Kynurenine aminotransferase and products thereof for the treatment of arthritic diseases

Patent metadata

Field	Value
Publication number	US-2025367269-A1
Application number	US-202318876683-A
Country	US
Kind code	A1
Filing date	Jun 19, 2023
Priority date	Jun 20, 2022
Publication date	Dec 4, 2025
Grant date	—

Abstract

The present invention relates to the treatment of an arthritic disease such as rheumatoid arthritis with a kynurenine aminotransferase, a living recombinant bacterium which has been genetically modified to express and secrete said kynurenine aminotransferase, and/or a product of said kynurenine aminotransferase which is xanthurenic acid, a derivative thereof, or any pharmaceutically acceptable salt or solvate thereof.

First claim

1 - 17 . (canceled)

18 . A method of treating an arthritic disease comprising administering a composition to a subject in need of treatment, said composition comprising
a kynurenine aminotransferase (KAT), and/or a living recombinant bacterium which has been genetically modified to express and secrete said kynurenine aminotransferase, and/or a product of said kynurenine aminotransferase which is xanthurenic acid, a derivative thereof, or any pharmaceutically acceptable salt or solvate thereof.

19 . The method according to claim 18 , wherein the arthritic disease is selected from the group consisting of rheumatoid arthritis, juvenile idiopathic arthritis, ankylosing spondylitis, cervical spondylosis, gout, psoriatic arthritis, enteropathic arthritis, Lyme disease arthritis, septic arthritis and reactive arthritis.

20 . The method according to claim 19 , wherein the arthritic disease is rheumatoid arthritis.

21 . The method according to claim 18 , wherein the kynurenine aminotransferase is selected from the group consisting of human kynurenine/alpha-aminoadipate aminotransferase (KAT II), human kynurenine-oxoglutarate transaminase 1 (KAT I), human kynurenine-oxoglutarate transaminase 3 (KAT III), human mitochondrial aspartate aminotransferase (KAT IV), orthologs thereof, and variants thereof, said variants having at least 80% sequence identity to human KAT II, human KAT I, human KAT III, human KAT IV or to any ortholog thereof, and exhibiting kynurenine aminotransferase activity.

22 . The method according to claim 21 , wherein the kynurenine aminotransferase is selected from the group consisting of human KAT II, human KAT III, human KAT IV, orthologs thereof, and variants thereof, said variants having at least 80% sequence identity to human KAT II, human KAT III, human KAT IV or to any ortholog thereof, and exhibiting kynurenine aminotransferase activity.

23 . The method according to claim 22 , wherein the kynurenine aminotransferase is selected from the group consisting of human KAT II, orthologs thereof, and variants thereof, said variants having at least 80% sequence identity to human KAT II or to any ortholog thereof, and exhibiting kynurenine aminotransferase activity.

24 . The method according to claim 21 , wherein the kynurenine aminotransferase is selected from the group consisting of KAT proteins of SEQ ID NO: 1 to 32, and variants thereof having at least 80% sequence identity to any sequence of SEQ ID NO: 1 to 32 and exhibiting kynurenine aminotransferase activity.

25 . The method according to claim 21 , wherein the kynurenine aminotransferase is selected from the group consisting of KAT proteins of SEQ ID NO: 10 to 16, and variants thereof having at least 80% sequence identity to any sequence of SEQ ID NO: 10 to 16 and exhibiting kynurenine aminotransferase activity.

26 . The method according to claim 18 , wherein said composition comprises said kynurenine aminotransferase.

27 . The method according to claim 18 , wherein said composition comprises a recombinant bacterium which has been genetically modified to express and secrete said kynurenine aminotransferase.

28 . The method according to claim 27 , wherein said recombinant bacterium is selected from the group consisting of bacteria belonging to the genera Allobaculum, Adlercreutzia, Anaerostipes, Bifidobacterium, Propionibacterium, Bacteroides, Eubacterium, Enterococcus, Ruminococcus and Faecalibacterium, Escherichia coli , and lactic acid bacteria belonging to the genera Lactobacillus, Lactococcus and Streptococcus.

29 . The method according to claim 18 , wherein said composition further comprises nicotinamide adenine dinucleotide or a precursor thereof.

30 . The method according to claim 18 , wherein said composition comprises xanthurenic acid, a derivative thereof or any pharmaceutically acceptable salt or solvate thereof, wherein the xanthurenic acid derivative is of formula (I)

wherein
R 1 , R 2 and R 3 are independently selected from the group consisting of a hydrogen atom, a hydroxyl group, a halogen atom, a —CO—R 8 group or a —CO 2 R 8 group with R 8 being H or a C 1-10 alkyl group, a —NR 9 R 9′ with R 9 and R 9′ being independently a hydrogen atom or a C 1-10 alkyl group, a nitro group, a cyano group, a C 1-10 alkyl, C 2-10 alkenyl or C 2-10 alkynyl group optionally substituted by a halogen atom, and a C 1-10 alkyloxy optionally substituted by a halogen atom;
R 4 and R 6 are independently selected from the group consisting of a hydrogen atom, and a C 1-10 alkyl group; and
R 5 is selected from the group consisting of a hydroxyl group, a hydrogen atom, a —NR 7 R 7′ with R 7 and R 7′ being independently a hydrogen atom or a C 1-10 alkyl group, a C 1-10 alkyl group, and a C 1-10 alkoxy group,
or a tautomeric form thereof.

31 . The method according to claim 30 , wherein the xanthurenic acid derivative is selected from the group consisting of oxo-xanthurenic acid (OXA) and di-oxo-xanthurenic acid (DOXA).

32 . The method according to claim 30 , wherein said composition comprises xanthurenic acid or any pharmaceutically acceptable salt or solvate thereof.

Assignees

• Institut National De Rech Pour Lagriculture Lalimentation Et L’Environnement
• Institut Nat Des Sciences Et Industries Du Vivant Et De Lenvironnement
• Univ Sorbonne
• Hopitaux Paris Assist Publique
• Inst Nat Sante Rech Med
• Centre Nat Rech Scient
• Univ De Lorraine
• Univ Paris Saclay

Inventors

• Sokol Harry
• Moulin David
• Langella Philippe
• Aucouturier Anne
• Bermudez Luis

Classifications

• C12Y206/01063

  Kynurenine--glyoxylate transaminase (2.6.1.63) · CPC title

• C12Y206/01007

  Kynurenine--oxoglutarate transaminase (2.6.1.7) · CPC title

• A61K35/74

  Bacteria (therapeutic use of a bacterial protein A61K38/00) · CPC title

• A61K31/7084

  Compounds having two nucleosides or nucleotides, e.g. nicotinamide-adenine dinucleotide, flavine-adenine dinucleotide · CPC title

• A61K31/47

  Quinolines; Isoquinolines · CPC title