IP Library Granted Patent US 8,501,417
Granted Patent B2
US 8,501,417 · App. 12/666,566 · Granted Aug 6, 2013

Immunological compositions as cancer biomarkers and/or therapeutics

Inventors: Paula R. Pohlmann (Nashville, TN); Ray Mernaugh (Nashville, TN); Carlos Arteaga (Nashville, TN)
Assignee: Vanderbilt University
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Quick Facts
Patent No.
US 8,501,417
App. No.
12/666,566
Granted
Aug 6, 2013
Kind
B2
Abstract

The present invention concerns antibodies that react immunologically with anti-tumor antigen antibodies and compositions and methods related thereto. In particular, the antibodies that react immunologically with the anti-tumor antigen antibodies are employed in therapeutic, diagnostic, and prognostic embodiments related to cancer, including breast cancer, for example.

Claims (9)

1. A method of determining a response of a subject to an anti-cancer treatment that comprises an anti-tumor antigen antibody, the method comprising:

(a) detecting, in a sample from said subject, an antibody that reacts immunologically with said anti-tumor antigen antibody, and

(b) further treating said subject with said anti-tumor antigen antibody when step (a) reveals the presence of an antibody that reacts immunologically with said anti-tumor antigen antibody.

2. The method of claim 1 , wherein said antibody that reacts immunologically with said anti-tumor antigen antibody is further defined as detecting an anti-idiotypic antibody that reacts immunologically with the variable region of said anti-tumor antigen antibody, wherein the presence of said anti-idiotypic antibody indicates that the subject will respond to said further treatment.

3. The method of claim 1 , wherein the antibody that reacts immunologically with an anti-tumor antigen antibody comprises a polyclonal antibody, a monoclonal antibody, a recombinant ScFv (single chain fragment variable) antibody fragment, Fv, VL or VH fragment, a Fab idiotypic antibody fragment, or an anti-idiotypic antibody fragment.

4. The method of claim 1 , wherein said subject has not previously received said treatment.

5. The method of claim 1 , wherein said subject has previously received said treatment.

6. The method of claim 1 , wherein said tumor antigen comprises HER2, (EGFR) HER1. HER3, HER4, VEGFR, CD20, or EpCAM.

7. The method of claim 1 , wherein said anti-tumor antigen antibody comprises trastuzumab, cetuximab, rituximab, bevacizumab, edrecolomab, panitumumab or alemtuzumab.

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 20, 2010
From: VANDERBILT UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024258/0577 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 22, 2010
From: POHLMANN, PAULA R.; ARTEAGA, CARLOS; MERNAUGH, RAY
To: VANDERBILT UNIVERSITY
Reel/Frame 024112/0319 →
Continuity (2)
Provisional Application 60946295 · Jun 26, 2007
Related Publication 20100215647A1 · Aug 26, 2010