IP Library Granted Patent US 8,778,352
Granted Patent B2
US 8,778,352 · App. 12/840,653 · Granted Jul 15, 2014

Polyvalent chimeric OspC vaccinogen and diagnostic antigen

Inventors: Richard Thomas Marconi (Midlothian, VA); Christopher Earnhart (Williamsburg, VA)
Assignee: Virginia Commonwealth University
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Quick Facts
Patent No.
US 8,778,352
App. No.
12/840,653
Granted
Jul 15, 2014
Kind
B2
Abstract

A chimeric polyvalent recombinant protein for use as a vaccine and diagnostic for Lyme disease is provided. The chimeric protein comprises epitopes of the loop 5 region and/or the alpha helix 5 region of outer surface protein C (OspC) types. The OspC types may be associated with mammalian Borrelia infections.

Claims (20)

1. A chimeric recombinant protein comprising

a loop 5 region of Borrelia OspC protein corresponding to amino acid residues 1-29 as set forth in SEQ ID NO: 103, and

an alpha helix 5 region of Borrelia OspC protein corresponding to amino acid residues 10-60 as set forth in SEQ ID NO: 119.

2. The chimeric recombinant protein of claim 1 , wherein said OspC types are associated with invasive Borrelia infection.

3. A method for eliciting an immune response against Borrelia in an individual in need thereof comprising the step of

administering to said individual a chimeric recombinant protein comprising

i) a loop 5 region of Borrelia outer surface protein C (OspC) protein corresponding to amino acids 1-29 as set forth in SEQ ID NO: 103; and

ii) an alpha helix 5 region of Borrelia OspC protein corresponding to amino acids 10-60 as set forth in SEQ ID NO: 119.

4. The method of claim 3 , wherein said OspC types are associated with invasive Borrelia infection.

5. A immunogenic cocktail of chimeric recombinant proteins, comprising

an ammo acid sequence comprising:

i) a loop 5 region of Borrelia outer surface protein C (OspC) protein corresponding to amino acids 1-29 as set forth in SEQ ID NO: 103; and

ii) an alpha helix 5 region of Borrelia outer surface protein C (OspC) protein corresponding to amino acids 10-60 as set forth in SEQ ID NO: 119; and

a pharmacologically suitable carrier.

6. The method of claim 3 , wherein said individual is a companion pet.

7. The chimeric recombinant protein of claim 1 , wherein antibody binding affinity exhibited by said chimeric recombinant protein is at least 50% greater than antibody binding affinity exhibited by native, intact loop 5 region or native, intact alpha helix 5 region.

8. The chimeric recombinant protein of claim 1 , wherein antibody binding affinity exhibited by said chimeric recombinant protein is at least 60% greater than antibody binding affinity exhibited by native, intact loop 5 region or native, intact alpha helix 5 region.

9. The chimeric recombinant protein of claim 1 , wherein antibody binding affinity exhibited by said chimeric recombinant protein is at least 70% greater than antibody binding affinity exhibited by native, intact loop 5 region or native, intact alpha helix 5 region.

10. The chimeric recombinant protein of claim 1 , wherein antibody binding affinity exhibited by said chimeric recombinant protein is at least 80% greater than antibody binding affinity exhibited by native, intact loop 5 region or native, intact alpha helix 5 region.

11. The chimeric recombinant protein of claim 1 , wherein antibody binding affinity exhibited by said chimeric recombinant protein is 90-100% greater than antibody binding affinity exhibited by native, intact loop 5 region or native, intact alpha helix 5 region.

Assignments (1)
CONFIRMATORY LICENSE Recorded Mar 6, 2015
From: VIRGINIA COMMONWEALTH UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 035138/0754 →
Continuity (5)
Continuation 11564433 · Nov 29, 2006
Provisional Application 60740272 · Nov 29, 2005
Provisional Application 60789588 · Apr 6, 2006
Provisional Application 60790530 · Apr 10, 2006
Related Publication 20110070257A1 · Mar 24, 2011