IP Library Granted Patent US 10,314,906
Granted Patent B2
US 10,314,906 · App. 15/558,942 · Granted Jun 11, 2019

Virus-like particle compositions and vaccines against Epstein-Barr virus infection and disease

Inventors: Javier Gordon Ogembo (North Grafton, MA); Trudy Morrison (Northborough, MA)
Assignee: University of Massachusetts
A61K39/245A61K39/12C12N7/00G01N33/574A61K2039/5256A61K2039/5258A61K2039/575A61K2039/585A61K2039/70C12N2710/16222C12N2710/16223C12N2710/16234C12N2710/16271C12N2710/20022C12N2710/20023C12N2710/20034C12N2710/20071C12N2760/18122C12N2760/18123C12N2760/18134C12N2760/18171G01N2333/05
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Quick Facts
Patent No.
US 10,314,906
App. No.
15/558,942
Granted
Jun 11, 2019
Kind
B2
Abstract

The present inaveation relates to prophylactic and/or therapeutic vaccines thatpoatairj Newcastle disease Virus (NDV) virus-like particles (VLPs) comprising one or more Epstein-Barr Virus (EBV) antigens, in one embodiment, the invention provides a recombinant virus-like particle (V'UP) comprising, i is operable combination, a) Newcastle disease virusΛ iNDVj matrix (M) protein, and b) one or more Epstein-Barr Virus (BBV) antigens. The im'eniion's prophylactic and/or therapeutic vacclrses are useful for preventing asc/or treatmg, infection with EBY aixi/or disease associated Epstein-Barr Virus, such as cancer.

Claims (31)

1. A recombinant virus-like particle (VLP) comprising, in operable combination,

a) Newcastle disease virus (NDV) matrix (M) protein,

b) NDV nucleocapsid (NP) protein, and

c) one or more tumor-associated EBV antigen,

wherein said one or more tumor-associated EBV antigen is fused to the C-terminal end of said NDV NP protein and is inside said VLP.

2. The VLP of claim 1 , wherein said tumor-associated EBV antigen is selected from the group consisting of EBNA1, tEBNA1 and LMP2.

3. The VLP of claim 1 , wherein said tumor-associated EBV antigen comprises tEBNA1 and LMP2.

4. The VLP of claim 3 , further comprising, in operable combination, one or more Epstein-Barr Virus (EBV) antigens, wherein at least one of said one or more antigens is selected from the group consisting of gB, gH, and gL.

5. The VLP of claim 3 , wherein said VLP further comprises, in operable combination, EBV gp350/220.

6. The VLP of claim 3 , wherein said VLP further comprises, in operable combination, one or more NDV proteins.

7. The VLP of claim 6 , wherein said one or more NDV proteins comprise NDV heptad repeat domain 2 (HR2) protein.

8. The VLP of claim 7 , wherein said one or more NDV proteins comprise NDV fusion (F) protein.

9. The VLP of claim 8 , wherein said one or more NDV proteins comprise NDV heamagglutinin-neuraminidase (HN) protein.

10. The VLP of claim 1 , further comprising, in operable combination, one or more human papillomavirus antigens.

11. The VLP of claim 10 , wherein said one or more human papillomavirus antigens comprises one or more of L1 and L2.

12. A vaccine comprising the VLP of claim 1 and a physiologically acceptable carrier.

13. An expression vector encoding the recombinant VLP of claim 1 .

14. A method for immunizing a mammalian subject against cancer, comprising administering an immunologically effective amount of one or more vaccine of claim 12 to a mammalian subject in need thereof to produce a treated subject, wherein said administering is under conditions to produce an immune response to one or more tumor-associated EBV antigen.

15. The method of claim 14 , wherein said cancer comprises an Epstein-Barr Virus (EBV) associated cancer.

16. The method of claim 14 , wherein said EBV-associated cancer comprises nasopharyngeal carcinoma.

17. The method of claim 14 , wherein said immune response comprises T lymphocytes that specifically bind to said one or more tumor-associated EBV antigen.

18. The method of claim 17 , wherein said immune response lacks antibody that specifically binds to said one or more tumor-associated EBV antigen.

19. The method of claim 17 , wherein said T lymphocytes are selected from CD4 + lymphocytes and CD8 + lymphocytes.

20. The method of claim 14 , wherein said method further comprises administering a recombinant VLP that contains, in operable combination,

a) Newcastle disease virus (NDV) matrix (M) protein, and

b) EBV gp350/220.

21. The method of claim 14 , wherein said method further comprises one or more of

a) detecting said immune response to said one or more tumor-associated EBV antigen, and

b) detecting a reduction in one or more symptoms of said cancer in said treated subject.

22. The method of claim 14 , wherein said administering is before manifestation of one or more symptoms of said cancer.

23. The method of claim 14 , wherein said administering is after manifestation of one or more symptoms of said cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2019
From: OGEMBO, JAVIER GORDON; MORRISON, TRUDY
To: UNIVERSITY OF MASSACHUSETTS
Reel/Frame 047927/0478 →
Continuity (2)
Provisional Application 62134785 · Mar 18, 2015
Related Publication 20180078634A1 · Mar 22, 2018
Cited By (5)
US 12,303,559 US 12,319,938 US 12,351,814 US 12,351,815 US 12,404,525