IP Library Granted Patent US 8,512,709
Granted Patent B2
US 8,512,709 · App. 13/124,260 · Granted Aug 20, 2013

Modified amyloid β peptide

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Quick Facts
Patent No.
US 8,512,709
App. No.
13/124,260
Granted
Aug 20, 2013
Kind
B2
Abstract

An object of the invention is to provide a peptide based on a sequence of an amyloid β peptide that may allow for induction of enhanced immune response and is safe and efficacious for prophylaxis and treatment of Alzheimer disease. An amyloid β peptide or a portion thereof with addition or insertion of cysteine or a cysteine analogue, and a method for enhancing immune response to amyloid β using said peptide, a medicament for prophylaxis and treatment of Alzheimer disease using said amyloid β peptide that induces an enhanced immune response, and a DNA vaccine comprising a gene coding for an amyloid β peptide or a sequence derived from an amyloid β peptide with addition or insertion of cysteine or a cysteine analogue, as expected to be similarly efficacious.

Claims (23)

1. A peptide consisting of peptide (a) and peptide (b), wherein:

peptide (a) is selected from the group consisting of a peptide of the amino acid residues No. 1 to No. 10 from the N-terminal of SEQ ID NO:1, a peptide of the amino acid residues No. 2 to No. 10 from the N-terminal of SEQ ID NO:1, a peptide of the amino acid residues No. 3 to No. 10 from the N-terminal of SEQ ID NO:1, a peptide of the amino acid residues No. 1 to No. 9 from the N-terminal of SEQ ID NO:1, a peptide of the amino acid residues No. 2 to No. 9 from the N-terminal of SEQ ID NO:1, and a peptide of the amino acid residues No. 1 to No. 18 from the N-terminal of SEQ ID NO:1, and

peptide (b) is selected from the group consisting of a peptide of the amino acid residues No. 28 to No. 36 from the N-terminal of SEQ ID NO:1, a peptide of the amino acid residues No. 28 to No. 37 from the N-terminal of SEQ ID NO:1, a peptide of the amino acid residues No. 28 to No. 38 from the N-terminal of SEQ ID NO:1, a peptide of the amino acid residues No. 28 to No. 39 from the N-terminal of SEQ ID NO:1, a peptide of the amino acid residues No. 28 to No. 40 from the N-terminal of SEQ ID NO:1, a peptide of the amino acid residues No. 28 to No. 41 from the N-terminal of SEQ ID NO:1, and a peptide of the amino acid residues No. 28 to No. 42 from the N-terminal of SEQ ID NO:1,

wherein the C-terminal of peptide (a) is bound to the N-terminal of peptide (b), and wherein cysteine or a cysteine analog is bound to the C-terminal of a resulting combination of peptide (a) and peptide (b).

2. The peptide of claim 1 , wherein a cysteine analog is bound to the C-terminal of the resulting combination of peptide (a) and peptide (b), and the cysteine analog is homocysteine.

3. The peptide of claim 1 , wherein the peptide

has a sequence of any one of SEQ ID NO:2 to SEQ ID NO:13.

4. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:2.

5. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:3.

6. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:4.

7. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:5.

8. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:6.

9. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:7.

10. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:8.

11. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:9.

12. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:10.

13. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:11.

14. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:12.

15. The peptide of claim 1 , wherein the peptide has a sequence of SEQ ID NO:13.

16. A medicament, comprising, as an active ingredient, the peptide of claim 1 ,

wherein the medicament is suitable for treatment of Alzheimer disease.

17. A method for inducing an immune response to amyloidβ, comprising administering to a subject in need thereof, an effective amount of the peptide of claim 1 .

18. A method for making a medicine, comprising combining the peptide of claim 1 with a pharmaceutically acceptable carrier.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2020
From: THE CHEMO-SERO-THERAPEUTIC RESEARCH INSTITUTE
To: KM BIOLOGICS CO., LTD.
Reel/Frame 051520/0971 →
CHANGE OF ADDRESS OF ASSIGNEE Recorded Apr 15, 2019
From: THE CHEMO-SERO-THERAPEUTIC RESEARCH INSTITUTE
To: THE CHEMO-SERO-THERAPEUTIC RESEARCH INSTITUTE
Reel/Frame 050169/0778 →
CORPORATE ADDRESS CHANGE Recorded Jan 16, 2013
From: THE CHEMO-SERO-THERAPEUTIC RESEARCH INSTITUTE
To: THE CHEMO-SERO THERAPEUTIC RESEARCH INSTITUTE
Reel/Frame 029637/0102 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2011
From: MATSUDA, JUNICHI; KAMINAKA, KAZUYOSHI; NOZAKI, CHIKATERU
To: THE CHEMO-SERO-THERAPEUTIC RESEARCH INSTITUTE
Reel/Frame 026160/0930 →