IP Library Granted Patent US 9,453,059
Granted Patent B2
US 9,453,059 · App. 13/930,213 · Granted Sep 27, 2016

Immunostimulatory oligonucleotides

Inventors: Heather Davis (Donrobin, CA); Risini Weeratna (Ottawa, CA)
Assignee: Coley Pharmaceutical Group, Inc.
C07K14/47A61K39/00A61K39/0011A61K39/12A61K39/292A61K39/39C07K14/005C07K14/31C12N7/00A61K2039/545A61K2039/55561A61K2039/57C12N2710/16634C12N2730/10134C12N2740/16034C12N2760/18534
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Quick Facts
Patent No.
US 9,453,059
App. No.
13/930,213
Granted
Sep 27, 2016
Kind
B2
Abstract

The invention relates to immunostimulatory oligonucleotides and methods of using immunostimulatory oligonucleotides to induce an antigen-specific immune response. The invention further relates to a vaccine that comprises an immunostimulatory oligonucleotide and an antigen, and comprises a pharmaceutically acceptable carrier. The immunostimulatory oligonucleotides of the invention, in some embodiments, include one or more modified linkage(s).

Claims (24)

1. A composition comprising an antigen and an immunostimulatory oligonucleotide comprising the nucleotide sequence of SEQ ID NO: 1, and further comprising a pharmaceutically acceptable carrier.

2. The composition of claim 1 , wherein the immunostimulatory oligonucleotide is in an effective amount to induce an antigen-specific immune response.

3. The composition of claim 2 , wherein the antigen-specific immune response induced is a Th1 immune response.

4. The composition of claim 1 , wherein the antigen is a microbial antigen, a self antigen or an addictive substance.

5. The composition of claim 4 , wherein the microbial antigen is a bacterial antigen, a viral antigen or a parasitic antigen.

6. The composition of claim 5 , wherein the bacterial antigen is associated with Staphylococcus aureus.

7. The composition of claim 5 , wherein the viral antigen is associated with Respiratory Syncytial virus (RSV), Herpes Simplex virus 1, Herpes Simplex virus 2, Human Immunodeficiency Virus-1 (HIV-1) or HIV-2.

8. The composition of claim 4 , wherein the self antigen is a tumor antigen, an antigen associated with Alzheimer's Disease, an antigen against a human antibody, or an antigen that is expressed from human endogenous retroviral elements.

9. The composition of claim 8 , wherein the tumor antigen is HER2, MAGE, NY-ESO, PSA, CEA or a variant form of EGFR.

10. The composition of claim 8 , wherein the antigen is IgE.

11. The composition of claim 4 , wherein the antigen is a nicotine hapten conjugated to a carrier.

12. The composition of claim 11 , wherein the carrier to which the nicotine hapten is conjugated is diphtheria toxin (DT).

13. The composition of claim 1 , wherein the antigen is a peptide, a recombinant protein, a purified protein, whole killed pathogen, live attenuated virus or viral vector, live attenuated bacteria or a bacterial vector, a polysaccharide, a hapten, or encoded by plasmid DNA.

14. The composition of claim 1 , wherein the antigen is conjugated to a carrier.

15. The composition of claim 14 , wherein the carrier is diphtheria toxin (DT) or a virus-like particle.

16. The composition of claim 15 , wherein the virus-like particle is RNA phage Q-β, hepatitis B surface antigen (HBsAg), or hepatitis B core antigen (HbcAg).

17. The composition of claim 1 , further comprising one or more adjuvants.

18. The composition of claim 17 , wherein the adjuvant is an aluminum salt.

19. The composition of claim 18 , wherein the aluminum salt is aluminum hydroxide.

20. The composition of claim 17 , wherein the adjuvant is a liposome.

21. The composition of claim 1 , wherein the immunostimulatory oligonucleotide comprises one or more phosphorothioate linkages.

22. The composition of claim 1 , wherein the immunostimulatory oligonucleotide comprises at least one lipophilic substituted nucleotide analog and a pyrimidine-purine dinucleotide.

23. The composition of claim 1 , wherein the composition is formulated for administration via a parenteral route, wherein the parenteral route is intramuscular, subcutaneous, intradermal, intravenous or intraperitoneal.

24. The composition of claim 1 , wherein the composition is formulated for administration via a topical route, wherein the topical route is the skin, transdermal or a mucosal surface.

Assignments (1)
ASSIGNEE ADDRESS CORRECTION Recorded Mar 15, 2023
From: COLEY PHARMACEUTICAL GROUP, INC.
To: COLEY PHARMACEUTICAL GROUP, INC.
Reel/Frame 063100/0388 →
Continuity (4)
Division 12632911 · Dec 8, 2009
Provisional Application 61121022 · Dec 9, 2008
Provisional Application 61181799 · May 28, 2009
Related Publication 20150086610A1 · Mar 26, 2015