IP Library Granted Patent US 9,321,992
Granted Patent B2
US 9,321,992 · App. 10/461,887 · Granted Apr 26, 2016

Cell targeting methods and compositions

Inventors: James E. Dennis (Cleveland Heights, OH); Arnold I. Caplan (Cleveland Heights, OH); Nir Cohen (Tel Aviv, IL)
Assignee: Case Western Reserve University
C12N5/0655C07K16/18C12N5/0006A61K35/12
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Quick Facts
Patent No.
US 9,321,992
App. No.
10/461,887
Granted
Apr 26, 2016
Kind
B2
Abstract

In certain aspects, the invention relates to cell delivery compositions comprising a chondrogenic cell and a targeting moiety. Such compositions may be used, for example, in administering a targeted cell therapy to a subject.

Claims (33)

1. A composition for targeting a chondrogenic cell to a cartilage matrix comprising:

a chondrogenic cell; and

a targeting moiety that binds to an epitope of cartilage matrix, said targeting moiety being selected from the group consisting of an antibody and an antibody fragment;

wherein said chondrogenic cell is linked to said targeting moiety, and

wherein the linked targeting moiety enhances adherence of the chondrogenic cell to cartilage matrix when administered to a cartilage matrix injury site and wherein the linked targeting moiety does not adversely affect chondrogenic cell viability, mitotic potential, and phenotype.

2. The composition of claim 1 , wherein said antibody is a monoclonal antibody.

3. The composition of claim 1 , wherein said antibody is a polyclonal antibody.

4. The composition of claim 1 , wherein said antibody is selected from the group consisting of anti-collagen type II, anti-chondroitin 4-sulfate and anti-keratan sulfate.

5. The composition of claim 1 , wherein said antibody is modified with a hydrophobic moiety.

6. The composition of claim 5 , wherein said hydrophobic moiety is a palmitoyl moiety.

7. The composition of claim 5 , wherein said hydrophobic moiety is a myristoyl moiety.

8. The composition of claim 1 , wherein said antibody fragment is selected from the group consisting of Fv fragment, single chain Fv (scFv) fragment, Fab′ fragment, F(ab′)2 fragment, single domain antibody, camelized antibody, humanized antibody, diabodies, tribodies, and tetrabodies.

9. The composition of claim 1 , wherein said chondrogenic cell is linked to said targeting moiety directly.

10. The composition of claim 1 , wherein said chondrogenic cell is linked to said targeting moiety via a linker.

11. The composition of claim 10 , wherein said linker is selected from the group consisting of protein G and protein A.

12. A composition for targeting a chondrogenic cell to a cartilage matrix comprising:

a chondrogenic cell; and

an antibody that binds to an of epitope of cartilage matrix, the antibody being selected from the group consisting of anti-collagen type II antibodies, anti-chondroitin 4-sulfate antibodies, and anti-keratan sulfate antibodies;

wherein said chondrogenic cell is linked to said antibody by a palmitoyl moiety, and wherein the linked antibody enhances adherence of the chondrogenic cell to cartilage matrix when administered to a cartilage matrix injury site and does not adversely affect chondrogenic cell viability, mitotic potential, and chondrogenic phenotype.

13. The composition of claim 12 , wherein said antibody is a monoclonal antibody.

14. The composition of claim 12 , wherein said antibody is a polyclonal antibody.

15. The composition of claim 12 , wherein said antibody is selected from the group consisting of Fv fragment, single chain Fv (scFv) fragment, Fab′ fragment, F(ab′)2 fragment, single domain antibody, camelized antibody, humanized antibody, diabodies, tribodies, and tetrabodies.

16. A composition for targeting a chondrogenic cell to a cartilage matrix comprising:

a chondrogenic cell;

a first antibody that binds to an epitope of cartilage matrix, the first antibody comprising an anti-collagen type II antibody;

a second antibody that binds to an epitope of cartilage matrix, the second antibody comprising an anti-chondroitin 4-sulfate antibody;

wherein said chondrogenic cell is linked to the antibodies by a palmitoyl moiety, and wherein the linked antibodies enhance adherence of the chondrogenic cell to cartilage matrix when administered to a cartilage matrix injury site and do not adversely affect chondrogenic cell viability, mitotic potential, and chondrogenic phenotype.

17. A composition for targeting a chondrogenic cell to a cartilage matrix comprising:

a chondrogenic cell;

a first antibody that binds to an epitope of cartilage matrix, the first antibody comprising an anti-collagen type II antibody;

a second antibody that binds to an epitope of cartilage matrix, the second antibody comprising an anti-chondroitin 4-sulfate antibody; and

a third antibody that binds to an epitope of cartilage matrix, the third antibody comprising an anti-keratan sulfate antibody;

wherein said chondrogenic cell is linked to the antibodies by a palmitoyl moiety, and wherein the linked antibodies enhance adherence of the chondrogenic cell to cartilage matrix when administered to a cartilage matrix injury site and do not adversely affect chondrogenic cell viability, mitotic potential, and chondrogenic phenotype.

Assignments (4)
CONFIRMATORY LICENSE Recorded Aug 15, 2010
From: CASE WESTERN RESERVE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024837/0747 →
CONFIRMATORY LICENSE Recorded Jun 4, 2009
From: CASE WESTERN RESERVE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022779/0245 →
CONFIRMATORY LICENSE Recorded Oct 1, 2008
From: CASE WESTERN RESERVE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021615/0962 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2003
From: CAPLAN, ARNOLD; DENNIS, JAMES; COHEN, NIR
To: CASE WESTERN RESERVE UNIVERSITY
Reel/Frame 014136/0046 →
Continuity (2)
Provisional Application 60389079 · Jun 14, 2002
Related Publication 20040048370A1 · Mar 11, 2004