IP Library Granted Patent US 8,460,674
Granted Patent B2
US 8,460,674 · App. 12/702,218 · Granted Jun 11, 2013

HSV-1 epitopes and methods for using same

Inventor: David M. Koelle (Seattle, WA)
Assignee: University of Washington
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Quick Facts
Patent No.
US 8,460,674
App. No.
12/702,218
Granted
Jun 11, 2013
Kind
B2
Abstract

The invention provides HSV antigens and epitopes that are useful for the prevention and treatment of HSV infection. T-cells having specificity for antigens of the invention have demonstrated cytotoxic activity against cells loaded with virally-encoded peptide epitopes, and in many cases, against cells infected with HSV. The identification of immunogenic antigens responsible for T-cell specificity provides improved anti-viral therapeutic and prophylactic strategies. Compositions containing antigens or polynucleotides encoding antigens of the invention provide effectively targeted vaccines for prevention and treatment of HSV infection.

Claims (17)

1. A pharmaceutical composition comprising an isolated HSV-1polypeptide, wherein the HSV-1polypeptide comprises an immunogenic portion of VP16, and a pharmaceutically acceptable carrier, wherein the polypeptide consists of amino acids:

64-160 , 90-99, 141-240, 187-199, 191-203, 215-227, 218-320, 219-230, 381-490, 479-489, 479-488, 480-488 or 477-490 of VP16 (SEQ ID NO: 1) and up to 50 amino acids of adjacent sequence of the original protein of SEQ ID NO: 1; optionally fused to a heterologous polypeptide, wherein the heterologous polypeptide is selected from glycoprotein L (SEQ ID NO: 2), glycoprotein K (SEQ ID NO: 3), or a fragment or combination thereof.

2. The pharmaceutical composition of claim 1 , wherein the polypeptide is a fusion protein comprising the isolated HSV polypeptide fused to glycoprotein L (SEQ ID NO: 2) or glycoprotein K (SEQ ID NO: 3).

3. The pharmaceutical composition of claim 2 , wherein the fusion protein is soluble.

4. The pharmaceutical composition of claim 1 , further comprising an adjuvant.

5. A HSV polypeptide produced by culturing a host cell transformed with a vector comprising a polynucleotide encoding an immunogenic portion of a VP16 polypeptide, wherein the polypeptide consists of amino acids 64-160, 90-99, 141-240, 187-199, 191-203, 215-227, 218-320, 219-230, 381-490, 479-489, 479-488, 480-488 or 477-490 of VP16 and up to 50 amino acids of adjacent sequence of the original protein of SEQ ID NO: 1, and recovering the polypeptide so produced.

6. A method of enhancing proliferation of HSV-specific T cells comprising contacting the HSV-specific T cells with an isolated polypeptide that comprises an immunogenic portion of VP16, wherein the polypeptide consists of amino acids 64-160, 90-99, 141-240, 187-199, 191-203, 215-227, 218-320, 219-230, 381-490, 479-489, 479-488, 480-488 or 477-490 of VP16 and up to 50 amino acids of adjacent sequence of the original protein of SEQ ID NO: 1.

7. A method of inducing an immune response to an HSV infection in a subject comprising administering the composition of claim 1 to the subject.

8. A method of treating a HSV infection in a subject comprising administering the composition of claim 1 to the subject.

9. The pharmaceutical composition of claim 1 , wherein the polypeptide is a fusion protein comprising glycoprotein L (SEQ ID NO: 2), glycoprotein K (SEQ ID NO: 3), or a fragment or combination thereof.

10. The pharmaceutical composition of claim 9 , wherein the fragment comprises amino acids 66-74 of glycoprotein L (ETDPVTFLY; SEQ ID NO: 6 or EADPVTFLY; SEQ ID NO: 8), or amino acids 201-209 of glycoprotein K (LIDGI FLRY; SEQ ID NO: 7 or RIDGIFLRY; SEQ ID NO: 9).

11. The pharmaceutical composition of claim 1 , wherein the HSV-1polypeptide consists of amino acids 90-99 or 479-488 of VP16 and up to 50 amino acids of adjacent sequence of the original protein of SEQ ID NO: 1.

12. The method of claim 7 , wherein the immune response comprises killing a HSV infected cell.

13. The method of claim 7 , wherein the immune response comprises inhibiting HSV replication.

14. The method of claim 7 , wherein the immune response comprises enhancing secretion of antiviral or immunomodulatory lymphokines.

15. The method of claim 7 , wherein the immune response comprises enhancing production of HSV-specific antibody.

16. The method of claim 7 , wherein the immune response comprises enhancing proliferation of HSV-specific T cells.

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 31, 2010
From: UNIVERSITY OF WASHINGTON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024165/0961 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2010
From: KOELLE, DAVID M.
To: UNIVERSITY OF WASHINGTON
Reel/Frame 024096/0146 →
Continuity (2)
Provisional Application 61150753 · Feb 7, 2009
Related Publication 20100203073A1 · Aug 12, 2010