Production of a probiotic composition
US-2024293479-A1 · Sep 5, 2024 · US
US11446336B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11446336-B2 |
| Application number | US-202117325502-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 20, 2021 |
| Priority date | Dec 12, 2018 |
| Publication date | Sep 20, 2022 |
| Grant date | Sep 20, 2022 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention provides a composition comprising a bacterial strain of the genus Parabacteroides, for use in a method of treating or preventing cancer in a subject; wherein the cancer comprises oncogenic ERK signalling.
Opening claim text (preview).
The invention claimed is: 1. A method of treating cancer in a subject in need thereof, comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a bacterial strain of the species Parabacteroides distasonis , wherein the bacterial strain comprises a 16s rRNA gene sequence having at least 98% sequence identity to the polynucleotide sequence of SEQ ID NO: 9, and wherein the cancer comprises oncogenic ERK signaling, and comprises an oncogenic mutation in, or overexpression of, BRAF, NRAS, ARAF, CRAF, EGFR, GRB2, SOS, HRAS, KRAS, MEK1, MEK2, ERK1 or ERK2. 2. The method of claim 1 , wherein the cancer comprises an oncogenic mutation in BRAF. 3. The method of claim 2 , wherein the oncogenic mutation is at amino acid position 600 in BRAF. 4. The method of claim 2 , wherein the oncogenic mutation is selected from the group consisting of V600E, V600K, V600R, V600D, K601E, G469A, G469V, L597R, K601N, G464V, N581S, L597Q, A598V, G464R, G466A, G469E, and any combinations thereof. 5. The method of claim 1 , wherein the cancer comprises V600E mutation in BRAF. 6. The method of claim 2 , wherein the cancer further comprises overexpression of BRAF. 7. The method of claim 1 , wherein the cancer comprises an oncogenic mutation in NRAS, wherein the oncogenic mutation is Q61R. 8. The method of claim 7 , wherein the cancer further comprises overexpression of NRAS. 9. The method of claim 1 , wherein the cancer comprises an oncogenic mutation in KRAS, wherein the oncogenic mutation is G13D. 10. The method of claim 1 , wherein the cancer comprises colorectal cancer or melanoma. 11. The method of claim 1 , wherein the pharmaceutical composition is formulated for delivery to a gastrointestinal tract of the subject. 12. The method of claim 1 , wherein the therapeutically effective amount comprises from about 1×10 3 to about 1×10 11 colony forming units (CFU). 13. The method of claim 1 , wherein the bacterial strain is the Parabacteroides distasonis strain deposited under accession number NCIMB 42382. 14. The method of claim 1 , wherein the bacterial strain comprises a 16s rRNA gene sequence having at least 99% sequence identity to the polynucleotide sequence of SEQ ID NO: 9. 15. The method of claim 1 , wherein the bacterial strain comprises a 16s rRNA gene sequence of the polynucleotide sequence of SEQ ID NO: 9. 16. The method of claim 1 , wherein the subject is immunocompromised or immunosuppressed. 17. A method of treating cancer in a subject in need thereof, comprising administering to the subject a pharmaceutical composition comprising a therapeutically effective amount of a bacterial strain of the species Parabacteroides distasonis, wherein the bacterial strain comprises a 16s rRNA gene sequence having at least 98% sequence identity to the polynucleotide sequence of SEQ ID NO: 9, and wherein the cancer comprises oncogenic ERK signaling. 18. The method of claim 17 , wherein the cancer is colorectal cancer or melanoma. 19. The method of claim 17 , wherein the bacterial strain comprises a 16s rRNA gene sequence having at least 99% sequence identity to the polynucleotide sequence of SEQ ID NO: 9. 20. The method of claim 17 , wherein the therapeutically effective amount comprises from about 1×10 3 to about 1×10 11 colony forming units (CFU).
Probiotics · CPC title
Organic adjuvants · CPC title
Antineoplastic agents · CPC title
Probiotics (probiotic yeast, e.g. saccharomyces A61K36/06) · CPC title
Bacteria (therapeutic use of a bacterial protein A61K38/00) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.