IP Library Granted Patent US 10,864,109
Granted Patent B2
US 10,864,109 · App. 16/776,861 · Granted Dec 15, 2020

Method and system for reducing the likelihood of colorectal cancer in a human being

Inventor: Joseph E. Kovarik (Englewood, CO)
A61F5/566A61K31/733A61K35/74A61P35/00
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Quick Facts
Patent No.
US 10,864,109
App. No.
16/776,861
Granted
Dec 15, 2020
Kind
B2
Abstract

A system and method for reducing the likelihood of colorectal cancer in a human being includes the modification of an individual's gut microbes by employing a Clustered Regularly Interspaced Short Palindromic Repeats-CRISPR-associated system (CRISPR-Cas) or Clustered Regularly Interspaced Short Palindromic Repeats from Prevotella and Francisella 1 (CRISPR/Cpf1) system to modify only bacterial genes of bacteria that reside in the human gut that are non-homologous to those encompassed in the human genome, and in particular, to administer a therapeutically effective amount of a bacterial formulation comprising F. prausnitzii that has been modified to produce one of alliin or butyrate.

Claims (20)

1. A method for reducing the likelihood of colorectal cancer in an individual human being, said method comprising: substantially reducing the human being's resident populations of gut microbes prior to administering a therapeutically effective amount of a bacterial formulation comprising Faecalibacterium prausnitzii ; and providing inulin in an amount sufficient to reduce the pH in the colon of the human being to achieve acidifying of the colon and wherein said bacterial formulation further includes a microbe comprising Veillonella.

2. The method of claim 1 , wherein the Faecalibacterium prausnitzii bacteria employed are isolated from a human being's stool.

3. The method of claim 1 , wherein the Faecalibacterium prausnitzii bacteria employed are from the human being treated.

4. The method of claim 1 , wherein the bacterial formulation comprises bacteria modified via a clustered regularly interspaced short pallindromic repeats (CRISPR) CRISPR associated protein (Cas) system to express p53.

5. The method of claim 1 , further comprising reducing H. pylori populations in the individual human being.

6. The method of claim 1 , wherein the colon is acidified to a degree that intestinal Mg.sup.2+ absorption by the human being is enhanced.

7. The method of claim 1 , wherein the bacterial formulation further comprises a bacterium selected from the group consisting of comprising Chlamydia, Shigella flexneri, Mycoplasma , and H. pylori.

8. The method of claim 1 , wherein the bacterial formulation further comprises Chlamydia bacterium.

9. The method of claim 1 , wherein the bacterial formulation further comprises Shigella flexneri bacterium.

10. The method of claim 1 , wherein the bacterial formulation further comprises Mycoplasma bacterium.

11. The method of claim 1 , wherein the bacterial formulation further comprises H. pylori bacterium.

12. The method of claim 1 , wherein said bacterial formulation further includes a microbe selected from the group consisting of Streptococcus and Treponema.

13. A method for reducing the likelihood of colorectal cancer in an individual human being, said method comprising: substantially reducing the human being's resident populations of gut microbes prior to administering a therapeutically effective amount of a bacterial formulation comprising Faecalibacterium prausnitzii ; and providing inulin in an amount sufficient to reduce the pH in the colon of the human being to achieve acidifying of the colon and wherein said bacterial formulation further includes a microbe comprising Streptococcus.

14. The method of claim 13 , wherein said bacterial formulation further includes a microbe selected from the group consisting of Veillonella and Treponema.

15. The method of claim 13 , wherein the bacterial formulation further comprises a bacterium selected from the group consisting of comprising Chlamydia, Shigella flexneri, Mycoplasma , and H. pylori.

16. The method of claim 13 , wherein the bacterial formulation comprises bacteria modified via a clustered regularly interspaced short pallindromic repeats (CRISPR) CRISPR associated protein (Cas) system to express p53.

17. A method for reducing the likelihood of colorectal cancer in an individual human being, said method comprising: substantially reducing the human being's resident populations of gut microbes prior to administering a therapeutically effective amount of a bacterial formulation comprising Faecalibacterium prausnitzii ; and providing inulin in an amount sufficient to reduce the pH in the colon of the human being to achieve acidifying of the colon, and wherein said bacterial formulation further includes a microbe selected from the group consisting of Prevotella, H. pylori and Treponema , that has been modified by using a CRISPR-Cas or CRISPR-Cpf1 system to excise virulence factor genes.

18. The method of claim 17 , wherein said bacterial formulation further includes a microbe selected from the group consisting of Streptococcus and Veillonella.

19. The method of claim 17 , wherein the bacterial formulation comprises bacteria modified via a clustered regularly interspaced short pallindromic repeats (CRISPR) CRISPR associated protein (Cas) system to express p53.

20. The method of claim 17 , wherein the bacterial formulation further comprises a bacterium selected from the group consisting of comprising Chlamydia, Shigella flexneri, Mycoplasma , and H. pylori.

Assignments (2)
SECURITY INTEREST Recorded Jul 21, 2026
From: SEED HEALTH, INC.
To: JPMORGAN CHASE BANK, N.A., AS LENDER
Reel/Frame 076028/0339 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2022
From: KOVARIK, JOE
To: SEED HEALTH, INC.
Reel/Frame 059690/0210 →
Continuity (24)
Continuation 16142171 · Sep 26, 2018
Continuation In Part 15395419 · Dec 30, 2016
Continuation In Part 14752192 · Jun 26, 2015
Continuation In Part 14225503 · Mar 26, 2014
Continuation 13367052 · Feb 6, 2012
Continuation In Part 15270034 · Sep 20, 2016
Continuation In Part 14954074 · Nov 30, 2015
Continuation In Part 14574517 · Dec 18, 2014
Continuation In Part 15228454 · Aug 4, 2016
Continuation In Part 14611458 · Feb 2, 2015
Continuation In Part 14502097 · Sep 30, 2014
Continuation 14307651 · Jun 18, 2014
Continuation In Part 14079054 · Nov 13, 2013
Continuation 13425913 · Mar 21, 2012
Provisional Application 62274550 · Jan 4, 2016
Provisional Application 61439652 · Feb 4, 2011
Provisional Application 61556023 · Nov 4, 2011
Provisional Application 62072476 · Oct 30, 2014
Provisional Application 62053926 · Sep 23, 2014
Provisional Application 62014855 · Jun 20, 2014
Provisional Application 61919297 · Dec 20, 2013
Provisional Application 62275341 · Jan 6, 2016
Provisional Application 61467767 · Mar 25, 2011
Related Publication 20200163796A1 · May 28, 2020
Cited By (5)
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