IP Library Granted Patent US 8,927,288
Granted Patent B2
US 8,927,288 · App. 14/092,412 · Granted Jan 6, 2015

Phage antibodies to radiation-inducible neoantigens

Inventors: Dennis E. Hallahan (St. Louis, MO); Raymond Mernaugh (Franklin, TN)
Assignee: Vanderbilt University
A61K51/1203A61K51/1255C07K16/2848A61K2039/505A61B8/481C07K16/30G01N33/6854C07K16/2854A61B6/481C07K2317/622A61K41/0038G01R33/281C07K2317/34A61B5/0071A61N5/10C12Q1/6886C12Q1/6809A61K41/00
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Quick Facts
Patent No.
US 8,927,288
App. No.
14/092,412
Granted
Jan 6, 2015
Kind
B2
Abstract

A method for identifying a molecule that binds an irradiated tumor in a subject and molecules identified thereby. The method includes the steps of: (a) exposing a tumor to ionizing radiation; (b) administering to a subject a library of diverse molecules; and (c) isolating from the tumor one or more molecules of the library of diverse molecules, whereby a molecule that binds an irradiated tumor is identified. Also provided are therapeutic and diagnostic methods using targeting ligands that bind an irradiated tumor.

Claims (9)

1. A method of targeting a therapeutic agent to a target tissue, the method comprising: (a) providing an immunoconjugate composition comprising a single chain fragment variable (scFv) antibody that binds to a radiation-inducible neoantigen selected from the group consisting of P-selectin, E-selectin, endoglin, α 2b β 3 integrin and α v β 3 integrin, or a Fab fragment thereof, conjugated to a therapeutic agent, wherein the immunoconjugate composition is capable of binding to a radiation-inducible neoantigen; (b) irradiating the target tissue to induce expression of the radiation-inducible neoantigen in the target tissue; and (c) contacting the irradiated target tissue with the immunoconjugate composition under conditions sufficient for binding of the antibody or antibody fragment to the radiation-inducible neoantigen, whereby the therapeutic agent is targeted to the target tissue.

2. The method of claim 1 , wherein the immunoconjugate is administered to the subject in a pharmaceutically acceptable carrier.

3. The method of claim 1 , wherein the therapeutic agent is selected from the group consisting of a virus, a radionuclide, a cytotoxin, a therapeutic gene, and a chemotherapeutic agent.

4. The method of claim 1 , wherein the single chain fragment variable (scFv) antibody or Fab antibody is humanized.

5. The method of claim 1 , wherein the immunoconjugate is polyvalent.

6. The method of claim 1 , further comprising a detectable label.

7. The method of claim 1 , wherein the detectable label comprises a label that can be detected using magnetic resonance imaging, scintigraphic imaging, ultrasound, or fluorescence.

8. The method of claim 7 , wherein the label that can be detected using scintigraphic imaging comprises a radionuclide label.

9. The method of claim 8 , wherein the radionuclide label comprises 131 I or 99 mTc.

Assignments (3)
CONFIRMATORY LICENSE Recorded Jul 13, 2016
From: WASHINGTON UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039321/0527 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2014
From: HALLAHAN, DENNIS
To: VANDERBILT UNIVERSITY
Reel/Frame 032807/0393 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2014
From: MERNAUGH, RAYMOND
To: VANDERBILT UNIVERSITY
Reel/Frame 032815/0445 →
Continuity (6)
Division 13195570 · Aug 1, 2011
Division 11953780 · Dec 10, 2007
Division 10689006 · Oct 20, 2003
Continuation In Part 09914605 · Nov 9, 2001
Continuation In Part 10259087 · Sep 27, 2002
Related Publication 20140088408A1 · Mar 27, 2014