Human toll-like receptor inhibitors and methods of use thereof

Patent metadata

Field	Value
Publication number	US-9228184-B2
Application number	US-201313842861-A
Country	US
Kind code	B2
Filing date	Mar 15, 2013
Priority date	Sep 29, 2012
Publication date	Jan 5, 2016
Grant date	Jan 5, 2016

Abstract

Provided herein are human Toll-like receptor (TLR)-inhibitors and methods for use in individuals having an autoimmune disease or an inflammatory disorder. The TLR inhibitors of the present disclosure are polynucleotides comprising an inhibitory motif for one or more of TLR7, TLR8 and TLR9.

First claim

We claim:

1. A polynucleotide consisting of the nucleotide sequence of the formula 5′-Q z TIC-N x X 1 X 2 X 3 X 4 X 5 X 6 -M y -3, wherein each of Q, N, X 1 , X 2 , X 3 , X 4 , and M is a nucleotide or nucleotide analog, x is an integer from 0 to 50, y is 0, z is 0, X 5 is G or I, and X 6 is I or A, upper case letters denote DNA, and wherein the polynucleotide does not comprise a CG dinucleotide.

2. A pharmaceutical composition comprising the polynucleotide of claim 1 and a pharmaceutically acceptable excipient.

3. A method of inhibiting a TLR7-dependent and a TLR8-dependent immune response in an individual, the method comprising: administering to the individual the pharmaceutical composition of claim 2 in an amount effective to inhibit the TLR7-dependent and the TLR8-dependent immune response in the individual.

4. A method of inhibiting an immune response in an individual, the method comprising: administering to the individual a pharmaceutical composition in an amount effective to inhibit the immune response in the individual, wherein the pharmaceutical composition comprises a pharmaceutically acceptable excipient and a polynucleotide consisting of the nucleotide sequence of the formula:
5′-Q z TIC-N x X 1 X 2 X 3 X 4 X 5 X 6 -M y -3, wherein each of Q, N, X 1 , X 2 , X 3 , X 4 , and M is a nucleotide or nucleotide analog, x is an integer from 0 to 50, y is 0, z is 0, X 5 is G or I, and X 6 is I or A, upper case letters denote DNA, and wherein the polynucleotide does not comprise a CG dinucleotide.

5. The method of claim 4 , wherein the immune response is associated with an autoimmune disease.

6. The method of claim 5 , wherein inhibiting the immune response ameliorates one or more symptoms of the autoimmune disease.

7. The method of claim 5 , wherein the autoimmune disease is selected from the group consisting of rheumatoid arthritis, pancreatitis, mixed tissue connective disease, systemic lupus erythematosus, antiphospholipid syndrome, irritable bowel disease, type I diabetes mellitus, and Sjogren's disease.

8. The method of claim 5 , wherein the autoimmune disease is Sjogren's disease.

9. The method of claim 5 , wherein the autoimmune disease is associated with RNA-containing immune complexes.

10. The polynucleotide of claim 1 , wherein the polynucleotide is not an antisense sequence or an RNAi molecule.

11. The polynucleotide of claim 1 , wherein the polynucleotide does not comprise 5′-GGGG 3′.

12. The polynucleotide of claim 1 , wherein 5′-GGGG-3′ is present within 5′-N x X 1 X 2 X 3 X 4 -3′ of the formula 5′-Q z TIC-N x X 1 X 2 X 3 X 4 X 5 X 6 -M y -3.

13. The polynucleotide of claim 1 , wherein X 5 is G.

14. The polynucleotide of claim 1 , wherein X 5 is I.

15. The polynucleotide of claim 1 , wherein X 6 is I.

16. The polynucleotide of claim 1 , wherein X 6 is A.

17. The polynucleotide of claim 1 , wherein X 5 X 6 is GI.

18. The polynucleotide of claim 1 , wherein X 5 X 6 is GA.

19. The polynucleotide of claim 1 , wherein X 5 X 6 is II.

20. The polynucleotide of claim 1 , wherein X 5 X 6 is IA.

21. The polynucleotide of claim 1 , wherein the polynucleotide consists of one of the group consisting of SEQ ID NO:36, SEQ ID NO:44, SEQ ID NO:48, SEQ ID NO:56, SEQ ID NO:59, SEQ ID NO:60, SEQ ID NO:61, SEQ ID NO:62, SEQ ID NO:63, SEQ ID NO:64, SEQ ID NO:65, SEQ ID NO:66, SEQ ID NO:67, SEQ ID NO:85, SEQ ID NO:86, SEQ ID NO:87, SEQ ID NO:88, SEQ ID NO:90, SEQ ID NO:91, SEQ ID NO:95, SEQ ID NO:99, SEQ ID NO:103, SEQ ID NO:104, SEQ ID NO:108, SEQ ID NO:109, SEQ ID NO:110, SEQ ID NO:111, SEQ ID NO:114, and SEQ ID NO:115.

22. The polynucleotide of claim 19 , wherein the polynucleotide consists of one of the group consisting of SEQ ID NO:44, SEQ ID NO:60, SEQ ID NO:61, SEQ ID NO:62, SEQ ID NO:63, SEQ ID NO:64, SEQ ID NO:65, SEQ ID NO:66, SEQ ID NO:67, SEQ ID NO:85, SEQ ID NO:86, SEQ ID NO:87, SEQ ID NO:88, SEQ ID NO:90, SEQ ID NO:91, SEQ ID NO:95, SEQ ID NO:103, SEQ ID NO:104, SEQ ID NO:108, SEQ ID NO:109, SEQ ID NO:110, SEQ ID NO:111, SEQ ID NO:114, and SEQ ID NO:115.

23. The polynucleotide of claim 1 , wherein the polynucleotide is less than 40 bases or base pairs in length.

24. The polynucleotide of claim 1 , wherein the polynucleotide is less than 30 bases or base pairs in length.

25. The polynucleotide of claim 1 , wherein at least one internucleotide linkage of the formula 5′-Q x TIC-N x X 1 X 2 X 3 X 4 X 5 X 6 -M x -3 is a phosphate-modified linkage.

26. The polynucleotide of claim 1 , wherein all internucleotide linkages of the formula 5′-Q x TIC-N x X 1 X 2 X 3 X 4 X 5 X 6 -M x -3 are phosphorothioate linkages.

27. The polynucleotide of claim 1 , wherein the polynucleotide does not comprise 5′-GIGG-3′.

28. The polynucleotide of claim 1 , wherein 5′-GIGG-3′ is present within 5′-N x X 1 X 2 X 3 X 4 -3′ of the formula 5′-Q x TIC-N x X 1 X 2 X 3 X 4 X 5 X 6 -M y -3.

Assignees

• Dynavax Tech Corp

Inventors

• Guiducci Cristiana
• Fearon Karen L
• Barrat Franck

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P37/06

  Immunosuppressants, e.g. drugs for graft rejection · CPC title

• A61P3/10

  for hyperglycaemia, e.g. antidiabetics · CPC title

• A61P37/00

  Drugs for immunological or allergic disorders · CPC title

• A61P29/00

  Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title