IP Library Granted Patent US 8,227,403
Granted Patent B2
US 8,227,403 · App. 10/583,503 · Granted Jul 24, 2012

A-β immunogenic peptide carrier conjugates and methods of producing same

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Quick Facts
Patent No.
US 8,227,403
App. No.
10/583,503
Granted
Jul 24, 2012
Kind
B2
Abstract

The present invention is directed to methods of producing conjugates of Aβ peptide immunogens with protein/polypeptide carrier molecules, which are useful as immunogens, wherein peptide immunogens are conjugated to protein carriers via activated functional groups on amino acid residues of the carrier or of the optionally attached linker molecule, and wherein any unconjugated reactive functional groups on amino acid residues are inactivated via capping, thus retaining the immunological functionality of the carrier molecule, but reducing the propensity for undesirable reactions that could render the conjugate less safe or effective. Furthermore, the invention also relates to such immunogenic products and immunogenic compositions containing such immunogenic products made by such methods.

Claims (44)

1. An immunogenic conjugate having the formula:

wherein,

C is a CRM 197 carrier protein,

X d is a derivatized functional group of an amino acid residue of the carrier protein,

P is a peptide immunogen comprising an Aβ fragment covalently attached to the derivatized functional group of the amino acid residue of the carrier protein,

R is a capping molecule covalently attached to the derivatized functional group of an amino acid residue of the carrier protein, whereby the functionality of the carrier protein is preserved such that it retains its ability to elicit the desired immune responses against the peptide immunogen that would otherwise not occur without a carrier,

n is an integer greater than 0, but less than or equal to 38, and

p is an integer greater than 0, but less than 38.

2. The conjugate of claim 1 , wherein the Aβ fragment is selected from the group consisting of residues 1-3, 1-4, 1-5, 1-6, 1-7, 1-9, 1-10, 1-11, 1-12, 1-16, 1-28, 3-6, 3-7, 13-28, 15-24, 16-22, 16-23, 17-23, 17-24, 18-24, 18-25, 17-28, 25-35, 33-42, 35-40, and 35-42 of Aβ (SEQ ID NO:21).

3. The conjugate of claim 2 , wherein the Aβ fragment is residues 1-7 of Aβ (SEQ ID NO:21).

4. An immunogenic composition, comprising an immunogenic conjugate of claim 1 , together with one or more pharmaceutically acceptable excipients, diluents, and/or adjuvants.

5. The immunogenic composition of claim 4 , wherein the Aβ fragment is selected from the group consisting of residues 1-3, 1-4, 1-5, 1-6, 1-7, 1-9, 1-10, 1-11, 1-12, 1-16, 1-28, 3-6, 3-7, 13-28, 15-24, 16-22, 16-23, 17-23, 17-24, 18-24, 18-25, 17-28, 25-35, 33-42, 35-40, and 35-42 of Aβ (SEQ ID NO:21).

6. The immunogenic composition of claim 5 , wherein the Aβ fragment is residues 1-7 of Aβ (SEQ ID NO:21).

7. The immunogenic composition of claim 4 , wherein one or more adjuvants are selected from the group consisting of GM-CSF, 529 SE, IL-12, aluminum phosphate, aluminum hydroxide, Mycobacterium tuberculosis, Bordetella pertussis , bacterial lipopolysaccharides, aminoalkyl glucosamine phosphate compounds, MPL™ (3-O-deacylated monophosphoryl lipid A), a polypeptide, Quil A, STIMULON™ QS-21, a pertussis toxin (PT), an E. coli heat-labile toxin (LT), IL-1α, IL-1β, IL-2, IL-4, IL-5, IL-6, IL-7, IL-8, IL-10, IL-13, IL-14, IL-15, IL-16, IL-17, IL-18, interferon-α, interferon-β, interferon-γ, G-CSF, TNF-α and TNF-β.

8. The immunogenic conjugate of claim 1 , wherein the peptide immunogen further comprises a terminal cysteine residue and the peptide immunogen is covalently attached to the derivatized functional group of the amino acid residue of the carrier protein via the terminal cysteine residue.

9. The immunogenic conjugate of claim 8 , wherein the terminal cysteine residue is located at the carboxy-terminus of the Aβ fragment.

