IP Library › Granted Patent US 9,050,269
Granted Patent B2
US 9,050,269 · App. 12/721,287 · Granted Jun 9, 2015

Protection of virus particles from phagocytosis by expression of CD47

Inventors: Dennis E. Discher (Philadelphia, PA); Richard Kuo-An Tsai (Boston, MA)
Assignee: The Trustees of the University of Pennsylvania
A61K9/5184C07K14/705A61K35/13A61K39/12A61K47/48776A61K48/00A61K2039/5256C12N7/00C12N2740/15051
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Quick Facts
Patent No.
US 9,050,269
App. No.
12/721,287
Granted
Jun 9, 2015
Kind
B2
Abstract

The present invention relates to a viral particle. The viral particle has a radius of less than about 1 μm, and at least one peptide comprising at least a biologically active portion of CD47. The present invention also includes a method of increasing the life of a particle in vivo in a mammal. The method includes the steps of expressing at least one peptide comprising at least a biologically active portion of CD47 in a viral particle, and administering the viral particle having CD47 expressed to a mammal, wherein the administered viral particle has a longer half life in the mammal than an otherwise identical viral particle that does not have CD47 expressed thereon.

Claims (23)

1. A composition comprising:

a viral particle having a radius of less than about 400 nm; and,

at least one peptide comprising SEQ ID NO:2,

wherein said at least one peptide is expressed on an exposed surface of said viral particle.

2. The composition of claim 1 , wherein said particle has a radius of less than about 150 nm.

3. The composition of claim 1 , wherein said particle comprises a lipid coat.

4. The composition of claim 3 , wherein said particle is a lentivirus.

5. The composition of claim 1 , wherein the amount of said peptide comprising SEQ ID NO:2 in said viral particle is between about 20 and about 250 molecules/μm 2.

6. A pharmaceutical composition comprising:

a viral particle having a radius of less than about 400 nm; and,

at least one peptide comprising SEQ ID NO:2,

wherein said at least one peptide is expressed on an exposed surface of said viral particle; and,

a pharmaceutically acceptable carrier.

7. A method of preparing a viral particle that evades phagocytosis by a phagocytic cell, said method comprising expressing at least one peptide comprising SEQ ID NO:2 on an exposed surface of said viral particle,

whereby said viral particle evades phagocytosis by said phagocytic cell when said viral particle is exposed to said phagocytic cell.

8. A method of increasing the life of a viral particle in vivo in a mammal, said method comprising expressing at least one peptide comprising SEQ ID NO:2 on an exposed surface of said viral particle and administering said viral particle having at least one peptide comprising SEQ ID NO:2 expressed to said mammal,

wherein said administered viral particle has a longer half life in said mammal than an otherwise identical viral particle that does not have at least one peptide comprising SEQ ID NO:2 expressed thereon.

9. The method of claim 8 , wherein said viral particle has a radius of less than about 400 nm.

10. The method of claim 9 , wherein said viral particle has a radius of less than about 150 nm.

11. The method of claim 8 , wherein said viral particle comprises a lipid coat.

12. The method of claim 11 , wherein said viral particle is a lentivirus.

13. The method of claim 8 , wherein the amount of said peptide comprising SEQ ID NO:2 in said viral particle is between about 20 and about 250 molecules/μm 2 .

14. The method of claim 8 , wherein said at least one peptide comprising SEQ ID NO:2 is human CD47.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2010
From: DISCHER, DENNIS E.; TSAI, RICHARD KUO-AN
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 024825/0508 →
Continuity (2)
Provisional Application 61158985 · Mar 10, 2009
Related Publication 20100316570A1 · Dec 16, 2010