HSV-1 epitopes and methods for using same
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.
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.