10. The immunogenic conjugate of claim 8 , wherein the terminal cysteine residue is located at the amino-terminus of the Aβ fragment.

11. The immunogenic conjugate of claim 9 , wherein the Aβ fragment is residues 1-7 of Aβ (SEQ ID NO:21).

12. The immunogenic conjugate of claim 1 , wherein the capping molecule is selected from the group consisting of an amino group, a hydroxyl group, a cysteamino group, an N-acetylcysteamino group, and an ethanolamino group.

13. The immunogenic conjugate of claim 12 , wherein the capping molecule is an N-acetylcysteamino group.

14. The immunogenic conjugate of claim 1 , wherein n is an integer greater than or equal to 5, but less than or equal to 25.

15. The immunogenic conjugate of claim 14 , wherein n is an integer greater than or equal to 12, but less than or equal to 20.

16. The immunogenic conjugate of claim 11 , wherein n is an integer greater than or equal to 12, but less than or equal to 15.

17. The immunogenic conjugate of claim 16 , wherein the capping molecule is an N-acetylcysteamino group.

18. An immunogenic conjugate having the formula:

wherein,

C is CRM 197 ,

X d is a derivatized lysine residue of CRM 197 ,

P is a peptide immunogen comprising residues 1-7 of Aβ (SEQ ID NO:21) and a C-terminal cysteine residue, wherein the peptide immunogen is covalently attached to the derivatized lysine residue via the C-terminal cysteine residue,

R is a capping molecule comprising N-acetylcysteamino covalently attached to the derivatized lysine residue of CRM 197 , whereby the functionality of the carrier protein is preserved such that it retains its ability to elicit a desired immune response against the peptide immunogen that would otherwise not occur without a carrier,

n is an integer greater than 0, but less than or equal to 38, and

p is an integer greater than 0, but less than or equal to 38.

19. The immunogenic conjugate of claim 18 , wherein n is an integer greater than or equal to 5, but less than or equal to 25.

20. The immunogenic conjugate of claim 19 , wherein n is an integer greater than or equal to 12, but less than or equal to 15.

21. The immunogenic conjugate of claim 20 , wherein n is 12.

22. The immunogenic conjugate of claim 20 , wherein n is 14.

23. The immunogenic conjugate of claim 20 , wherein the peptide immunogen is DAEFRHD-C (SEQ ID NO:2).

24. The immunogenic conjugate of claim 18 having the formula:

wherein,

n is an integer greater than 0, but less than or equal to 38, and

p is an integer greater than 0, but less than or equal to 38.

25. The immunogenic conjugate of claim 24 , wherein n is 12, 14 or 15.

26. The immunogenic conjugate of claim 25 , wherein n plus p equals from 20 to 22.

27. The immunogenic conjugate of claim 24 , wherein n plus p equals from 20 to 22.

Assignments (8)
CHANGE OF NAME Recorded May 5, 2015
From: JANSSEN ALZHEIMER IMMUNOTHERAPY
To: JANSSEN SCIENCES IRELAND UC
Reel/Frame 035588/0768 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2012
From: HAGEN, MICHAEL
To: WYETH LLC
Reel/Frame 028160/0683 →
CHANGE OF NAME Recorded Mar 30, 2010
From: WYETH
To: WYETH LLC
Reel/Frame 024160/0365 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2009
From: ELAN PHARMA INTERNATIONAL LIMITED
To: CRIMAGUA LIMITED; WYETH
Reel/Frame 023435/0029 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2009
From: CRIMAGUA LIMITED
To: JANSSEN ALZHEIMER IMMUNOTHERAPY; WYETH
Reel/Frame 023435/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 19, 2009
From: NEURALAB LIMITED
To: ELAN PHARMA INTERNATIONAL LIMITED
Reel/Frame 022701/0714 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2009
From: ELAN PHARMACEUTICALS, INC.
To: NEURALAB LIMITED
Reel/Frame 022698/0698 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2007
From: ARUMUGHAM, RASAPPA G.; PRASAD, A. KRISHNA
To: WYETH; ELAN PHARMACEUTICALS, INC.
Reel/Frame 019315/0037 →