IP Library Granted Patent US 7,449,450
Granted Patent B2
US 7,449,450 · App. 11/104,506 · Granted Nov 11, 2008

Compounds, methods of screening, and in vitro and in vivo uses involving anti-apoptotic genes and anti-apoptotic gene products

Assignee: Immunogen Inc.
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Quick Facts
Patent No.
US 7,449,450
App. No.
11/104,506
Granted
Nov 11, 2008
Kind
B2
Abstract

Novel polypeptides having anti-apoptotic activity, and methods of screening for such novel polypeptides having anti-apoptotic activity, and polynucleotides encoding such polypeptides; Compounds that regulate or modulate apoptosis and/or anti-apoptotic activity, such as compounds having anti-apoptotic activity, and such as compounds that induce, restore, or modulate apoptosis and/or inhibit, diminish, or modulate anti-apoptotic activity, methods of screening for such compounds, and methods of using such compounds in the therapeutic treatment of diseases; Methods of treating eukaryotic cells with compounds that regulate or modulate apoptosis and/or anti-apoptotic activity; Methods of enhancing the stability, growth, and/or productivity of eukaryotic cells; Pharmaceutical compositions that regulate or modulate apoptosis and/or anti-apoptotic activity.

Claims (19)

1. A composition comprising a therapeutically effective amount of an agent, which is an antisense oligonucleotide which binds to a polynucleotide which encodes human cytomegalovirus pUL37s, wherein the therapeutically effective amount is an amount that restores apoptosis in CMV-infected cells.

2. The composition of claim 1 , wherein said antisense oligonucleotide comprises a phosphorothioate backbone.

3. A pharmaceutical composition comprising a pharmaceutically-acceptable carrier or excipient, and a therapeutically effective amount of an agent, which is an antisense oligonucleotide which binds to a polynucleotide which encodes human cytomegalovirus pUL37s, wherein the therapeutically effective amount is an amount that restores apoptosis in CMV-infected cells.

4. The composition of claim 1 , wherein said antisense oligonucleotide comprises at least 25 consecutive nucleotides of a polynucleotide which encodes human cytomegalovirus pUL37s.

5. The composition of claim 1 , wherein said antisense oligonucleotide comprises methylphosphonate moieties.

6. The composition of claim 1 , wherein said antisense oligonucleotide is soluble.

7. The composition of claim 1 , wherein said antisense oligonucleotide comprises at least one modified internucleoside linkage.

8. The antisense composition of claim 7 , wherein the modified internucleoside linkage is a phosphorothioate linkage.

9. The antisense composition of claim 1 wherein said antisense oligonucleotide comprises at least one modified nucleobase.

10. A method for modulating apoptosis in a cell expressing pUL37s, said method comprising: contacting said cell with a composition comprising a therapeutically effective amount of an agent, wherein said agent is an antisense oligonucleotide which binds to a polynucleotide which encodes human cytomegalovirus pUL37s, wherein the therapeutically effective amount is an amount that restores apoptosis in CMV-infected cells.

11. The method of claim 10 , wherein said antisense oligonucleotide comprises a phosphorothioate backbone.

12. A method for modulating apoptosis, said method comprising: contacting a eukaryotic cell with an effective amount of a composition according to any one of claims 1 to 9 .

13. The method of claim 10 , wherein said composition comprises a pharmaceutically-acceptable carrier or excipient.

14. The method of claim 10 , wherein said antisense oligonucleotide comprises at least 25 consecutive nucleotides of a polynucleotide which encodes human cytomegalovirus pUL37s.

15. The method of claim 10 , wherein said antisense oligonucleotide comprises methyiphosphonate moieties.

16. The method of claim 10 , wherein said antisense oligonucleotide is soluble.

17. The method of claim 10 , wherein said antisense oligonucleotide comprises at least one modified internucleoside linkage.

18. The method of claim 10 , wherein said antisense oligonucleotide comprises at least one modified internucleoside linkage, wherein said internucleoside linkage is a phosphorothioate linkage.

19. The method of claim 10 , wherein said antisense oligonucleotide comprises at least one modified nucleobase.

Assignments (2)
ADDRESS CHANGE Recorded May 13, 2008
From: IMMUNOGEN, INC.
To: IMMUNOGEN, INC.
Reel/Frame 020930/0905 →
MERGER Recorded Feb 25, 2008
From: APOPTOSIS TECHNOLOGY, INC.
To: IMMUNOGEN INC.
Reel/Frame 020554/0732 →
Continuity (5)
Continuation 1046380800 · Jun 18, 2003
Division 0971650400 · Nov 21, 2000
Continuation In Part 0930112100 · Apr 28, 1999
Continuation In Part 0908026500 · May 18, 1998
Related Publication 20050191696A1 · Sep 1, 2005