IP Library Granted Patent US 9,757,444
Granted Patent B2
US 9,757,444 · App. 14/820,452 · Granted Sep 12, 2017

Immunogenic compositions for the prevention and treatment of meningococcal disease

Inventors: Gary W. Zlotnick (New Windsor, NY); Leah Diane Fletcher (Geneseo, NY); John Erwin Farley (Chapel Hill, NC); Liesel A. Bernfield (Rochester, NY); Robert J. Zagursky (Victor, NY); Benjamin J. Metcalf (Rochester, NY)
Assignee: Wyeth Holdings LLC
A61K39/095A61K39/39A61K47/4833C07K14/22C07K16/1217C12N9/2417C12N9/2465C12N9/2471G01N33/56911A61K39/00A61K2039/505A61K2039/53A61K2039/54A61K2039/55505A61K2039/55572A61K2039/55577A61K2039/58A61K2039/6087G01N2333/22Y10S530/825
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,757,444
App. No.
14/820,452
Granted
Sep 12, 2017
Kind
B2
Abstract

The present invention relates to Neisseria ORF2086 proteins, crossreactive immunogenic proteins which can be isolated from nesserial strains or prepared recombinantly, including immunogenic portions thereof, biological equivalents thereof, antibodies that immunospecifically bind to the foregoing and nucleic acid sequences encoding each of the foregoing, as well as the use of same in immunogenic compositions that are effective against infection by Neisseria meningitidis serogroup B.

Claims (11)

1. A method of inducing a bactericidal immune response against serogroup B Neisseria meningitidis in a mammal comprising administering to said mammal a composition comprising an immunologically effective amount of a purified rP2086 polypeptide of strain 8529 of Neisseria meningitidis , wherein the polypeptide consists of the amino acid sequence of the full-length LP2086 polypeptide of the 8529 strain lacking its leader peptide and having methionine in place of its N-terminal cysteine amino acid residue site of fatty acid acylation, wherein the immunologically effective amount is at least 10 micrograms.

2. The method of claim 1 , wherein the polypeptide is expressed as a fusion protein.

3. The method of claim 2 , wherein the fusion protein is the non-lipidated rP2086T7 fusion protein, wherein the T7 tag sequence is fused to the amino terminus of the full length 2086 amino acid sequence of the strain 8529 lacking its leader peptide and having methionine in place of its N-terminal cysteine amino acid residue site of fatty acid acylation.

4. The method of claim 1 , wherein the immunologically effective amount is 25 micrograms.

5. The method of claim 1 , wherein the polypeptide is adjuvanted with QS-21.

6. The method of claim 1 , wherein the composition further comprises a pharmaceutically acceptable buffer, diluent, carrier, or adjuvant.

7. The method of claim 6 , wherein the adjuvant is aluminum hydroxide or aluminum phosphate.

8. The method of claim 1 , wherein the composition elicits a bactericidal immune response against a strain of serogroup B Neisseria meningitidis that is heterologous to the 8529 strain of Neisseria meningitidis.

9. The method of claim 1 , wherein the polypeptide consists of the amino acid sequence of SEQ ID NO: 216.

10. The method of claim 1 , wherein the mammal is a human.

11. A method of inducing a bactericidal immune response against a serogroup B Neisseria meningitidis in a mammal comprising administering to said mammal a composition comprising an immunologically effective amount of a purified polypeptide consisting of the amino acid sequence of SEQ ID NO: 216, wherein the immunologically effective amount is at least 10 micrograms.

Continuity (6)
Division 13455268 · Apr 25, 2012
Continuation 13333123 · Dec 21, 2011
Division 10492427
Provisional Application 60406934 · Aug 30, 2002
Provisional Application 60328101 · Oct 11, 2001
Related Publication 20150335724A1 · Nov 26, 2015