IP Library Granted Patent US 9,220,765
Granted Patent B2
US 9,220,765 · App. 14/696,728 · Granted Dec 29, 2015

Bacterial ribonucleic acid cell wall compositions and methods of making and using them

Inventors: Nigel C. Phillips (Pointe-Claire, CA); Danbing Ke (Kirkland, CA); Zdenek Richard Holan (Montreal, CA); Mario C. Filion (Laval, CA); Mohamed Elrafih (Belleville, CA); Iqubal Velji (Montreal, CA)
Assignee: BIONICHE UROLOGY IP INC.
A61K39/04A61K31/7084A61K31/7088A61K31/7105A61K35/74A61K39/39C12N1/06A61K2039/53A61K2039/55555A61K2039/55594
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Quick Facts
Patent No.
US 9,220,765
App. No.
14/696,728
Granted
Dec 29, 2015
Kind
B2
Abstract

The present invention relates to novel bacterial and mycobacterial compositions containing RNA and cell walls, and methods for making and using these compositions. These compositions have immune stimulating and anti-cancer activity.

Claims (61)

1. A composition comprising mycobacterial cell wall fragments and associated mycobacterial RNA,

wherein the the mycobacterial cell wall fragments and the associated mycobacterial RNA are isolated from mycobacterial cells,

wherein the composition does not contain phenol or Streptomyces griseus protease,

and wherein the mycobacterial RNA is in the form of oligoribonucleotides and polyribonucleotides about 2 to about 150 bases in length.

2. The composition of claim 1 , wherein the mycobacterial cells are cells of one or more mycobacteria selected from the group consisting of Mycobacterium phlei, Mycobacterium vaccae, Mycobacterium smegmatis, Mycobacterium avium subspecies paratuberculosis and Mycobacterium bovis BCG.

3. The composition of claim 1 , further comprising intact mycobacterial cells.

4. The composition of claim 3 , wherein the intact mycobacterial cells comprise from about 0.05% to about 95% or about 0.19% to about 19.6% by weight (wt %) of the composition.

5. The composition of claim 3 , wherein the intact mycobacterial cells are intact cells of one or more mycobacteria selected from the group consisting of Mycobacterium phlei, Mycobacterium vaccae, Mycobacterium smegmatis, Mycobacterium avium subspecies paratuberculosis and Mycobacterium bovis BCG.

6. The composition of claim 3 , wherein the intact mycobacterial cells are inactivated mycobacterial cells.

7. The composition of claim 1 , wherein the mycobacterial cells are cells of Mycobacterium phlei.

8. The composition of claim 7 , further comprising intact cells of Mycobacterium phlei.

9. The composition of claim 8 , wherein the intact mycobacterial cells of Mycobacterium phlei comprise from about 0.05% to about 95% or about 0.19% to about 19.6% by weight (wt %) of the composition.

10. The composition of claim 8 , wherein the intact cells of Mycobacterium phlei are inactivated intact cells of Mycobacterium phlei.

11. The composition of claim 1 , wherein the oligoribonucleotides and polyribonucleotides are about 20 to about 40 bases in length, or about 2 to about 40 bases in length.

12. The composition of claim 1 , further comprising a pharmaceutically acceptable carrier or delivery system.

13. A composition comprising isolated mycobacterial RNA associated with mycobacterial cell wall fragments, the composition made by a method comprising sequential steps of:

A) disrupting a mycobacterial cell biomass to generate mycobacterial cell wall fragments, mycobacterial cell wall fragments and associated RNA, disrupted mycobacterial cells, intact mycobacterial cells, and mycobacterial RNA;

B) optionally separating intact mycobacterial cells from the generated mycobacterial cell wall fragments and associated RNA; and,

C) separating the soluble, cytosolic contents of a portion of the disrupted mycobacterial cells from the generated mycobacterial cell wall fragments and associated mycobacterial RNA; and,

after step A, optional step B or after step C, further comprising heating a composition obtained in a previous step at a temperature sufficient to generate oligoribonucleotides and polyribonucleotides of about 2 to about 150 bases in length.

14. The composition of claim 13 , wherein the mycobacterial cell biomass comprises cells of one or more mycobacteria selected from the group consisting of Mycobacterium phlei, Mycobacterium vaccae, Mycobacterium smegmatis, Mycobacterium avium subspecies paratuberculosis and Mycobacterium bovis BCG.

15. The composition of claim 13 , wherein the composition does not contain phenol or Streptomyces griseus protease.

16. The composition of claim 13 , wherein the heating step generates oligoribonucleotides and polyribonucleotides of about 20 to about 40 bases in length, or about 2 to about 40 bases in length.

17. The composition of claim 13 , wherein the mycobacterial cell biomass is a biomass of Mycobacterium phlei cells.

18. The composition of claim 13 , wherein the method further comprises repeating step A and optionally step B to control the number of the intact mycobacterial cells.

19. The composition of claim 13 , wherein the intact mycobacterial cells comprise from about 0.05% to about 95% or about 0.19% to about 19.6% by weight (wt %) of the composition.

