IP Library Granted Patent US 9,808,519
Granted Patent B2
US 9,808,519 · App. 15/590,257 · Granted Nov 7, 2017

Composition for inducing proliferation or accumulation of regulatory T cells

Inventors: Kenya Honda (Tokyo, JP); Koji Atarashi (Tokyo, JP); Kikuji Itoh (Tokyo, JP); Takeshi Tanoue (Tokyo, JP)
Assignee: The University of Tokyo
A61K39/08A61K2039/52A61K2039/542A61K2039/57
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Quick Facts
Patent No.
US 9,808,519
App. No.
15/590,257
Granted
Nov 7, 2017
Kind
B2
Abstract

It was found that bacteria belonging to the genus Clostridium induce accumulation of regulatory T cells (Treg cells) in the colon. Moreover, the present inventors found that regulatory T cells (Treg cells) induced by from these bacteria suppressed proliferation of effector T-cells. From these findings, the present inventors found that the use of bacteria belonging to the genus Clostridium or a physiologically active substance derived therefrom made it possible to induce proliferation or accumulation of regulatory T cells (Treg cells), and further to suppress immune functions.

Claims (28)

1. A pharmaceutical composition comprising a spore-forming fraction of human fecal matter formulated for delivery to the intestine, wherein the composition induces proliferation and/or accumulation of regulatory T cells, wherein the spore-forming fraction is resistant to chloroform, and wherein the composition is formulated for oral administration.

2. The pharmaceutical composition of claim 1 , wherein the spore-forming fraction is obtained by chloroform treatment of human fecal matter.

3. The pharmaceutical composition of claim 2 , wherein the chloroform treatment includes an incubation step with chloroform of about 1 hour.

4. The pharmaceutical composition of claim 3 , wherein the chloroform treatment includes a step of removal of chloroform with nitrogen gas.

5. The pharmaceutical composition of claim 1 , wherein the composition further comprises a pharmacologically acceptable carrier.

6. The pharmaceutical composition of claim 1 , wherein the composition is in the form of a capsule.

7. The pharmaceutical composition of claim 1 , wherein the composition is formulated for delivery to the colon.

8. The pharmaceutical composition of claim 1 , wherein the composition further comprises a pH sensitive composition comprising one or more enteric polymers.

9. A pharmaceutical composition comprising a spore-forming fraction of human fecal matter formulated for delivery to the intestine, wherein the composition induces proliferation and/or accumulation of regulatory T cells, wherein the spore-forming fraction is resistant to heat, and wherein the composition is formulated for oral administration.

10. The pharmaceutical composition of claim 9 , wherein the spore-forming fraction is obtained by chloroform treatment of human fecal matter.

11. The pharmaceutical composition of claim 10 , wherein the chloroform treatment includes an incubation step with chloroform of about 1 hour.

12. The pharmaceutical composition of claim 11 , wherein the chloroform treatment includes a step of removal of chloroform with nitrogen gas.

13. The pharmaceutical composition of claim 9 , wherein the composition further comprises a pharmacologically acceptable carrier.

14. The pharmaceutical composition of claim 9 , wherein the composition is in the form of a capsule.

15. The pharmaceutical composition of claim 9 , wherein the composition is formulated for delivery to the colon.

16. The pharmaceutical composition of claim 9 , wherein the composition further comprises a pH sensitive composition comprising one or more enteric polymers.

17. A pharmaceutical composition comprising an active ingredient, wherein the active ingredient consists of a spore-forming fraction of human fecal matter, wherein the composition is formulated for delivery to the intestine, wherein the composition induces proliferation and/or accumulation of regulatory T cells, and wherein the composition is formulated for oral administration.

18. The pharmaceutical composition of claim 17 , wherein the spore-forming fraction is resistant to chloroform.

19. The pharmaceutical composition of claim 18 , wherein the spore-forming fraction is obtained by chloroform treatment of human fecal matter.

20. The pharmaceutical composition of claim 19 , wherein the chloroform treatment includes an incubation step with chloroform of about 1 hour.

21. The pharmaceutical composition of claim 20 , wherein the chloroform treatment includes a step of removal of chloroform with nitrogen gas.

22. The pharmaceutical composition of claim 17 , wherein the spore-forming fraction is resistant to heat.

23. The pharmaceutical composition of claim 17 , wherein the composition further comprises a pharmacologically acceptable carrier.

24. The pharmaceutical composition of claim 17 , wherein the composition is in the form of a capsule.

25. The pharmaceutical composition of claim 17 , wherein the composition is formulated for delivery to the colon.

26. The pharmaceutical composition of claim 17 , wherein the composition further comprises a pH sensitive composition comprising one or more enteric polymers.

27. The pharmaceutical composition of claim 1 , wherein the composition does not include Bacteroides.

28. The pharmaceutical composition of claim 9 , wherein the composition does not include Bacteroides.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 7, 2017
From: HONDA, KENYA; ATARASHI, KOJI; TANOUE, TAKESHI; ITOH, KIKUJI
To: THE UNIVERSITY OF TOKYO
Reel/Frame 042930/0694 →
Priority Claims (2)
JP 2010-129134 · Jun 4, 2010 · national
WO PCT/JP2010/071746 · Dec 3, 2010 · international
Continuity (4)
Continuation 15216015 · Jul 21, 2016
Continuation 14492850 · Sep 22, 2014
Continuation 13701467
Related Publication 20170246283A1 · Aug 31, 2017