CMV vectors comprising microRNA recognition elements

Patent metadata

Field	Value
Publication number	US-10688164-B2
Application number	US-201615356627-A
Country	US
Kind code	B2
Filing date	Nov 20, 2016
Priority date	Nov 20, 2015
Publication date	Jun 23, 2020
Grant date	Jun 23, 2020

Abstract

Disclosed herein are recombinant CMV vectors comprising heterologous antigens and microRNA recognition elements to silence expression of CMV genes in the presence of microRNA derived from myeloid cells, an active UL128 protein and an active UL130 protein. Also disclosed are recombinant CMV vectors comprising heterologous antigens and microRNA recognition elements to silence expression of CMV genes in the presence of microRNA derived from myeloid cells, an inactive UL128 protein and an inactive UL130 protein. Also disclosed are methods of generating an unconventional immune response using these vectors. Such an immune response is characterized by generation of a CD8+ T cell response that is predominantly restricted by MHC-II.

First claim

What is claimed is:

1. A method of generating an immune response to at least one heterologous antigen in a subject, the method comprising administering to the subject a cytomegalovirus (CMV) vector in an amount effective to elicit a CD8+ T cell response to the at least one heterologous antigen in the subject, wherein the CMV vector comprises:
(a) a first nucleic acid sequence encoding at least one heterologous antigen;
(b) a second nucleic acid sequence comprising a first microRNA recognition element (MRE) operably linked to a CMV gene that is essential or augmenting for CMV growth and wherein the MRE silences expression in presence of miR-142-3p;
(c) a third nucleic acid sequence that encodes an active UL128 protein or ortholog thereof; and
(d) a fourth nucleic acid sequence that encodes an active UL130 protein or ortholog thereof.

2. The method of claim 1 , wherein at least 10% of the CD8+ T cells elicited by the CMV vector are restricted by Class II MHC or an ortholog thereof.

3. The method of claim 2 , wherein at least 20% of the CD8+ T cells are restricted by Class II MHC or an ortholog thereof.

4. The method of claim 3 , wherein fewer than 10% of the CD8+ T cells are restricted by MHC-E or an ortholog thereof.

5. The method of claim 2 , wherein at least 30% of the CD8+ T cells are restricted by Class II MHC or an ortholog thereof.

6. The method of claim 2 , wherein at least 40% of the CD8+ T cells are restricted by Class II MHC or an ortholog thereof.

7. The method of claim 2 , wherein at least 50% of the CD8+ T cells are restricted by Class II MHC or an ortholog thereof.

8. The method of claim 2 , wherein at least 60% of the CD8+ T cells are restricted by Class II MHC or an ortholog thereof.

9. The method of claim 2 , wherein at least 75% of the CD8+ T cells are restricted by Class II MHC or an ortholog thereof.

10. The method of claim 1 , wherein the subject has been previously exposed to CMV.

11. The method of claim 1 , wherein the subject is a human or nonhuman primate.

12. The method of claim 1 , wherein administering the CMV vector comprises subcutaneous, intravenous, intramuscular, intraperitoneal, or oral administration of the CMV vector.

13. The method of claim 1 , wherein the first MRE of the CMV vector silences expression of IE2 or an ortholog thereof in the presence of miR-142-3p.

14. The method of claim 1 , wherein the first MRE of the CMV vector silences expression of UL79 or an ortholog thereof in the presence of miR-142-3p.

15. The method of claim 1 , wherein the CMV vector further comprises a second MRE operably linked to a CMV gene that is essential or augmenting for CMV growth, and wherein the second MRE silences expression in the presence of miR-142-3p.

16. The method of claim 15 , wherein the first MRE of the CMV vector silences expression of IE2 or an ortholog thereof in the presence of miR-142-3p, and wherein the second MRE of the CMV vector silences expression of UL79 or an ortholog thereof in the presence of miR-142-3p.

17. The method of claim 1 , wherein the at least one heterologous antigen comprises a pathogen-specific antigen, a tumor antigen, a tissue-specific antigen, or a host self-antigen.

18. The method of claim 17 , wherein the pathogen specific antigen is derived from human immunodeficiency virus, simian immunodeficiency virus, herpes simplex virus, hepatitis B virus, hepatitis C virus, papillomavirus, Plasmodium parasites, or Mycobacterium tuberculosis.

19. The method of claim 17 , wherein the tumor antigen is related to acute myelogenous leukemia, chronic myelogenous leukemia, myelodysplastic syndrome, acute lymphoblastic leukemia, chronic lymphoblastic leukemia, non-Hodgkin's lymphoma, multiple myeloma, malignant melanoma, breast cancer, lung cancer, ovarian cancer, prostate cancer, pancreatic cancer, colon cancer, renal cell carcinoma (RCC), or germ cell tumors.

20. The method of claim 1 , wherein the CMV vector does not express an active UL79 protein or an ortholog thereof.

21. The method of claim 1 , wherein the CMV vector does not express an active UL82 (pp71) protein or an ortholog thereof.

22. The method of claim 1 , wherein the CMV vector does not express an active US11 protein or an ortholog thereof.

23. The method of claim 1 , where the CMV vector (a) does not express an active UL79 protein or an ortholog thereof, (b) does not express an active UL82 (pp71) protein or an ortholog thereof, and (c) does not express an active US11 protein or an ortholog thereof.

Assignees

• Univ Oregon Health & Science

Inventors

• Nelson Jay
• Hansen Scott
• Hancock Meaghan H
• Picker Louis
• Frueh Klaus

Classifications

• Y02A50/30

  Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change · CPC title

• A61K39/12 Primary

  Viral antigens · CPC title

• A61K39/00 Primary

  Medicinal preparations containing antigens or antibodies (materials for immunoassay G01N33/53) · CPC title

• C12N2710/16162

  by genetic engineering · CPC title

• C12N2710/16143

  viral genome or elements thereof as genetic vector · CPC title