IP Library Granted Patent US 7,255,868
Granted Patent B2
US 7,255,868 · App. 10/176,883 · Granted Aug 14, 2007

Chimeric immunomodulatory compounds and methods of using the same—I

Assignee: Dynavax Technologies Corporation
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Quick Facts
Patent No.
US 7,255,868
App. No.
10/176,883
Granted
Aug 14, 2007
Kind
B2
Abstract

The invention provides immunomodulatory compounds and methods for immunomodulation of individuals using the immunomodulatory compounds.

Claims (54)

1. A chimeric immunostimulatory compound (CIC) comprising the structure N 1 -S 1 -N 2 -N 3 ,

wherein N 1 , N 2 , and N 3 are independently selected nucleic acid moieties comprising 3 to 7 bases, at least one of N 1 , N 2 , and N 3 has the sequence 5′-[(X) 0-2 ]TCG[(X) 2-4 ]-3′, wherein each X is an independently selected nucleotide;

wherein S 1 is a non-nucleic acid spacer moiety covalently bound to N 1 and N 2 ; S 2 is a non-nucleic acid spacer moiety covalently bound to N 2 and N 3 ; S 1 and S 2 are the same or different; each of S 1 and S 2 comprises hexaethylene glycol (HEG), triethylene glycol (TEG), propyl, or butyl; and

wherein said CIC has at least one immunostimulatory activity selected from the group consisting of (i) the ability to stimulate interferon-gamma (IFN-γ) production by human peripheral blood mononuclear cells and (ii) the ability to stimulate interferon-alpha (IFN-α) production by human peripheral blood mononuclear cells.

2. The CIC of claim 1 wherein at least one of S 1 and S 2 is a HEG spacer moiety.

3. The CIC of claim 2 wherein both S 1 and S 2 are HEG spacer moieties.

4. The CIC of claim 1 wherein at least one of N 1 and N 3 has a sequence 5′-TCG[(X) 2-4 ]-3′.

5. The CIC of claim 1 wherein at least one of N 1 and N 3 has a sequence 5′-TCG(A/T)[(X) 1-3 ]-3′.

6. The CIC of claim 5 wherein at least one of N 1 and N 3 has a sequence 5′-TCG(A/T)CG(A/T)-3′.

7. The CIC of claim 6 wherein at least one nucleic acid moiety comprises the sequence 5′-TCGACGT-3′ or 5′-TCGTCGA-3′.

8. The CIC of claim 3 wherein at least one of N 1 and N 3 has a sequence 5′-TCG(A/T)[(X) 1-3 ]-3′.

9. The CIC of claim 8 wherein at least one of N 1 and N 3 has a sequence 5′-TCG(A/T)CG(A/T)-3′.

10. The CIC of claim 9 wherein at least one nucleic acid moiety comprises the sequence 5′-TCGACGT-3′ or 5′-TCGTCGA-3′.

11. The CIC of claim 1 , where the linkages between nucleotides of the nucleic acid moieties and between the nucleic acid moieties and the nonnucleic acid spacer moieties comprise one or more linkages selected from the group consisting of phosphodiester linkages, phosphorothioate ester linkages, and phosphorodithioate ester linkages.

