IP Library Granted Patent US 9,044,447
Granted Patent B2
US 9,044,447 · App. 13/262,833 · Granted Jun 2, 2015

Antigenic peptide of HSV-2 and methods for using same

Inventors: Lawrence Corey (Mercer Island, WA); Kerry J. Laing (Seattle, WA); Anna Wald (Seattle, WA); David M. Koelle (Seattle, WA)
Assignees: UNIVERSITY OF WASHINGTON; FRED HUTCHISON CANCER RESEARCH CENTER
A61K39/245A61K9/0019A61K39/00A61K2039/5158C07K14/005C12N2710/16622
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Quick Facts
Patent No.
US 9,044,447
App. No.
13/262,833
Granted
Jun 2, 2015
Kind
B2
Abstract

The invention provides HSV antigens that are useful for the prevention and treatment of HSV infection, including epitopes confirmed to be recognized by T-cells derived from herpetic lesions. 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 (21)

1. A method of enhancing proliferation of herpes simplex virus type 2 (HSV-2)-specific T cells from a subject expressing human leukocyte antigen (HLA) type B08 comprising contacting the HSV-specific T cells with a polypeptide consisting of AFEDRSYPAVFYLLQ (SEQ ID NO: 12) and up to 15 amino acids of adjacent native sequence of U L 19 (SEQ ID NO: 6), and wherein said T cells are contacted with said polypeptide in an amount sufficient to enhance proliferation of said HSV-2-specific T cells.

2. A method of inducing an immune response to herpes simplex virus type 2 (HSV-2) in a subject comprising administering a polypeptide consisting of AFEDRSYPAVFYLLQ (SEQ ID NO: 12) and up to 15 amino acids of adjacent native sequence of U L 19 (SEQ ID NO: 6) to the subject, wherein the subject is a human expressing human leukocyte antigen (HLA) type B08, and wherein the polypeptide is administered in an amount sufficient to induce an immune response in said subject.

3. A method of treating an HSV-2 infection in a subject comprising administering a therapeutically effective amount of a polypeptide consisting of AFEDRSYPAVFYLLQ (SEQ ID NO: 12) and up to 15 amino acids of adjacent native sequence of U L 19 (SEQ ID NO: 6) to the subject, wherein the subject is a human expressing human leukocyte antigen (HLA) type B08, and wherein the therapeutically effective dose of said polypeptide is administered in amount sufficient to treat an HSV-2 infection in said subject.

4. The method of claim 2 , further comprising administering an adjuvant to the subject.

5. The method of claim 1 , further comprising administering an adjuvant to the subject.

6. The method of claim 3 , further comprising administering an adjuvant to the subject.

7. The method of claim 1 , wherein the polypeptide consists of SEQ ID NO: 12 and up to 10 amino acids of adjacent native sequence of SEQ ID NO: 6.

8. The method of claim 2 , wherein the polypeptide consists of SEQ ID NO: 12 and up to 10 amino acids of adjacent native sequence of SEQ ID NO: 6.

9. The method of claim 3 , wherein the polypeptide consists of SEQ ID NO: 12 and up to 10 amino acids of adjacent native sequence of SEQ ID NO: 6.

10. The method of claim 1 , wherein the polypeptide is administered in the form of a pharmaceutically acceptable salt.

11. The method of claim 2 , wherein the polypeptide is administered in the form of a pharmaceutically acceptable salt.

12. The method of claim 3 , wherein the polypeptide is administered in the form of a pharmaceutically acceptable salt.

13. The method of claim 1 , wherein the polypeptide is co-administered with a heterologous peptide.

14. The method of claim 2 , wherein the polypeptide is co-administered with a heterologous peptide.

15. The method of claim 3 , wherein the polypeptide is co-administered with a heterologous peptide.

16. The method of claim 13 , wherein the heterologous peptide is another HSV epitope.

17. The method of claim 13 , wherein the heterologous peptide is an unrelated sequence that facilitates an immune response.

18. The method of claim 14 , wherein the heterologous peptide is another HSV epitope.

19. The method of claim 14 , wherein the heterologous peptide is an unrelated sequence that facilitates an immune response.

20. The method of claim 15 , wherein the heterologous peptide is another HSV epitope.

21. The method of claim 15 , wherein the heterologous peptide is an unrelated sequence that facilitates an immune response.

Assignments (4)
CONFIRMATORY LICENSE Recorded Oct 3, 2012
From: UNIVERSITY OF WASHINGTON / CENTER FOR COMMERCIALIZATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029067/0108 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2011
From: WALD, ANNA; KOELLE, DAVID M.
To: UNIVERSITY OF WASHINGTON
Reel/Frame 027032/0820 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2011
From: LAING, KERRY J.
To: FRED HUTCHINSON CANCER RESEARCH CENTER
Reel/Frame 027032/0855 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2011
From: COREY, LAWRENCE
To: UNIVERSITY OF WASHINGTON; FRED HUTCHINSON CANCER RESEARCH CENTER
Reel/Frame 027032/0860 →
Continuity (3)
Provisional Application 61166637 · Apr 3, 2009
Provisional Application 61228489 · Jul 24, 2009
Related Publication 20120027789A1 · Feb 2, 2012