IP Library Granted Patent US 9,814,767
Granted Patent B2
US 9,814,767 · App. 14/379,150 · Granted Nov 14, 2017

Methods and materials for generating CD8+ T cells having the ability to recognize cancer cells expressing a HER2/neu polypeptide

Inventors: Keith L. Knutson (Fort Pierce, FL); Andrea M. Henle (Cambridge, MA)
Assignee: Mayo Foundation for Medical Education and Research
A61K39/0011A61K45/06C07K14/71A61K2039/55566
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Quick Facts
Patent No.
US 9,814,767
App. No.
14/379,150
Granted
Nov 14, 2017
Kind
B2
Abstract

This document provides methods and materials for generating CD8 + T cells having the ability to recognize cancer cells expressing a HER2/neu polypeptide. For example, methods and materials for using a polypeptide consisting of an SLAFLPESFD amino acid sequence in vivo or in vitro to generate CD8 + T cells having the ability to recognize and lyse cancer cells expressing a HER2/neu polypeptide are provided.

Claims (15)

1. A composition comprising a polypeptide, wherein the sequence of said polypeptide consists of the amino acid sequence set forth in SEQ ID NO:1, wherein said polypeptide is immunogenic, and wherein said composition comprises an adjuvant and an agent selected from the group consisting of IL-2, GM-CSF, and rintatolimod.

2. The composition of claim 1 , wherein said adjuvant is an oil and water mixture.

3. The composition of claim 1 , wherein said adjuvant is Montanide ISA-51.

4. The composition of claim 1 , wherein said agent is IL-2.

5. A method for increasing the number of CD8 + T cells having the ability to kill breast cancer cells expressing a HER2/neu polypeptide, wherein said method comprises contacting a population of CD8 + T cells with a polypeptide and an agent selected from the group consisting of IL-2, GM-CSF, and rintatolimod, wherein the sequence of said polypeptide consists of the amino acid sequence set forth in SEQ ID NO:1.

6. The method of claim 5 , wherein said contacting step occurs in an ex vivo manner.

7. The method of claim 5 , wherein said contacting step occurs in an in vivo manner.

8. A method for increasing, within a human, the number of CD8 + T cells having the ability to kill breast cancer cells expressing a HER2/neu polypeptide, wherein said method comprises administering a composition to said human, wherein said composition comprises a polypeptide and an agent selected from the group consisting of IL-2, GM-CSF, and rintatolimod, wherein the sequence of said polypeptide consists of the amino acid sequence set forth in SEQ ID NO:1.

9. The method of claim 8 , wherein said human contains breast cancer cells expressing said HER2/neu polypeptide.

10. The method of claim 8 , wherein said composition comprises an adjuvant.

11. The method of claim 10 , wherein said adjuvant is an oil and water mixture.

12. The method of claim 10 , wherein said adjuvant is Montanide ISA-51.

13. The method of claim 8 , wherein said agent is IL-2.

14. The method of claim 8 , wherein said agent is GM-CSF.

15. The method of claim 8 , wherein said method further comprises administering trastuzumab to said human.

Assignments (3)
CONFIRMATORY LICENSE Recorded Jan 5, 2015
From: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 034719/0795 →
CONFIRMATORY LICENSE Recorded Oct 28, 2014
From: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 034068/0581 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2014
From: KNUTSON, KEITH L.; HENLE, ANDREA M.
To: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
Reel/Frame 033900/0230 →
Continuity (2)
Provisional Application 61600480 · Feb 17, 2012
Related Publication 20150231218A1 · Aug 20, 2015