IP Library Granted Patent US 8,916,174
Granted Patent B2
US 8,916,174 · App. 13/185,164 · Granted Dec 23, 2014

HIV DNA vaccine regulated by a caev-derived promoter

Inventors: Opendra Narayan (Lenexa, KS); Yahia Chebloune (Grenoble, FR)
Assignees: National Institute for Agricultural Research; University of Kansas Medical Center
A61K39/21A61K2039/53C12N2740/16034A61K2039/55522
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Quick Facts
Patent No.
US 8,916,174
App. No.
13/185,164
Granted
Dec 23, 2014
Kind
B2
Abstract

The present invention is directed to a DNA vaccine for immunization against HIV. The invention comprises a DNA molecule that has a sequence encoding a plurality of viral proteins capable of stimulating an immune response against HIV. The DNA molecule is rendered safe for use as a vaccine by the disruption of genes encoding reverse transcriptase, integrase, and Vif. The DNA molecule is further rendered safe by at least a partial deletion of the 3′ LTR.

Claims (11)

1. A DNA composition capable of stimulating an immune response comprising: a promoter sequence derived from Caprine Arthritis Encephalitis Goat Lentivirus (CAEV) operably linked to a coding sequence, wherein the coding sequence encodes a gag gene, a pro gene, a vpx gene, a vpr gene, a vpu gene, a nef gene, a tat gene, an env gene, and a rev gene, wherein the genes are of an immunodeficiency viral genome selected from the group consisting of Human Immunodeficiency Virus (HIV), Simian Immunodeficiency Virus (SIV), and combinations thereof, wherein the coding sequence is operably linked to a polyadenylation sequence, and wherein the DNA composition does not include functional reverse transcriptase (rt), integrase (int), and viral infectivity factor (vif).

2. The DNA composition of claim 1 , wherein the coding sequence encodes at least one non-functional gene.

3. The DNA composition of claim 1 , wherein the polyadenylation sequence is an SV40 polyadenylation sequence.

4. The DNA composition of claim 1 , wherein the DNA composition is in a pharmaceutically acceptable carrier.

5. A pharmaceutical composition comprising:

(a) a DNA composition having a promoter sequence derived from Caprine Arthritis Encephalitis Goat Lentivirus (CAEV) operably linked to a coding sequence, wherein the coding sequence encodes a gag gene, a pro gene, a vpx gene, a vpr gene, a vpu gene, a nef gene, a tat gene, an env gene, and a rev gene, wherein the genes are of an immunodeficiency viral genome selected from the group consisting of Human Immunodeficiency Virus (HIV), Simian Immunodeficiency Virus (SIV), and combinations thereof, wherein the coding sequence is operably linked to a polyadenylation sequence, and wherein the DNA composition does not include functional reverse transcriptase (rt), integrase (int), and viral infectivity factor (vif); and,

(b) a pharmaceutically acceptable carrier.

6. The pharmaceutical composition of claim 5 , wherein the coding sequence encodes at least one non-functional gene.

7. The pharmaceutical composition of claim 5 , wherein the promoter sequence is a 5′ long terminal repeat (LTR) of SIV.

8. The pharmaceutical composition of claim 5 , wherein the DNA composition lacks a functional 3′ LTR sequence.

9. The pharmaceutical composition of claim 5 , wherein the polyadenylation sequence is an SV40 polyadenylation sequence.

Assignments (1)
CONFIRMATORY LICENSE Recorded Nov 30, 2017
From: UNIVERSITY OF KANSAS MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044554/0052 →
Continuity (3)
Continuation 10941164 · Sep 15, 2004
Provisional Application 60503197 · Sep 16, 2003
Related Publication 20120207782A1 · Aug 16, 2012