IP Library Granted Patent US 10,414,813
Granted Patent B2
US 10,414,813 · App. 15/548,749 · Granted Sep 17, 2019

Minor histocompatibility antigens and uses thereof

Inventors: Claude Perreault (Québec, CA); Diana Paola Granados (Québec, CA); Jean-Sébastien Delisle (Québec, CA); Pierre Thibault (Québec, CA); Sébastien Lemieux (Québec, CA)
Assignees: UNIVERSITÉ DE MONTRÉAL; RSEM, LIMITED PARTNERSHIP
C07K14/70539A61K35/13A61K35/17A61K39/0011C07K1/047C07K7/06C07K7/08A61K39/00A61K2035/124A61K2039/505A61K2039/5158C07K2319/02G01N2333/70539
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Quick Facts
Patent No.
US 10,414,813
App. No.
15/548,749
Granted
Sep 17, 2019
Kind
B2
Abstract

Novel minor histocompatibility antigens (MiHAs) are described. These novel MiHAs were selected based on two features: (i) they are encoded by loci with a minor allele frequency (MAF) of at least 0.05; and (ii) they have adequate tissue distribution. Compositions, nucleic acids and cells related to these novel MiHAs are also described. The present application also discloses the use of these novel MiHAs, and related compositions, nucleic acids and cells, in applications related to cancer immunotherapy, for example for the treatment of hematologic cancers such as leukemia.

Claims (18)

1. A method of treating cancer, said method comprising administering to a subject expressing a major histocompatibility complex (MHC) class I molecules of the HLA-A*02:01 allele in need thereof an effective amount of CD8 + T lymphocytes recognizing a MHC class I molecule of the HLA-A*02:01 allele loaded with a minor histocompatibility antigen (MiHA) peptide of 8 to 14 amino acids comprising the sequence (i) HLEEQIAKV (SEQ ID NO: 5) if said subject expresses the sequence HLEEQIAKV (SEQ ID NO: 5), or (ii) HLEEQIPKV (SEQ ID NO: 6) if said subject expresses the sequence HLEEQIPKV (SEQ ID NO: 6).

2. The method of claim 1 , wherein said subject in need thereof is an allogeneic stem cell transplantation (ASCT) recipient.

3. The method of claim 1 , wherein said cancer is a hematologic cancer.

4. The method of claim 3 , wherein said hematologic cancer is leukemia.

5. The method of claim 1 , wherein said CD8 T lymphocytes are ex vivo expanded primary CD8 T lymphocytes or CD8 T lymphocyte clones expressing a recombinant T cell receptor (TCR).

6. The method of claim 1 , wherein said method further comprises administering an effective amount of the MiHA peptide recognized by said CD8 + T lymphocytes, and/or (ii) an antigen-presenting cell (APC) expressing at its surface MHC class I molecules comprising the MiHA peptide in their peptide binding groove.

7. The method of claim 1 , wherein said method further comprises culturing and expanding said CD8 T lymphocytes in the presence of cells expressing said MHC class I molecule loaded with said MiHA peptide in vitro prior to administration to the subject, and wherein said CD8 T lymphocytes are from a second subject that does not express said MiHA peptide.

8. The method of claim 7 , wherein said subject is an allogeneic stem cell transplantation (ASCT) recipient.

9. The method of claim 7 , wherein said cancer is a hematologic cancer.

10. The method of claim 9 , wherein said hematologic cancer is leukemia.

11. The method of claim 7 , wherein said method further comprises administering an effective amount of the MiHA peptide defined in claim 1 , and/or (ii) an antigen-presenting cell (APC) expressing at its surface MHC class I molecules comprising the MiHA peptide in their peptide binding groove.

12. The method of claim 1 , wherein said MiHA peptide consists of the sequence HLEEQIA/PKV (SEQ ID NO: 4).

13. The method of claim 12 , wherein said subject is an allogeneic stem cell transplantation (ASCT) recipient.

14. The method of claim 13 , wherein said cancer is a hematologic cancer.

15. The method of claim 14 , wherein said hematologic cancer is leukemia.

16. The method of claim 12 , wherein said CD8 T lymphocytes are ex vivo expanded primary CD8 T lymphocytes or CD8 T lymphocyte clones expressing a recombinant T cell receptor (TCR).

17. The method of claim 12 , wherein said method further comprises administering an effective amount of the MiHA peptide recognized by said CD8 + T lymphocytes, and/or (ii) an antigen-presenting cell (APC) expressing at its surface MHC class I molecules comprising the MiHA peptide in their peptide binding groove.

18. The method of claim 12 , wherein said method further comprises culturing and expanding said CD8 T lymphocytes in the presence of cells expressing said MHC class I molecule loaded with said MiHA peptide in vitro prior to administration to the subject, and wherein said CD8 T lymphocytes are from a second subject that does not express said MiHA peptide.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2017
From: PERREAULT, CLAUDE; GRANADOS, DIANA PAOLA; LEMIEUX, SÉBASTIEN; THIBAULT, PIERRE
To: UNIVERSITÉ DE MONTRÉAL
Reel/Frame 043201/0666 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2017
From: DELISLE, JEAN-SÉBASTIEN
To: HÔPITAL MAISONNEUVE-ROSEMONT
Reel/Frame 043201/0718 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2017
From: HÔPITAL MAISONNEUVE-ROSEMONT
To: RSEM, LIMITED PARTNERSHIP
Reel/Frame 043201/0738 →
Continuity (2)
Provisional Application 62113727 · Feb 9, 2015
Related Publication 20180030112A1 · Feb 1, 2018