IP Library Granted Patent US 9,359,402
Granted Patent B2
US 9,359,402 · App. 14/069,208 · Granted Jun 7, 2016

EphA2 T-cell epitope agonists and uses therefore

Inventors: Walter J. Storkus (Glenshaw, PA); Michael S. Kinch (Laytonsville, MD)
Assignee: UNIVERSITY OF PITTSBURGH—OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
C07K7/06A61K38/1793C07K7/08C07K14/47C07K14/4748C07K14/705G01N33/505G01N33/5091G01N33/56966G01N2333/5409G01N2333/57
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Quick Facts
Patent No.
US 9,359,402
App. No.
14/069,208
Granted
Jun 7, 2016
Kind
B2
Abstract

EphA2 T-cell epitope are provided herein. The epitopes include peptides corresponding to specific fragments of human EphA2 protein containing one or more T-cell epitopes, and conservative derivatives thereof. The EphA2 T-cell epitopes are useful in an assay, such as an ELISPOT assay, that may be used to determine and/or quantify a patient's immune responsiveness to EphA2. The epitopes also are useful in methods of modulating a patient's immune reactivity to EphA2, which has substantial utility as a treatment for cancers that overexpress EphA2, such as renal cell carcinoma (RCC). The EphA2 epitopes also can be used to vaccinate a patient against EphA2, by in vivo or ex vivo methods.

Claims (12)

1. A method of eliciting an immune response to EphA2 in a subject, comprising administering, to the subject, an effective amount of an isolated peptide that consists of 9-35 amino acid residues and wherein said isolated peptide comprises the peptide TLADFDPRV (SEQ ID NO:2, residues 883-891), where said TLADFDPRV (SEQ ID NO:2, residues 883-891) peptide (i) has up to one conservative amino acid substitution within the conservative substitution groups (a) S and T, (b) L, I and V, and (c) E and D; and (ii) retains the ability to stimulate a T-cell immune response to EphA2 as determined by ELISPOT assay.

2. The method of claim 1 , wherein the isolated peptide comprises the peptide TLADFDPRV (SEQ ID NO:2, residues 883-891).

3. The method of claim 1 , where the isolated peptide has one conservative amino acid substitution within the conservative substitution groups (a) S and T, (b) L, I and V, and (c) E and D.

4. A method of eliciting an immune response to EphA2 in a subject, comprising administering, to the subject, an effective amount of a vaccine formulation comprising an isolated peptide that consists of 9-35 amino acid residues and wherein said isolated peptide comprises the peptide TLADFDPRV (SEQ ID NO:2, residues 883-891), where said TLADFDPRV (SEQ ID NO:2, residues 883-891) peptide (i) has up to one conservative amino acid substitution within the conservative substitution groups (a) S and T, (b) L, I and V, and (c) E and D; and (ii) retains the ability to stimulate a T-cell immune response to EphA2 as determined by ELISPOT assay, and a pharmaceutically acceptable carrier.

5. The method of claim 4 where the isolated peptide comprises the peptide TLADFDPRV (SEQ ID NO:2, residues 883-891).

6. The method of claim 4 , where the isolated peptide has one conservative amino acid substitution within the conservative substitution groups (a) S and T, (b) L, I and V, and (c) E and D.

7. The method of claim 4 where the vaccine formulation further comprises an adjuvant.

8. The method of claim 5 where the vaccine formulation further comprises an adjuvant.

9. The method of claim 6 where the vaccine formulation further comprises an adjuvant.

10. The method of claim 4 wherein the isolated peptide comprises a second peptide where said second peptide is not an EphA2 peptide and is immunogenic.

11. The method of claim 5 wherein the isolated peptide comprises a second peptide where said second peptide is not an EphA2 peptide and is immunogenic.

12. The method of claim 6 wherein the isolated peptide comprises a second peptide where said second peptide is not an EphA2 peptide and is immunogenic.

Assignments (1)
CONFIRMATORY LICENSE Recorded Dec 17, 2013
From: UNIVERSITY OF PITTSBURGH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031832/0146 →
Continuity (6)
Division 13355343 · Jan 20, 2012
Division 11977179 · Oct 22, 2007
Continuation 11233796 · Sep 23, 2005
Continuation 10897711 · Jul 22, 2004
Provisional Application 60491046 · Jul 30, 2003
Related Publication 20140134198A1 · May 15, 2014