IP Library Granted Patent US 10,980,874
Granted Patent B2
US 10,980,874 · App. 16/995,926 · Granted Apr 20, 2021

Recombinant herpes simplex virus 2 (HSV-2) vaccine vectors

Inventors: William Jacobs, Jr. (Pelham, NY); Pablo A. Gonzalez-Munoz (Santiago-Chile, CL); Betsy Herold (Rowayton, CT); Christopher Petro (Pleasanton, CA)
Assignee: ALBERT EINSTEIN COLLEGE OF MEDICINE
A61K39/245A61K39/12C07K14/005C12N7/00A61K2039/525A61K2039/5254A61K2039/5256A61K2039/54A61K2039/572C12N2710/16621C12N2710/16622C12N2710/16634C12N2710/16643C12N2710/16662C12N2710/16671
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Quick Facts
Patent No.
US 10,980,874
App. No.
16/995,926
Granted
Apr 20, 2021
Kind
B2
Abstract

Recombinant herpes simplex virus 2 (HSV-2) vaccine vectors, virions thereof, compositions and vaccines comprising such, and methods of use thereof are each provided.

Claims (17)

1. A method of inhibiting an HSV-2 infection in a subject or preventing a disease caused by an HSV-2 infection in a subject comprising administering to the subject a genetically engineered HSV-2 in an amount effective to prevent inhibit the HSV-2 infection or prevent the disease caused by the HSV-2 infection,

wherein the genetically engineered HSV-2 comprises a deletion of the HSV-2 glycoprotein D-encoding gene in the genome thereof and comprises a herpes simplex virus-1 (HSV-1) glycoprotein D on a lipid bilayer thereof.

2. The method of claim 1 , wherein the HSV-1 glycoprotein D is present on the lipid bilayer of the genetically engineered HSV-2 by way of infecting a cell with a HSV-2 having a deletion of an HSV-2 glycoprotein D-encoding gene, wherein the cell is or has been transfected to express the HSV-1 glycoprotein Don a cell membrane, and wherein the genetically engineered HSV-2 comprising the HSV-1 glycoprotein D on the lipid bilayer is produced from the cell.

3. The method of claim 1 , wherein the subject is administered a first dose of the genetically engineered HSV-2 subcutaneously as a priming dose and a second dose of the genetically engineered HSV-2 subcutaneously or intravaginally.

4. The method of claim 1 , wherein the disease caused by the HSV-2 infection comprises a genital ulcer, a skin vesicle, a skin ulcer, or a combination thereof.

5. A method of inhibiting or treating an HSV-1 infection in a subject or preventing or treating a disease caused by an HSV-1 infection in a subject comprising administering to the subject a genetically engineered HSV-2 in an amount effective to inhibit or treat the HSV-1 infection or prevent or treat the disease caused by the HSV-1 infection,

wherein the genetically engineered HSV-2 comprises a deletion of the HSV-2 glycoprotein D-encoding gene in the genome thereof and comprises a herpes simplex virus-1 (HSV-1) glycoprotein D on a lipid bilayer thereof.

6. The method of claim 5 , wherein the HSV-1 glycoprotein D is present on the lipid bilayer of the genetically engineered HSV-2 by way of infecting a cell with a HSV-2 having a deletion of an HSV-2 glycoprotein D-encoding gene, wherein the cell is or has been transfected to express the HSV-1 glycoprotein Don a cell membrane, and wherein the genetically engineered HSV-2 comprising the surface glycoprotein on the lipid bilayer is produced from the cell.

7. The method of claim 5 , wherein the subject is administered a first dose of the genetically engineered HSV-2 subcutaneously as a priming dose and a second dose of the genetically engineered HSV-2 subcutaneously or intravaginally.

8. The method of claim 5 , wherein the disease caused by the HSV-2 infection comprises a genital ulcer, a skin vesicle, a skin ulcer, or a combination thereof.

9. A method of inhibiting or treating an HSV-2 and HSV-1 coinfection in a subject or preventing or treating a disease caused by an HSV-2 and HSV-1 coinfection in a subject comprising administering to the subject a genetically engineered HSV-2 in an amount effective to inhibit or treat the HSV-2 and HSV-1 co-infection or prevent or treat the disease caused by the HSV-2 and HSV-1 co-infection,

wherein the genetically engineered HSV-2 comprises a deletion of the HSV-2 glycoprotein D-encoding gene in the genome thereof and comprises a herpes simplex virus-1 (HSV-1) glycoprotein D on a lipid bilayer thereof.

10. The method of claim 9 , wherein the HSV-1 glycoprotein D is present on the lipid bilayer of the genetically engineered HSV-2 by way of infecting a cell with a HSV-2 having a deletion of an HSV-2 glycoprotein D-encoding gene, wherein the cell is or has been transfected to express the HSV-1 glycoprotein Don a cell membrane, and wherein the genetically engineered HSV-2 comprising the HSV-1 glycoprotein D on the lipid bilayer is produced from the cell.

11. The method of claim 9 , wherein the subject is administered a first dose of the genetically engineered HSV-2 subcutaneously as a priming dose and a second dose of the genetically engineered HSV-2 subcutaneously or intravaginally.

12. The method of claim 9 , wherein the disease caused by the HSV-2 infection comprises a genital ulcer, a skin vesicle, a skin ulcer, or a combination thereof.

13. A method of preventing an HSV-1 or HSV-2 latent infection in a subject comprising administering to the subject a genetically engineered HSV-2 in an amount effective to prevent the HSV-1 or HSV-2 latent infection,

wherein the genetically engineered HSV-2 comprises a deletion of the HSV-2 glycoprotein D-encoding gene in the genome thereof and comprises a herpes simplex virus-1 (HSV-1) glycoprotein D on a lipid bilayer thereof.