IP Library Granted Patent US 12,129,282
Granted Patent B2
US 12,129,282 · App. 18/316,594 · Granted Oct 29, 2024

Factor H binding protein variants and methods of use thereof

Inventor: Peter T. Beernink (Walnut Creek, CA)
Assignee: Children's Hospital & Research Center at Oakland
C07K14/22A61K39/095A61K2039/55505A61K2039/575
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Quick Facts
Patent No.
US 12,129,282
App. No.
18/316,594
Granted
Oct 29, 2024
Kind
B2
Abstract

Variant factor H binding proteins that can elicit antibodies that are bactericidal for at least one strain of Neisseria meningitidis , compositions comprising such proteins, and methods of use of such proteins, are provided.

Claims (35)

1. A variant factor H binding protein (fHbp), wherein the variant fHbp comprises:

an amino acid sequence at least 85% identical to the entire length of the amino acid sequence of fHbp ID 22 set forth in SEQ ID NO: 2; and

amino acid substitutions of lysine at position 219 with asparagine (K219N), leucine at position 130 with arginine (L130R), and glycine at position 133 with aspartic acid (G133D), each relative to the amino acid sequence set forth in SEQ ID NO:2, wherein the numbering of K219 is based on the numbering of amino acid residues in SEQ ID NO: 1.

2. The variant fHbp of claim 1 , wherein the variant fHbp differs from the sequence of SEQ ID NO: 2 by 4, 5, 6, 7, 8, 9, or 10 amino acids.

3. The variant fHbp of claim 1 , wherein the amino acid sequence of the variant fHbp is at least 95% identical to the entire length of the amino acid sequence set forth in SEQ ID NO:2.

4. The variant fHbp of claim 1 , wherein the amino acid sequence of the variant fHbp is at least 98% identical to the entire length of the amino acid sequence set forth in SEQ ID NO:2.

5. An immunogenic composition comprising:

a) the variant fHbp according to claim 1 ; and

b) a pharmaceutically acceptable excipient.

6. The immunogenic composition of claim 5 , wherein the variant fHbp is in a vesicle preparation prepared from a Neisseria meningitidis strain.

7. The immunogenic composition of claim 5 , wherein the pharmaceutically acceptable excipient comprises an adjuvant.

8. The immunogenic composition of claim 7 , wherein the adjuvant is aluminum phosphate.

9. The immunogenic composition of claim 7 , wherein the adjuvant is aluminum hydroxide.

10. The immunogenic composition of claim 6 , wherein the pharmaceutically acceptable excipient comprises an adjuvant.

11. The immunogenic composition of claim 10 , wherein the adjuvant is aluminum phosphate.

12. The immunogenic composition of claim 10 , wherein the adjuvant is aluminum hydroxide.

13. The immunogenic composition of claim 3 , further comprising Neisserial surface protein A.

14. A method of eliciting an antibody response to Neisseria meningitidis in a mammal, the method comprising administering to the mammal an immunologically effective amount of the immunogenic composition of claim 5 .

15. The method of claim 14 , wherein the mammal is a human.

16. A method of eliciting an antibody response to Neisseria meningitidis in a mammal, the method comprising administering to the mammal an immunologically effective amount of the immunogenic composition of claim 6 .

17. The method of claim 16 , wherein the mammal is a human.

18. The immunogenic composition of claim 5 , wherein said composition further comprises a second variant of factor H binding protein (fHbp), wherein the second variant comprises:

a substitution of the serine at position 223 (S223) with arginine (S223R),

wherein the numbering of the position S223 is based on the numbering of amino acid residues in SEQ ID NO:1 and wherein the second variant comprises an amino acid sequence having at least 85% amino acid sequence identity to SEQ ID NO:1.

19. The immunogenic composition of claim 18 , wherein the second variant comprises an amino acid sequence having at least 90% amino acid sequence identity to SEQ ID NO:1.

20. The immunogenic composition of claim 18 , wherein the second variant comprises an amino acid sequence having at least 95% amino acid sequence identity to SEQ ID NO:1.

21. The immunogenic composition of claim 18 , wherein the second variant fHbp differs from the sequence of SEQ ID NO: 1 by 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids.

22. The immunogenic composition of claim 18 , wherein the second variant fHbp is in a vesicle preparation prepared from a Neisseria meningitidis strain.

23. The immunogenic composition of claim 5 , wherein said composition further comprises a second variant of factor H binding protein (fHbp), wherein the second variant comprises:

a substitution of the serine at position 223 (S223) with arginine (S223R),

wherein the numbering of the position S223 is based on the numbering of amino acid residues in SEQ ID NO:1 and wherein the second variant comprises an amino acid sequence having at least 85% amino acid sequence identity to SEQ ID NO:3.

24. The immunogenic composition of claim 23 , wherein the second variant comprises an amino acid sequence having at least 90% amino acid sequence identity to SEQ ID NO:3.

25. The immunogenic composition of claim 23 , wherein the second variant comprises an amino acid sequence having at least 95% amino acid sequence identity to SEQ ID NO:3.

26. The immunogenic composition of claim 23 , wherein the second variant fHbp differs from the sequence of SEQ ID NO: 3 by 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids.

27. The immunogenic composition of claim 23 , wherein the variant fHbp is in a vesicle preparation prepared from a Neisseria meningitidis strain.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2025
From: CHILDREN'S HOSPITAL & RESEARCH CENTER AT OAKLAND
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 070003/0112 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2023
From: BEERNINK, PETER T.
To: CHILDREN'S HOSPITAL & RESEARCH CENTER AT OAKLAND
Reel/Frame 065188/0173 →
Continuity (6)
Continuation 17221646 · Apr 2, 2021
Continuation 16600282 · Oct 11, 2019
Continuation 16288760 · Feb 28, 2019
Division 15327346
Provisional Application 62028123 · Jul 23, 2014
Related Publication 20240025951A1 · Jan 25, 2024