IP Library Granted Patent US 11,834,476
Granted Patent B2
US 11,834,476 · App. 17/065,386 · Granted Dec 5, 2023

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 11,834,476
App. No.
17/065,386
Granted
Dec 5, 2023
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 (22)

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

an amino acid substitution of glycine at position with serine 220 (G220S), relative to the amino acid sequence set forth in SEQ ID NO:2, wherein the numbering of G220 is based on the numbering of amino acid residues in SEQ ID NO:1.

2. The variant fHbp of claim 1 , comprising the amino acid substitutions G220S, L130R and G133D.

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

4. 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.

5. 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.

6. An immunogenic composition comprising:

a) the variant fHbp according to claim 1 ; and

b) a pharmaceutically acceptable excipient.

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

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

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

10. The immunogenic composition of claim 8 , wherein the adjuvant is aluminum hydroxide.

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

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

13. The immunogenic composition of claim 11 , wherein the adjuvant is aluminum hydroxide.

14. The immunogenic composition of claim 6 , further comprising Neisserial surface protein A.

15. 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 .

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

17. 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 7 .

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

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 Jan 8, 2021
From: BEERNINK, PETER T.
To: CHILDREN'S HOSPITAL & RESEARCH CENTER AT OAKLAND
Reel/Frame 054856/0681 →
Continuity (5)
Continuation 16600259 · Oct 11, 2019
Continuation 16288760 · Feb 28, 2019
Division 15327346
Provisional Application 62028123 · Jul 23, 2014
Related Publication 20210101942A1 · Apr 8, 2021
Cited By (1)
US 12,269,849