IP Library Granted Patent US 11,266,732
Granted Patent B2
US 11,266,732 · App. 15/965,246 · Granted Mar 8, 2022

Recombinant HCMV and RHCMV vectors and uses thereof

Inventors: Louis Picker (Portland, OR); Jay A. Nelson (Lake Oswego, OR); Klaus Frueh (Portland, OR); Michael A. Jarvis (Portland, OR); Scott G. Hansen (Portland, OR)
Assignee: Oregon Health & Science University
A61K39/12A61K39/0011A61K39/08A61K39/13A61K39/145A61K39/21A61K39/275C12N7/00C12N15/86C12N15/869A61K2039/5254A61K2039/5256A61K2039/552A61K2039/572A61K2039/58C07K14/005C07K14/045C07K14/16C07K14/161C07K14/162C07K14/163C12N2710/16111C12N2710/16134C12N2710/16141C12N2710/16143C12N2710/16162C12N2710/16171C12N2710/24134C12N2730/10134C12N2740/15022C12N2740/15034C12N2740/16034C12N2760/14134C12N2760/16134C12N2770/32634Y02A50/30
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 11,266,732
App. No.
15/965,246
Granted
Mar 8, 2022
Kind
B2
Abstract

The present disclosure relates to recombinant rhesus cytomegalovirus (RhCMV) and human cytomegalovirus (HCMV) vectors encoding heterologous antigens, such as pathogen-specific antigens or tumor antigens, which may be used, for example, for the treatment or prevention of infectious disease or cancer. The recombinant RhCMV or HCMV vectors elicit and maintain high level cellular immune responses specific for the heterologous antigen while including deletions in one or more genes essential or augmenting for CMV replication, dissemination or spread.

Claims (13)

1. A recombinant viral vector comprising a nucleic acid sequence encoding a human cytomegalovirus (HCMV) backbone vector and at least one heterologous antigen, wherein:

(a) the at least one heterologous antigen is a pathogen-specific antigen or a tumor antigen;

(b) the recombinant viral vector comprises a deletion in the HCMV UL115 gene that eliminates expression of a functional gL protein; and

(c) the recombinant viral vector comprises a deletion in the UL128 gene, a deletion in the UL130 gene, a deletion in the UL146 gene, and a deletion in the UL147 gene.

2. The recombinant viral vector of claim 1 , further comprising a deletion in a HCMV gene region selected from the group consisting of: the RL11 family, the pp65 family, the US12 family, and the US28 family.

3. The recombinant viral vector of claim 1 , further comprising a deletion in UL64 or US29, or a combination thereof.

4. The recombinant viral vector of claim 1 , further comprising a deletion in at least one immune modulatory HCMV gene selected from the group consisting of: US2, US3, US4, US5, US6, US7, US8, US9, US10, US11, UL118, UL119, UL36, UL37, and UL111a.

5. The recombinant viral vector of claim 1 , wherein UL122 and/or UL79 are inactivated or deleted.

6. The recombinant viral vector of claim 1 , wherein the heterologous antigen is a herpes simplex virus (HSV)-1 antigen, a HSV-2 antigen, a human papilloma virus (HPV) antigen, a hepatitis B virus antigen, or a prostate cancer antigen.

7. The recombinant viral vector of claim 1 , wherein the heterologous antigen is a Mycobacterium tuberculosis antigen.

8. The recombinant viral vector of claim 1 , wherein the heterologous antigen is Gag, Pol, Env, Rev, Tat, or Nef, or an epitope or antigenic fragment or combination thereof.

9. A method of treating a subject with an infectious disease or cancer comprising administering to the subject in need thereof a recombinant viral vector according to claim 1 .

10. A method of inducing a tumor-specific or pathogen-specific immune response in a subject at risk of developing cancer or becoming infected with an infectious disease comprising administering to the subject in need thereof a recombinant viral vector according to claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2021
From: PICKER, LOUIS; NELSON, JAY A.; FRUEH, KLAUS; JARVIS, MICHAEL A.; HANSEN, SCOTT G.
To: OREGON HEALTH & SCIENCE UNIVERSITY
Reel/Frame 058506/0839 →
Continuity (7)
Continuation 14872756 · Oct 1, 2015
Division 13694280 · Nov 14, 2012
Continuation In Part PCTUS2011036657 · May 16, 2011
Continuation In Part PCTUS2011029930 · Mar 25, 2011
Provisional Application 61376911 · Aug 25, 2010
Provisional Application 61334976 · May 14, 2010
Related Publication 20190099479A1 · Apr 4, 2019