12. A composition comprising a CIC of claim 1 and a pharmaceutically acceptable excipient.

13. A composition comprising a CIC of claim 1 and further comprising an antigen.

14. A composition comprising a CIC of claim 1 and further comprising a cationic microsphere.

15. The composition of claim 14 wherein the microsphere comprises a polymer of lactic acid and glycolic acid.

16. A CIC of claim 1 comprising a reactive linking group.

17. A CIC of claim 16 comprising a reactive thio group.

18. A CIC of claim 1 linked to a polypeptide.

19. The CIC of claim 11 having a structure selected from the group consisting of

5′-TCGTCGA-3′-HEG-5′-ACGTTCG-3′-HEG-5′-AGATGAT-3′

5′-TCGTCG-3′-HEG-5′-ACGTTCG-3′-HEG-5′-AGATGAT-3′

5′-TCGTCGA-3′-HEG-5′-TCGTCGA-3′-HEG-5′-TCGTCGA-3′

5′-TCGTCG-3′-HEG-5′-TCGTCG-3′-HEG-5′-TCGTCG-3′

5′-TCGTCG-3′-HEG-5′-AACGTT-3′-HEG-5′-AGATGAT-3′

5′-TCGTCG-3′-HEG-5′-ACGTTCG-3′-HEG-5′-AGATGAT-3′-TEG

HEG-5′-TCGTCG-3′-HEG-5′-ACGTTCG-3′-HEG-5′-AGATGAT-3′-TEG

5′-TCGTTTT-3′-HEG-5′-TCGTTTT-3′-HEG-5′-TCGTTTT-3′

5′-TCGTCGT-3′-HEG-5′-TCGTCGT-3′-HEG-5′-TCGTCGT-3′

5′-TCGAGAT-3′-HEG-5′-TCGAGAT-3′-HEG-5′-TCGAGAT-3′

5′-TCGTCGT-3′-HEG-5′-TGTCGTT-3′-HEG-5′-TGTCGTT-3′

5′-TCGTCGA-3′-HEG-5′-ACGTTCG-3′-HEG-5′-TCGTCGA-3′

5′-TCGTCGA-3′-HEG-5′-ACGTTCG-3′-HEG-5′-GGGGGG-3′

5′-TCGAACG-3′-HEG-5′-TCGAACG-3′-HEG-5′-TCGAACG-3′

5′-TCGACGT-3′-HEG-5′-TCGACGT-3′-HEG-5′-TCGACGT-3′

5′-TCGTCGA-3′-HEG-5′-AACGTTC-3′-HEG-5′-AGATGAT-3′

5′-TCGTCGA-3′-HEG-5′-AACGTTC-3′-HEG-5′-TCGTCGA-3′

5′-TCGTCGA-3′-HEG-5′-AGATGAT-3′-HEG-5′-ACGTTCG-3′

5′-TCGACTC-3′-HEG-5′-TCGAGCG-3′-HEG-5′-TTCTCTT-3′

5′-TCGTCGA-3′-HEG-5′-TCGTCGA-3′-HEG-3′-AGCTGCT-5′

5′-TCGAT-3′-HEG-5′-TCGAT-3′-HEG-5′-TCGAT-3′-HEG-5′-TCGAT-3′

5′-TCGTCGA-3′-HEG-5′-TCGTCGA-3′-HEG-5′-AACGTTC-3′-HEG-5′-AGAT-3′

5′-TCGACGT-3′-HEG-5′-TCGACGT-3′-HEG-5′-TCGACGT-3′-HEG-5′-TCGACGT-3′

5′-TCGATTT-3′-HEG-5′-TCGATTT-3′-HEG-5′-TCGATTT-3′

5′-TCGCTTT-3′-HEG-5′-TCGCTTT-3′-HEG-5′-TCGCTTT-3′

5′-TCGGTTT-3′-HEG-5′-TCGGTTT-3′-HEG-5′-TCGGTTT-3′.

20. A composition comprising a CIC of claim 19 and a pharmaceutically acceptable excipient.

21. A composition comprising a CIC of claim 19 and further comprising an antigen.

22. A composition comprising a CIC of claim 19 and further comprising a cationic microsphere.

23. The composition of claim 22 wherein the microsphere comprises a polymer of lactic acid and glycolic acid.

24. A CIC of claim 19 further comprising a reactive thio group.

25. A CIC of claim 19 linked to a polypeptide.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded May 14, 2021
From: CRG SERVICING LLC, AS ADMINISTRATIVE AGENT
To: DYNAVAX TECHNOLOGIES CORPORATION
Reel/Frame 056252/0515 →
SECURITY INTEREST Recorded Feb 22, 2018
From: DYNAVAX TECHNOLOGIES CORPORATION
To: CRG SERVICING LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 045441/0469 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2002
From: FEARON, KAREN L.; DINA, DINO; TUCK, STEPHEN F.
To: DYNAVAX TECHNOLOGIES COPRORATION
Reel/Frame 013281/0683 →
Continuity (3)
Provisional Application 6029988300 · Jun 21, 2001
Provisional Application 6037525300 · Apr 23, 2002
Related Publication 20030175731A1 · Sep 18, 2003