IP Library Granted Patent US 7,198,784
Granted Patent B2
US 7,198,784 · App. 10/661,761 · Granted Apr 3, 2007

Retroviral vectors

Assignee: Oxford Biomedica (UK) Limited
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 7,198,784
App. No.
10/661,761
Granted
Apr 3, 2007
Kind
B2
Abstract

Retroviral vector production systems for producing lentivirus-based vector particles which are capable of infecting and transducing non-dividing target cells, wherein one or more of the auxiliary genes such as vpr, vif, tat, and nef in the case of HIV-1 are absent from the system. The systems and resulting retrovirus vector particles have improved safety over existing systems and vectors.

Claims (19)

1. A lentivirus-based retroviral vector production system for producing a replication defective retroviral vector, wherein the retroviral vector production system comprises an expression construct encoding a lentivirus-based retroviral vector genome, and a separate expression construct or constructs encoding gag, pol, and an envelope protein, wherein the retroviral vector production system lacks nucleic acid sequences encoding functional tat, and wherein the retroviral vector production system is capable of producing a replication defective retroviral vector.

2. the retroviral production system according to claim 1 , wherein the nucleic acid sequences encoding tat are absent or disrupted in the vector system.

3. The retroviral vector production system according to claim 1 , further comprising a nucleic acid sequence encoding functionally active rev or RRE-type sequences.

4. The retroviral vector production system according to claim 3 , wherein at least one RRE-type sequence is a constitutive transport element (CTE).

5. The retroviral vector production system according to claim 4 , wherein the CTE is Mason Pfizer monkey virus CTE.

6. The retroviral vector production system according to claim 1 , further comprising at least one nucleotide sequence of interest (NOI).

7. The retroviral vector production system according to claim 6 , wherein the at least one NOI encodes a therapeutic protein or gene product of interest.

8. A method for producing a replication defective retroviral vector comprising at least one NOI, comprising contacting the retroviral vector production system of claim 6 with a cell, thereby producing the replication defective retroviral vector.

9. An isolated cell comprising the retroviral vector production system of claim 1 .

10. A composition comprising the retroviral vector production system of claim 1 and a carrier.

11. The retroviral vector production system according to claim 1 , wherein the system comprises separate DNA constructs which encode: (i) the lentivirus-based retroviral vector genome, (ii) gag and pol proteins, and (iii) an envelope protein.

12. The retroviral vector production system according to claim 1 , wherein the lentivirus-based retroviral vector genome comprises an operable promoter.

13. The retroviral vector production system according to claim 12 , wherein the promoter is a non-retroviral promoter.

14. The retroviral vector production system according to claim 1 , wherein the envelope protein is VSV-G.

15. The retroviral vector production system according to claim 1 , wherein the retroviral vector production system is based on HIV-1.

16. A set of separate DNA constructs comprising a DNA construct which encodes a replication-defective lentivirus-based retroviral vector genome, a DNA construct which encodes gag and pol proteins, and a DNA construct which encodes an envelope protein, wherein the set of DNA constructs lacks nucleic acid sequences encoding functional Tat.

17. The set of separate DNA constructs according to claim 16 , further comprising a DNA construct which encodes a functionally active rev or RRE-type sequences.

18. The set of separate DNA constructs according to claim 16 , wherein the DNA construct encoding the lentivirus-based retroviral vector genome further comprises at least one NOI.

19. A method for producing a replication defective retroviral vector, comprising expressing in a cell the retroviral vector production system according to claim 1 , thereby producing the replication defective retroviral vector.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Jul 11, 2017
From: OBERLAND CAPITAL SA LLC
To: OXFORD BIOMEDICA (UK) LIMITED
Reel/Frame 042975/0446 →
SECURITY INTEREST Recorded Jun 22, 2015
From: OXFORD BIOMEDICA (UK) LIMITED
To: OBERLAND CAPITAL SA LLC
Reel/Frame 035993/0501 →
CORRECTED COVER SHEET TO CORRECT 4TH ASSIGNOR'S NAME, PREVIOUSLY RECORDED AT REEL/FRAME 014785/0800 (ASSIGNMENT OF ASSIGNOR'S INTEREST) Recorded Feb 14, 2005
From: KINGSMAN, ALAN JOHN; KINGSMAN, SUSAN MARY; KIM, NARRY; MITROPHANOUS, KYRIACOS
To: OXFORD BIOMEDICA (UK) LIMITED
Reel/Frame 015708/0810 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 15, 2003
From: KINGSMAN, ALAN JOHN; KINGSMAN, SUSAN MARY; KIM, NARRY; MITRAPHANOUS, KYRIACOS
To: OXFORD BIOMEDICA (UK LIMITED)
Reel/Frame 014785/0800 →
Priority Claims (2)
GB 9621680.9 · Oct 17, 1996 · national
GB 9624457.9 · Nov 25, 1996 · national
Continuity (4)
Continuation In Part 0991516900 · Jul 25, 2001
Division 0922401400 · Dec 28, 1998
Continuation PCTGB970285700 · Oct 17, 1997
Related Publication 20040086488A1 · May 6, 2004