IP Library Granted Patent US 9,720,000
Granted Patent B2
US 9,720,000 · App. 14/713,721 · Granted Aug 1, 2017

Targeted identification of immunogenic peptides

Inventors: Sathibalan Ponniah (Columbia, MD); George E Peoples (San Antonio, TX); Catherine E Storrer (Columbia, MD); Michael Flora (Mt. Airy, MD)
Assignee: The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc.
G01N33/6803A61K39/0011A61K39/39558C07K16/32C40B30/02G01N33/5011G01N33/564G01N33/574G01N33/577G01N33/6845G01N2500/00G01N2500/04
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Quick Facts
Patent No.
US 9,720,000
App. No.
14/713,721
Granted
Aug 1, 2017
Kind
B2
Abstract

This invention relates generally to identifying peptide sequences involved in antibody binding to any protein for synthesis of vaccine treatments. This novel method allows for a more manageable vaccine peptide discovery and specific generation of unique immunogenic peptides from self-tumor associated proteins and/or foreign proteins from infectious organisms for specific and/or enhanced expression only in the presence of the antibody.

Claims (16)

1. A method of identifying an immunogenic region of a self-protein comprising the steps of:

identifying one or more peptide sequences of a self protein that are directly or indirectly involved with antibody binding, wherein the identifying of the one or more peptide sequences of the self protein comprises: binding an antibody to the self-protein forming a complex; subjecting the complex to proteasome digestion; and obtaining digestion products comprising one or more peptide sequences;

subjecting the one or more peptide sequences to an algorithm that identifies peptide fragments suspected of being immunogenic;

screening all peptide fragments from the one or more peptide sequences for their ability to induce an immune response; and

identifying an immunogenic peptide of the peptide fragment.

2. The method of claim 1 , wherein the antibody binding comprises polyclonal antibody binding.

3. The method of claim 1 , wherein the antibody binding comprises monoclonal antibody binding.

4. The method of claim 1 , further comprising treating a patient with the immunogenic peptide to generate an immune response.

5. The method of claim 1 , wherein the self-protein is HER2/neu.

6. The method of claim 1 , wherein the immune response is a cytotoxic T cell response.

7. The method of claim 1 , wherein screening all peptide fragments from the one or more peptide sequences for their ability to induce an immune response comprises:

stimulating Peripheral Blood Mononuclear Cells with the peptide fragments from the one or more peptide sequences; and

determining the peptide fragments with the highest T cell responses; or

contacting the peptide fragments from the one or more peptide sequences with serum from high risk cancer individuals who do not develop cancer; and

selecting the one or more peptide fragments that bind to the antibodies in the serum; and

determining if the one or more peptide fragments selected in the previous step can induce an antibody response.

Assignments (2)
CONFIRMATORY LICENSE Recorded Oct 27, 2016
From: HENRY M. JACKSON FDN FOR THE ADV MIL/MED
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 040503/0196 →
CONFIRMATORY LICENSE Recorded Jun 15, 2016
From: HENRY M. JACKSON FDN FOR THE ADV MIL/MED
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 039026/0118 →
Continuity (5)
Continuation 13774829 · Feb 22, 2013
Continuation 12045402 · Mar 10, 2008
Continuation PCTUS2006035171 · Sep 8, 2006
Provisional Application 60714865 · Sep 8, 2005
Related Publication 20150260727A1 · Sep 17, 2015