isomerase, or Escherichia coli TraT.
6. The chimeric peptide or peptides according to claim 5 , wherein said promiscuous T helper cell epitope has an amino acid sequence selected from the group consisting of SEQ ID NOs: 8 to 27.
7. The chimeric peptide or peptides according to claim 1 , wherein S is glycine.
8. An immunizing composition, comprising an immunizing effective amount of the chimeric peptide or peptides according to claim 1 and a pharmaceutically acceptable carrier, excipient, diluent, or auxiliary agent.
9. The immunizing composition according to claim 8 , wherein said pharmaceutically acceptable auxiliary agent is an adjuvant.
10. The immunizing composition according to claim 9 , wherein said adjuvant is alum.
11. A method for immunization against a free N-terminus or free C-terminus of an amyloid β peptide, comprising administering to a mammal the immunizing composition according to claim 8 , for which the amyloid β peptide is a self molecule of the mammal.
12. The method according to claim 11 , wherein the mammal is a human.
13. A chimeric peptide of formula (I) or formula (II),
N-(S) m -(Th) n (I)
(Th) n -(S) m -C (II)
or chimeric peptides which are mixtures of formula (I) peptides, mixtures of formula (II) peptides, or mixtures of formula (I) and formula (II) peptides, wherein:
N is the first 2, 3, or 4 amino acid residues from the free N-terminus of a naturally-occurring internal amyloid β peptide cleavage product that is formed by proteolytic cleavage of an amyloid precursor protein;
C is the last 2, 3, or 4 amino acid residues from the free C-terminus of a naturally-occurring internal amyloid 13 peptide cleavage product, that is formed by proteolytic cleavage of an amyloid precursor protein;
T h is a promiscuous T helper cell epitope;
S is a spacer amino acid residue;
m is 0, 1, 2, 3, 4, or 5; and
n is 1, 2, 3, or 4.
14. The chimeric peptide or peptides according to claim 13 , wherein m is 1, 2, 3, 4 or 5.
15. The chimeric peptide or peptides according to claim 13 , wherein said internal amyloid β peptide cleavage product has an amino acid sequence selected from the group consisting of SEQ ID NOs: 2, 3, 4, 5, 6, and 7.
16. The chimeric peptide or peptides according to claim 13 , wherein said promiscuous T helper cell epitope is a T cell epitope from tetanus toxin, pertussis toxin, diphtheria toxin, measles virus F protein, hepatitis B virus surface antigen, Chlamydia trachomitis major outer membrane protein, Plasmodium falciparum circumsporozoite, Schistosoma mansoni triose phosphate isomerase, or Escherichia coli TraT.
17. The chimeric peptide or peptides according to claim 16 , wherein N is the first 2 or 3 amino acid residues from the free N-terminus of said internal amyloid β peptide cleavage product.
18. The chimeric peptide or peptides according to claim 16 , wherein C is the last 2 or 3 amino acid residues from the free C-terminus of said internal amyloid β peptide cleavage product.
19. The chimeric peptide or peptides according to claim 16 , wherein said promiscuous T helper cell epitope has an amino acid sequence selected from the group consisting of SEQ ID NOs: 8 to 27.
20. The chimeric peptide or peptides according to claim 13 , wherein S is glycine.
21. An immunizing composition, comprising an immunizing effective amount of the chimeric peptide or peptides according to claim 13 and a pharmaceutically acceptable carrier, excipient, diluent, or auxiliary agent.
22. The immunizing composition according to claim 21 , wherein said pharmaceutically acceptable auxiliary agent is an adjuvant.
23. The immunizing composition according to claim 22 , wherein said adjuvant is alum.
24. A method for immunization against the free N-terminus or free C-terminus of an amyloid β peptide, comprising administering to a mammal the immunizing composition according to claim 21 , for which the amyloid β peptide is a self molecule of the mammal.
25. The method according to claim 24 , wherein the mammal is a human.