Administration of kynurenine depleting enzymes for tumor therapy

Patent metadata

Field	Value
Publication number	US-9808486-B2
Application number	US-201414473040-A
Country	US
Kind code	B2
Filing date	Aug 29, 2014
Priority date	Aug 30, 2013
Publication date	Nov 7, 2017
Grant date	Nov 7, 2017

Abstract

Methods and compositions related to the use of a protein with kynureninase activity are described. For example, in certain aspects there may be disclosed a modified kynureninase capable of degrading kynurenine. Furthermore, certain aspects of the invention provide compositions and methods for the treatment of cancer with kynurenine depletion using the disclosed proteins or nucleic acids.

First claim

What is claimed is:

1. A method of treating a subject having a tumor comprising administering to the subject an effective amount of a pharmaceutical formulation comprising:
(i) a kynureninase polypeptide comprising the sequence set forth by SEQ ID NOs: 7, 8, 10-52 or 57; or
(ii) a kynureninase polypeptide comprising a sequence having at least 95% identity to SEQ ID NOs: 7, 8, 10-52 or 57, wherein said polypeptide has kynureninase activity
and a pharmaceutically acceptable carrier.

2. The method of claim 1 , wherein the kynureninase is an isolated, modified human kynureninase enzyme, said modified enzyme having at least one substitution relative to native human kynureninase (see SEQ ID NO: 8), said at least one substitution including a Met or Leu substitution for a Phe normally found at position 306 of native human kynureninase.

3. The method of claim 2 , wherein the at least one substitution comprises Phe306Met.

4. The method of claim 2 , wherein the at least one substitution comprises Phe306Leu.

5. The method of claim 2 , wherein the kynureninase further comprises a heterologous peptide segment.

6. The method of claim 5 , wherein the heterologous peptide segment is an XTEN peptide, an IgG Fc, an albumin, or an albumin binding peptide.

7. The method of claim 1 , wherein the kynureninase is coupled to polyethylene glycol (PEG).

8. The method of claim 7 , wherein the kynureninase is coupled to PEG via one or more Lys or Cys residues.

9. The method of claim 1 , wherein the kynureninase has greater catalytic activity towards kynurenine than 3′-OH kynurenine.

10. The method of claim 1 , wherein the kynureninase is a bacterial kynureninase, wherein the bacterial kynureninase comprises an amino acid sequence at least 95% identical to any of SEQ ID NOs: 7, 13-52, and 57 and has kynureninase activity.

11. The method of claim 1 , wherein the kynureninase is a primate or human kynureninase, wherein the primate kynureninase comprises an amino acid sequence at least 95% identical to any of SEQ ID NOs: 8 and 10-12 and has kynureninase activity.

12. The method of claim 1 , wherein the subject is a human patient.

13. The method of claim 1 , wherein the formulation is administered intratumorally, intravenously, intradermally, intraarterially, intraperitoneally, intralesionally, intracranially, intraarticularly, intraprostaticaly, intrapleurally, intratracheally, intraocularly, intranasally, intravitreally, intravaginally, intrarectally, intramuscularly, subcutaneously, subconjunctival, intravesicularlly, mucosally, intrapericardially, intraumbilically, orally, by inhalation, by injection, by infusion, by continuous infusion, by localized perfusion bathing target cells directly, via a catheter, or via a lavage.

14. The method of claim 1 , further comprising administering at least a second anticancer therapy to the subject.

15. The method of claim 14 , wherein the second anticancer therapy is a surgical therapy, chemotherapy, radiation therapy, cryotherapy, hormone therapy, immunotherapy or cytokine therapy.

16. The method of claim 14 , wherein the second anticancer therapy comprises an anti-PD1, anti-CTLA-4, or anti-PD-L1 antibody.

Assignees

• Univ Texas

Inventors

• Georgiou George
• Stone Everett

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61K38/00

  Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title

• C12Y307/01003

  Kynureninase (3.7.1.3) · CPC title

• A61K38/46

  Hydrolases (3) · CPC title