20. The composition of claim 13 , wherein the intact mycobacterial cells are inactivated during the heating step.

21. A composition comprising isolated bacterial RNA associated with bacterial cell wall fragments, the composition obtained by a method comprising the sequential steps of:

A) disrupting a bacterial cell biomass to generate bacterial cell wall fragments, bacterial cell wall fragments and associated RNA, disrupted bacterial cells, intact bacterial cells, and bacterial RNA;

B) optionally separating intact bacterial cells from the generated bacterial cell wall fragments and associated RNA; and,

C) separating the soluble, cytosolic contents of a portion of the disrupted bacterial cells from the generated bacterial cell wall fragments and associated RNA; and,

after step A, optional step B or after step C, further comprising heating a composition obtained in a previous step at a temperature sufficient to generate oligoribonucleotides and polyribonucleotides of about 2 to about 150 bases in length.

22. The composition of claim 21 , wherein the isolated bacterial RNA associated with bacterial cell wall fragments are from gram positive bacteria or gram negative bacteria.

23. The composition of claim 21 wherein the intact bacterial cells are inactivated during the step of heating.

24. The composition of claim 21 , wherein the temperature is sufficient to generate oligoribonucleotides and polyribonucleotides of about 2 to about 40 bases in length.

25. The composition of claim 21 , wherein the composition does not contain phenol or Streptomyces griseus protease.

26. A composition comprising bacterial cell wall fragments and associated bacterial RNA,

wherein the the bacterial cell wall fragments and the associated bacterial RNA are isolated from bacterial cells,

wherein the composition does not contain phenol or Streptomyces griseus protease,

and wherein the bacterial RNA is in the form of oligoribonucleotides and polyribonucleotides about 2 to about 150 bases in length.

27. The composition of claim 26 , wherein the bacterial cells are cells of gram positive bacteria or gram negative bacteria.

28. The composition of claim 26 , wherein the composition further comprises intact bacterial cells.

29. The composition of claim 28 , wherein the intact bacterial cells are inactivated intact bacterial cells.

30. The composition of claim 26 , wherein the oligoribonucleotides and polyribonucleotides are about 20 to about 40 bases in length, or about 2 to about 40 bases in length.

31. The composition of claim 26 , further comprising a pharmaceutically acceptable carrier or delivery system.

32. A composition comprising mycobacterial RNA and mycobacterial cell wall fragments,

wherein the mycobacterial RNA and the mycobacterial cell wall fragments are isolated from mycobacterial cells,

wherein the composition does not contain phenol or Streptomyces griseus protease,

wherein the mycobacterial RNA is in the form of oligoribonucleotides and polyribonucleotides about 2 to about 150 bases in length,

and wherein the mycobacterial cells are cells of one or more mycobacteria selected from the group consisting of Mycobacterium phlei, Mycobacterium vaccae, Mycobacterium smegmatis, Mycobacterium avium subspecies paratuberculosis and Mycobacterium bovis BCG.

33. The composition of claim 32 , wherein the mycobacterial RNA is associated with the mycobacterial cell wall fragments.

34. The composition of claim 32 , further comprising intact mycobacterial cells.

35. The composition of claim 34 , wherein the intact mycobacterial cells comprise from about 0.05% to about 95% or about 0.19% to about 19.6% by weight (wt %) of the composition.

36. The composition of claim 34 , wherein the intact mycobacterial cells are intact cells of one or more mycobacteria selected from the group consisting of Mycobacterium phlei, Mycobacterium vaccae, Mycobacterium smegmatis, Mycobacterium avium subspecies paratuberculosis and Mycobacterium bovis BCG.

37. The composition of claim 34 , wherein the intact mycobacterial cells are inactivated mycobacterial cells.

38. The composition of claim 32 , wherein the mycobacterial cells are cells of Mycobacterium phlei.

39. The composition of claim 38 , further comprising intact cells of Mycobacterium phlei.

40. The composition of claim 39 , wherein the intact mycobacterial cells of Mycobacterium phlei comprise from about 0.05% to about 95% or about 0.19% to about 19.6% by weight (wt %) of the composition.

41. The composition of claim 40 , wherein the intact cells of Mycobacterium phlei are inactivated intact cells of Mycobacterium phlei.

42. The composition of claim 32 , wherein the oligoribonucleotides and polyribonucleotides are about 20 to about 40 bases in length, or about 2 to about 40 bases in length.

43. The composition of claim 32 , further comprising a pharmaceutically acceptable carrier or delivery system.

Assignments (4)
CORRECTIVE ASSIGNMENT TO CORRECT THE ADDRESS OF THE ASSIGNEE PREVIOUSLY RECORDED AT REEL: 036986 FRAME: 0343. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Dec 1, 2015
From: BIONICHE UROLOGY IP INC.
To: TELESTA THERAPEUTICS IP INC.
Reel/Frame 037177/0450 →
CHANGE OF NAME Recorded Oct 28, 2015
From: BIONICHE UROLOGY IP INC.
To: TELESTA THERAPEUTICS IP INC.
Reel/Frame 036986/0343 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 2, 2015
From: PHILLIPS, NIGEL C.; KE, DANBING; HOLAN, ZDENEK RICHARD; FILION, MARIO C.; VELJI, IQUBAL; ELRAFIH, MOHAMED
To: BIONICHE LIFE SCIENCES INC.
Reel/Frame 036476/0512 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 2, 2015
From: BIONICHE LIFE SCIENCES INC.
To: BIONICHE UROLOGY IP INC.
Reel/Frame 036476/0559 →
Continuity (4)
Continuation 13701954
Provisional Application 61392498 · Oct 13, 2010
Provisional Application 61393589 · Oct 15, 2010
Related Publication 20150224183A1 · Aug 13, 2015