IP Library Granted Patent US 9,328,144
Granted Patent B2
US 9,328,144 · App. 13/892,185 · Granted May 3, 2016

HSV-1 epitopes and methods for using same

Inventors: David M. Koelle (Seattle, WA); George M. G. M. Verjans (Doetinchem, NL)
Assignees: UNIVERSITY OF WASHINGTON; Erasmus University Medical Center Rotterdam (Erasmus MC)
C07K14/005A61K39/12A61K39/245A61K2035/124A61K2039/5156A61K2039/5158A61K2039/5256A61K2039/53C07K2319/00C12N2710/10343C12N2710/16034C12N2710/16622C12N2710/16634C12N2710/24143
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,328,144
App. No.
13/892,185
Granted
May 3, 2016
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 (7)

1. A fusion protein, comprising a heterologous polypeptide fused to an immunogenic portion of HSV-1VP16 (SEQ ID NO:1), wherein said portion consists of amino acids 64-160, 90-99, 141-240, 191-203, 215-227, 218-320, 219-230, 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, or a polynucleotide encoding said fusion protein.

2. A recombinant virus comprising the polynucleotide of claim 1 .

3. The recombinant virus of claim 2 which is an adenovirus or poxvirus.

4. A pharmaceutical composition comprising the fusion protein or polynucleotide of claim 1 or the virus of claim 3 , and optionally, a pharmaceutically acceptable carrier.

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

6. A polypeptide produced by culturing a host cell transformed with a vector comprising the polynucleotide of claim 2 .

7. A method of inducing an immune response to HSV-1 in a subject comprising administering an effective amount of the composition of claim 4 to the subject.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2015
From: VERJANS, GEORGE M.G.M.
To: ERASMUS UNIVERSITY MEDICAL CENTER ROTTERDAM (ERASMUS MC)
Reel/Frame 036462/0466 →
CONFIRMATORY LICENSE Recorded Feb 11, 2015
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 034954/0821 →
CONFIRMATORY LICENSE Recorded Jan 15, 2014
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 032023/0339 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2013
From: KOELLE, DAVID M.
To: UNIVERSITY OF WASHINGTON
Reel/Frame 030503/0035 →
Continuity (3)
Division 12702218 · Feb 8, 2010
Provisional Application 61150753 · Feb 7, 2009
Related Publication 20130309262A1 · Nov 21, 2013