IP Library Granted Patent US 10,555,976
Granted Patent B2
US 10,555,976 · App. 16/423,375 · Granted Feb 11, 2020

Method of reducing the likelihood of skin cancer in an individual human being

Inventor: Joseph E. Kovarik (Englewood, CO)
A61K35/74A61K31/58A61K31/715A61K38/1709A61K38/1758A61K2035/11
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Quick Facts
Patent No.
US 10,555,976
App. No.
16/423,375
Granted
Feb 11, 2020
Kind
B2
Abstract

Compositions, systems and methods of improving the health of the microbiome of an individual's skin relate to the provision of skin contacting formulations containing beneficial bacteria and other microbe components to foster the growth and maintenance of a healthy skin microbiome.

Claims (20)

1. A method of reducing the likelihood of skin cancer in an individual human being, said method comprising: administering a therapeutically effective amount of a bacterial formulation comprising Nitrosomonas eutropha adapted to produce p53, said bacterial formulation comprising a lotion, ointment or gel adapted to be rubbed onto a region of an individual's skin wherein at least some bacteria in the bacterial formulation have been modified by using a using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Francisella 1(Cpf1) system to remove a virulence factor of the at least some bacteria.

2. The method as set forth in claim 1 , wherein the bacterial formulation further includes Propionibacterium bacteria.

3. The method as set forth in claim 1 , further comprising administering to the skin an extract derived from a helminth selected from the group consisting of Capillaria hepatica, Dicrocoelium dendriticum, Ascaris lumbricoides, Enterobius vermicularis, Trichuris trichiura, Ancylostoma duodenale, Necator americanus, Strongyloides stercoralis, Haemonchus contortus , and Trichinella spiral's.

4. The method as set forth in claim 1 , wherein the bacterial formulation includes at least one arabinogalactan.

5. The method as set forth in claim 1 , wherein the bacterial formulation includes Lactobacillus johnsonii.

6. The method as set forth in claim 1 , wherein the bacterial formulation comprises a topical lotion that comprises at least one of Lactobacillus johnsonii , and Bifidobacterium lognum bacteria.

7. The method as set forth in claim 6 , wherein the topical lotion is administered to an individual's skin as a probiotic bacteriotherapy to treat skin diseases selected from the group consisting of eczema, atopic dermatitis, acne, allergic inflammation, and skin hypersensitivity.

8. The method as set forth in claim 6 , wherein the topical lotion is administered to an individual's skin as a probiotic bacteriotherapy to treat ultra-violet-induced skin damage.

9. The method as set forth in claim 1 , wherein the bacterial formulation comprises proteins produced by said bacterial formulation.

10. The method as set forth in claim 1 , wherein the bacterial formulation enhances protection of skin from harmful ultra-violet radiation.

11. The method as set forth in claim 1 , wherein the bacterial formulation comprises a bifidobacterium strain.

12. A method of reducing the likelihood of skin cancer in an individual human being, said method comprising: administering a therapeutically effective amount of a bacterial formulation comprising Nitrosomonas eutropha adapted to produce p53, said bacterial formulation including a bifidobacterium strain modified by using a using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Francisella 1 (Cpf1) system to remove a virulence factor.

13. The method as set forth in claim 12 , wherein the bacterial formulation further includes Propionibacterium bacteria.

14. A method of reducing the likelihood of skin cancer in an individual human being, said method comprising: administering a therapeutically effective amount of a bacterial formulation comprising Nitrosomonas eutropha adapted to produce p53, said bacterial formulation comprising Propionibacterium bacteria, wherein the Propionibacterium bacteria is modified by using a using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Francisella 1(Cpf1) system to remove a virulence factor.

15. The method as set forth in claim 14 , wherein the bacterial formulation is administered to an individual's skin as a probiotic bacteriotherapy to treat skin diseases selected from the group consisting of eczema, atopic dermatitis, acne, allergic inflammation, and skin hypersensitivity.

16. The method as set forth in claim 14 , further comprising administering to the skin an extract derived from a helminth selected from the group consisting of Capillaria hepatica, Dicrocoelium dendriticum, Ascaris lumbricoides, Enterobius vermicularis, Trichuris trichiura, Ancylostoma duodenale, Necator americanus, Strongyloides stercoralis, Haemonchus contortus , and Trichinella spiralis.

17. The method as set forth in claim 14 , wherein the bacterial formulation comprises a topical lotion that comprises at least one of Lactobacillus johnsonii , and Bifidobacterium lognum bacteria.

18. The method as set forth in claim 14 , wherein the bacterial formulation includes at least one arabinogalactan.

19. A method of reducing the likelihood of skin cancer in an individual human being, said method comprising: administering a therapeutically effective amount of a bacterial formulation comprising Nitrosomonas eutropha adapted to produce p53, said bacterial formulation comprising Propionibacterium bacteria, wherein the Propionibacterium bacteria is modified by using a using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Francisella 1 (Cpf1) system to remove a virulence factor, and administering to the individual human being an immune checkpoint inhibitor.

20. The method as set forth in claim 19 , wherein the immune checkpoint inhibitor is selected from the group consisting of nivolumab, pembrolizumab, pidilizumab, AMP-224, AMP-514, STI-A1110, TSR-042, RG-7446, BMS-936559, MEDI-4736, MSB-0020718C, AUR-012 and STI-A1010.

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 (28)
Continuation 16160336 · Oct 15, 2018
Continuation In Part 15639767 · Jun 30, 2017
Continuation In Part 15437976 · Feb 21, 2017
Continuation 15403823 · Jan 11, 2017
Continuation In Part 15270034 · Sep 20, 2016
Continuation In Part 15228454 · Aug 4, 2016
Continuation In Part 15228454 · Aug 4, 2016
Continuation In Part 14954074 · Nov 30, 2015
Continuation In Part 14752192 · Jun 26, 2015
Continuation In Part 14611458 · Feb 2, 2015
Continuation In Part 14574517 · Dec 18, 2014
Continuation In Part 14502972 · Sep 30, 2014
Continuation In Part 14502097 · Sep 30, 2014
Continuation 14307651 · Jun 18, 2014
Continuation 14307651 · Jun 18, 2014
Continuation In Part 14225503 · Mar 26, 2014
Continuation In Part 14079054 · Nov 13, 2013
Continuation 13425913 · Mar 21, 2012
Continuation 13367052 · Feb 6, 2012
Provisional Application 62296186 · Feb 17, 2016
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 61556023 · Nov 4, 2011
Provisional Application 61467767 · Mar 25, 2011
Provisional Application 61439652 · Feb 4, 2011
Related Publication 20190298781A1 · Oct 3, 2019
Cited By (8)
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