IP Library Granted Patent US 10,556,006
Granted Patent B2
US 10,556,006 · App. 15/717,675 · Granted Feb 11, 2020

Compositions and methods for modulating an immune response

Inventors: Yosef Refaeli (Denver, CO); Brian Curtis Turner (Denver, CO)
Assignee: TAIGA BIOTECHNOLOGIES, INC.
A61K39/39C07K14/001C07K14/47C07K14/82A61K38/00C07K2319/02C07K2319/21
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Quick Facts
Patent No.
US 10,556,006
App. No.
15/717,675
Granted
Feb 11, 2020
Kind
B2
Abstract

Disclosed herein are methods of modulation of the viability of a cell using fusion proteins comprising a transporter peptide sequence and a MYC polypeptide. Further disclosed herein are methods of modulating an immune response using the fusion proteins. Further disclosed herein are methods of identifying agents capable of modulation of the viability of a cell or an immune response. Further disclosed herein are agents and compositions capable of modulation of the viability of a cell or an immune response.

Claims (29)

1. A method of treating a viral infection, comprising administering to an individual in need thereof a fusion peptide comprising:

a. a transporter peptide sequence; and

b. a MYC polypeptide sequence,

wherein the transporter peptide sequence transports the fusion peptide into the nucleus of an immune cell in the individual.

2. The method of claim 1 , wherein the fusion peptide enhances the immune response against the virus.

3. The method of claim 1 , wherein the immune cell is a primary lymphocyte.

4. The method of claim 1 , wherein the individual has a decreased immune response to the virus in the absence of the fusion peptide.

5. The method of claim 1 , wherein the virus is selected from the group consisting of hepatitis A; hepatitis B; polio; measles; mumps; rubella; influenza; varicella zoster virus; rotavirus; smallpox; yellow fever; and human papillomavirus.

6. The method of claim 1 , wherein the virus is an influenza virus.

7. The method of claim 5 , further comprising administering a vaccine for the virus.

8. The method of claim 1 , wherein the fusion peptide has Formula (I):

transporter peptide sequence-MYC sequence.

9. The method of claim 1 , wherein the fusion peptide has Formula (II):

transporter peptide sequence-X-MYC sequence,

wherein —X— is at least one molecule that links the transporter peptide sequence and the MYC sequence.

10. The method of claim 1 , wherein the fusion peptide has Formula (II): transporter peptide sequence-X-MYC sequence, wherein in X is at least one amino acid.

11. The method of claim 1 , wherein the fusion peptide is administered orally, parenterally, intranasally, buccally, rectally, or intravenously.

12. The method of claim 1 , wherein the fusion peptide is administered intramuscularly, subcutaneously, topically or transdermally.

13. The method of claim 1 , wherein the fusion peptide is formulated as a delayed release formulation or as an extended release formulation.

14. A method of increasing an immune response to a virus, comprising administering to an individual that has been exposed to a viral antigen from the virus a fusion peptide comprising:

a. a transporter peptide sequence; and

b. a MYC polypeptide sequence,

wherein the transporter peptide sequence transports the fusion peptide into the nucleus of an immune cell in the individual.

15. The method of claim 14 , wherein the individual has a decreased immune response to the virus in the absence of the fusion peptide.

16. The method of claim 14 , wherein the virus is selected from the group consisting of hepatitis A; hepatitis B; polio; measles; mumps; rubella; influenza; varicella zoster virus; rotavirus; smallpox; yellow fever; and human papillomavirus.

17. The method of claim 16 , wherein the virus is an influenza virus.

18. The method of claim 16 , further comprising administering a vaccine for the virus.

19. The method of claim 14 , wherein the fusion peptide is administered orally, parenterally, intranasally, buccally, rectally, or intravenously.

20. The method of claim 14 , wherein the fusion peptide is administered intramuscularly, subcutaneously, topically or transdermally.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2024
From: TAIGA BIOTECHNOLOGIES (ABC), LLC, AS ASSIGNEE FOR THE BENEFIT OF CREDITORS OF TAIGA BIOTECHNOLOGIES, INC.
To: HTYR ACQUISITION LLC
Reel/Frame 066110/0835 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 3, 2024
From: TAIGA BIOTECHNOLOGIES, INC.
To: TAIGA BIOTECHNOLOGIES (ABC), LLC
Reel/Frame 066186/0624 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 12, 2019
From: REFAELI, YOSEF; TURNER, BRIAN CURTIS
To: TAIGA BIOTECHNOLOGIES, INC.
Reel/Frame 050031/0103 →
Continuity (5)
Continuation 14461105 · Aug 15, 2014
Continuation 13777967 · Feb 26, 2013
Continuation 12550166 · Aug 28, 2009
Provisional Application 61092708 · Aug 28, 2008
Related Publication 20180092972A1 · Apr 5, 2018