IP Library Granted Patent US 10,072,061
Granted Patent B2
US 10,072,061 · App. 15/730,441 · Granted Sep 11, 2018

Tumor targeted TNF-related apoptosis inducing ligand fusion polypeptide, methods and uses therefor

Inventors: Dirk Spitzer (Webster Groves, MO); William G Hawkins (Olivette, MO)
Assignee: Washington University
C07K14/705A61K38/17C07K14/4747C07K14/70575C12N15/62C12N15/63A61K38/00A61K38/177A61K38/1761A61K38/1764A61K38/191C07K14/4748C07K14/525C07K2319/00C07K2319/21C07K2319/33C07K2319/43C07K2319/74C12N15/70C12N15/74C12N15/79
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Quick Facts
Patent No.
US 10,072,061
App. No.
15/730,441
Granted
Sep 11, 2018
Kind
B2
Abstract

Fusion polypeptides comprising a TRAIL trimer and a targeting domain are disclosed. The targeting domain can be, in some embodiments, a sequence that binds MUC16, which is prevalent on some tumor cells such as pancreatic and ovarian tumor cells. A sequence that binds MUC 16 can be mesothelin or a MUC16-binding fragment thereof, such as amino acids 1-64 of mesothelin. A fusion polypeptide of the present teachings can induce apoptosis in a target cell such as a MUC16-expressing cancer cell. Also disclosed are nucleic acids encoding the fusion polypeptides, and methods of use of the fusion polypeptides and nucleic acids.

Claims (12)

1. A method of reducing metastatic potential of tumor cells in a subject in need thereof, comprising administering to a subject in need thereof a fusion polypeptide comprising a mesothelin polypeptide and three consecutive extracellular domains of TNF-related apoptosis-inducing ligand (TRAIL) fused together in a head-to-tail configuration.

2. A method in accordance with claim 1 , wherein the mesothelin polypeptide is a full-length mesothelin polypeptide.

3. A method in accordance with claim 1 , wherein the mesothelin polypeptide is meso64.

4. A method in accordance with claim 1 , wherein the mesothelin polypeptide is mesothelinΔGPI.

5. A method of reducing metastatic potential of a tumor cell in a subject in need thereof, comprising contacting a cell expressing MUC16 with a fusion polypeptide comprising a mesothelin polypeptide and three consecutive extracellular domains of TNF-related apoptosis-inducing ligand (TRAIL) fused together in a head-to-tail configuration.

6. A method in accordance with claim 5 , wherein the mesothelin polypeptide is a full-length mesothelin polypeptide.

7. A method in accordance with claim 5 , wherein the mesothelin polypeptide is meso64.

8. A method in accordance with claim 5 , wherein the mesothelin polypeptide is mesothelinΔGPI.

9. A method of selectively killing a MUC16-positive cell within a population of cells, comprising contacting the MUC16-positive cell with an effective amount of a fusion polypeptide comprising a mesothelin polypeptide and three consecutive extracellular domains of TNF-related apoptosis-inducing ligand (TRAIL) fused together in a head-to-tail configuration.

10. A method in accordance with claim 9 , wherein the mesothelin polypeptide is a full-length mesothelin polypeptide.

11. A method in accordance with claim 9 , wherein the mesothelin polypeptide is meso64.

12. A method in accordance with claim 9 , wherein the mesothelin polypeptide is mesothelinΔGPI.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 29, 2019
From: WASHINGTON UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 048176/0697 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2017
From: SPITZER, DIRK M.; HAWKINS, WILLIAM G.
To: WASHINGTON UNIVERSITY
Reel/Frame 044036/0905 →
Continuity (4)
Continuation 14798045 · Jul 13, 2015
Continuation 13892238 · May 10, 2013
Provisional Application 61645058 · May 10, 2012
Related Publication 20180030109A1 · Feb 1, 2018