Granted Patent B2

US 12,246,043 · App. 18/535,722 · Granted Mar 11, 2025

Inventors: Tye Jensen (Telluride, CO); Joseph E. Kovarik (Englewood, CO); Raja Dhir (Venice, CA)

Assignee: Seed Health, Inc.

A61K35/74A61K31/58A61K31/715A61K35/741A61K35/745A61K35/747A61K38/1709A61K38/1758C12N1/20A61K2035/11A61K2035/115

Abstract

Claims (26)

1. A method of reducing the likelihood of a skin condition comprising acne vulgaris that causes skin inflammation in an individual human being, said method comprising: administering a therapeutically effective amount of a bacterial formulation comprising at least one of a live or a heat-killed bacteria selected from the group consisting of Lactobacillus crispatus , and Cutibacterium acnes , said bacterial formulation comprising a lotion, ointment or gel adapted to be rubbed onto a region of an individual's skin, and

administering to the individual a prebiotic, metabolite, and a postbiotic.

2. The method as set forth in claim 1 , 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 reduce the production of a virulence factor by at least one of said live bacteria in said bacterial formulation.

3. The method as set forth in claim 1 , wherein the live bacteria is Cutibacterium acnes.

4. The method as set forth in claim 3 , further comprising modifying the expression of at least one virulence factor gene selected from the group consisting of virulence factor genes involved in cell adhesion, mediation of inflammation, tissue invasion, and the synthesis of capsule polysaccharides.

5. The method as set forth in claim 3 , further comprising modifying the expression of at least one virulence factor gene selected from the group consisting of virulence factor genes that encode sialidases, neuraminidases, endoglycoceramidases, adhesins, thermal shock proteins, CAMP factors, and lipases.

6. The method as set forth in claim 4 , wherein said virulence factors gene is selected from the group consisting of virulence factor genes that encode adhesin dermatan-sulfate (DsA1 and DsA2), CAMP factors, polyunsaturated fatty acid isomerase, HtaA iron acquisition protein and GehA lipase, and heat shock proteins.

7. The method as set forth in claim 4 , wherein the Cutibacterium acnes is modified to enhance the production by C. acnes to produce short-chain fatty acids selected from the group consisting of propionate, acetate, butyrate and valerate.

8. The method as set forth in claim 7 , wherein the SCFA production by C. acnes suppresses the growth of S. aureus in an amount to reduce the colonization of S. aureus on the skin.

9. The method as set forth in claim 7 , wherein the SCFA production inhibits biofilm formation by S. epidermidis.

10. The method as set forth in claim 3 , wherein the Cutibacterium acnes is modified to produce at least one of: butyrate to achieve beneficial skin conditions; and increased levels of porphyrins in an amount sufficient to positively affect other members of the skin microbiome.

11. The method as set forth in claim 3 , further comprising selectively killing or retarding the growth of a pathogenic bacteria within the individual, said pathogenic bacteria selected from the group consisting of Staphylococcus aureus; Pseudomonas aeruginosa; Klebsiella; Streptococcus; Salmonella; Shigella; Mycobacterium tuberculosis; Enterococcus; E coli; Clostridium; Neisseria gonorrhoeae; Acinetobacter baumannii ; and Campylobacter.

12. The method as set forth in claim 11 , wherein a CRISPR system is employed to perform the selective killing.

13. The method as set forth in claim 12 , wherein said CRISPR Cas system comprises Cas3 and is delivered using a bacteriophage.

14. The method as set forth in claim 11 , wherein said pathogenic bacteria are killed while sparing other commensal bacteria.

15. The method as set forth in claim 1 , further comprising administering at least two probiotic strains to the individual's skin in a concentration of at least 100,000,000 Arbitrary Fluorescence Units (AFU), said at least two probiotic strains being either live or heat-killed and selected from the group consisting of Cutibacterium, Staphylococcus, Corynebacterium, Micrococcus spp., Actinobacteria, Proteobacteria, and Firmicutes.

16. The method as set forth in claim 1 , further comprising administering to the individual's skin at least one probiotic strain that does not upregulate innate immune response genes selected from the group consisting of CXCL1, CXCL3, CXCL8, CXCL10.

17. The method as set forth in claim 1 , further comprising administering to the individual's skin at least one probiotic strain that does not upregulate innate immune response genes selected from the group consisting of IL10RA, PTGS2, F2RL1, TRIM29, TRAF4, LGALS3, CD55, TRIM8, CASP4, IFNGR1, ADA, NOD1, NOS2, and APP.

18. The method as set forth in claim 12 , wherein said pathogenic bacteria are killed while sparing other commensal bacteria, said commensal bacteria selected from the group consisting of C. acnes, Faecalibacterium prausnitzii, Bifidobacterium, Lachnospira, Veillonella, Coprococcus, Akkermansia muciniphila, Nitrosomonas eutropha, Lactobacillus reuteri, Lactobacillus johnsonii, Janthinobacterium , and Rothia.

19. A method of reducing the likelihood of a skin condition comprising acnes vulgaris that causes skin inflammation in an individual human being, said method comprising: administering a therapeutically effective amount of a bacterial formulation comprising at least one of a live or a heat-killed bacteria, wherein said bacterial formulation comprises Lactobacillus crispatus , said bacterial formulation comprising a lotion, ointment or gel adapted to be rubbed onto a region of an individual's skin, and

administering to the individual a prebiotic, metabolite, and a postbiotic.

20. A method of reducing the likelihood of a skin condition comprising acnes vulgaris that causes skin inflammation in an individual human being, said method comprising: administering a therapeutically effective amount of a bacterial formulation comprising at least one of a live or a heat-killed bacteria selected from the group consisting of Lactobacillus crispatus , and Cutibacterium acnes , said bacterial formulation comprising a lotion, ointment or gel adapted to be rubbed onto a region of an individual's skin, and

administering to the individual a prebiotic, metabolite, and a postbiotic;

administering to the individual a cleanser composition comprising at least one of sodium methyl cocoyl taurate, sodium cocoyl glutamate, coco glucoside, caprylyl/capryl glucoside, sodium cocoyl Isethionate, and cetearyl alcohol; a serum composition comprising at least two of the following: indole-3-carbinol, resveratrol, niacinamide, nicotinic acid, nicotinamide mononucleotide, nicotinamide riboside, quercetin, tryptophan, diiodomethane, Boswellia serrata , and indirubin; and at least one barrier-restoring oil comprising at least one of sunflower oil, coconut oil, murumuru oil, sea buckthorn oil, sachi inchi oil, and babbasu oil;

wherein the bacterial formulation produces short-chain fatty acids selected from the group consisting of propionate, acetate, butyrate and valerate; and

administering at least two probiotic strains to the individual's skin in a concentration of at least 100,000,000 Arbitrary Fluorescence Units (AFU), said at least two probiotic strains being either live or heat-killed and selected from the group consisting of Cutibacterium, Staphylococcus, Corynebacterium, Micrococcus spp., Actinobacteria, Proteobacteria, and Firmicutes.

Assignments (2)

Continuity (64)

References Cited (400)