IP Library Granted Patent US 8,658,168
Granted Patent B2
US 8,658,168 · App. 10/118,262 · Granted Feb 25, 2014

Compositions and methods for homoconjugates of antibodies which induce growth arrest of apoptosis of tumor cells

Inventors: Maria-Ana Ghetie (Dallas, TX); Jonathan W. Uhr (Dallas, TX); Ellen S. Vitetta (Dallas, TX)
Assignee: The Board of Regents of The University of Texas System
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Quick Facts
Patent No.
US 8,658,168
App. No.
10/118,262
Granted
Feb 25, 2014
Kind
B2
Abstract

This invention discloses monoclonal antibodies (MAbs) which have little or no signaling activity as monomers become potent anti-tumor agents when they are converted into homoconjugates. The homoconjugates exert anti-growth activity by signaling G 0 /G 1 arrest or apoptosis, depending upon which cell surface molecule they bind. This activity is specific and does not require an Fc portion. These conjugates are potent, anti-tumor agents.

Claims (11)

1. A method of treating a neoplastic cell comprising:

obtaining a chemically engineered or recombinantly engineered conjugate of two or more monoclonal antibodies, wherein the conjugate comprises an anti-CD19, anti-CD20, anti-CD21, anti-CD22, anti-breast tumor, anti-ovarian tumor, anti-prostate tumor, anti-lung tumor, or anti-αHer2 monoclonal antibody that does not comprise an Fc region and wherein the conjugate comprises an anti-CD19, anti-CD20, anti-CD21, anti-CD22, anti-breast tumor, anti-ovarian tumor, anti-prostate tumor, anti-lung tumor, or anti-αHer2 monoclonal antibody that has anti-neoplastic activity in a conjugated form and has substantially no anti-neoplastic activity in an unconjugated form; and

contacting a neoplastic cell with the conjugate, wherein the conjugate directly signals growth arrest or apoptosis in the cell.

2. The method of claim 1 , wherein the anti-neoplastic activity comprises growth arrest.

3. The method of claim 1 , wherein the conjugate is a homoconjugate.

4. The method of claim 3 , wherein the homoconjugate is an anti-CD19 homoconjugate.

5. The method of claim 1 , wherein the conjugate comprises a monoclonal antibody that is an IgG monomer.

6. The method of claim 1 , wherein no monoclonal antibody in the conjugate comprises an Fc region.

7. The method of claim 1 , wherein the conjugate comprises an anti-CD19, anti-CD20, anti-CD21, anti-CD22, or anti-αHer2 monoclonal antibody that does not comprise an Fc region and wherein the conjugate comprises an anti-CD19, anti-CD20, anti-CD21, anti-CD22, or anti-αHer2 monoclonal antibody that has anti-neoplastic activity in a conjugated form and has substantially no anti-neoplastic activity in an unconjugated form.

8. The method of claim 1 , wherein the neoplastic cell is contacted in vitro.

9. The method of claim 1 , wherein the neoplastic cell is contacted in vivo.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2013
From: GHETIE, MARIA-ANA; UHR, JOHNATHAN W.; VITETTA, ELLEN S.
To: THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 031520/0037 →
CONFIRMATORY LICENSE Recorded Dec 16, 2009
From: THE UNIVERSITY OF TEXAS SYSTEM
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 023659/0040 →
Continuity (4)
Division 09112041 · Jul 8, 1998
Provisional Application 60052013 · Jul 8, 1997
Related Publication 20030165509A1 · Sep 4, 2003
Related Publication 20060099213A9 · May 11, 2006