IP Library › Granted Patent US 12,246,046
Granted Patent B2
US 12,246,046 · App. 18/463,461 · Granted Mar 11, 2025

Compositions and methods for the treatment of type 1 diabetes

Inventors: Pieter Rottiers (De Pinte, BE); Lothar Steidler (Lokeren, BE)
Assignee: INTREXON ACTOBIOTICS N.V.
A61K35/747A61K35/744A61K35/745A61K39/3955A61K2039/523
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Quick Facts
Patent No.
US 12,246,046
App. No.
18/463,461
Granted
Mar 11, 2025
Kind
B2
Abstract

Provided herein are compositions and methods for the treatment of type 1 diabetes (T1D) in mammalian subjects. The compositions include lactic acid fermenting bacteria (LAB) expressing an IL-2 gene and a T1D-specific self-antigen (e.g., proinsulin (PINS)) gene. Exemplary methods include: orally administering to a mammalian subject, a therapeutically effective amount of the composition. The composition can be administered to the subject mucosally, resulting in delivery of the LAB into the gastrointestinal tract, where the LAB is released. Bioactive polypeptides expressed by the LAB are thus administered via mucosal delivery. The LAB may be selected to deliver a low-dose of IL-2 to the subject. The methods may not require concomitant systemic anti-CD3 antibody treatment. The methods may be suited for subjects possessing residual beta-cell function, e.g., those with recent-onset T1D.

Claims (21)

1. A genetically modified Lactococcus lactis bacterium comprising an exogenous nucleic acid encoding human interleukin-2 (hIL-2) polypeptide and an exogenous nucleic acid encoding human proinsulin (hPINS) polypeptide, both of which are integrated into the chromosome of the genetically modified L. lactis bacterium,

wherein said nucleic acid encoding said hPINS polypeptide comprises a polycistronic expression unit comprising, in 5′ to 3′ order, glyceraldehyde 3-phosphate dehydrogenase gene (gapB) with its promoter, and usp45 secretion leader (SSusp45) transcriptionally and translationally coupled to the sequence encoding said hPINS polypeptide;

wherein said nucleic acid encoding said hIL-2 polypeptide comprises a polycistronic expression unit comprising, in 5′ to 3′ order, phosphopyruvate hydratase gene (eno) with its promoter, and usp45 secretion leader (SSusp45) transcriptionally and translationally coupled to the sequence encoding said hIL-2 polypeptide; and

wherein the genetically modified L. lactis bacterium further comprises the following genetic modifications:

(a) inactivation of thyA;

(b) inactivation of trePP;

(c) inactivation of ptcC;

(d) addition of an exogenous otsB; and

(e) expression of pts/and pts//under the control of a constitutive promoter.

2. The genetically modified L. lactis bacterium of claim 1 , wherein said hPINS polypeptide comprises an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 6, and wherein said hIL-2 polypeptide comprises an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 3.

3. The genetically modified L. lactis bacterium of claim 1 , wherein said nucleic acid encoding hPINS polypeptide comprises SEQ ID NO: 57.

4. The genetically modified L. lactis bacterium of claim 1 , wherein said nucleic acid encoding said hIL-2 polypeptide comprises SEQ ID NO: 46.

5. A composition comprising the genetically modified L. lactis bacterium of claim 1 , and a pharmaceutically acceptable carrier.

6. A method of treating type 1 diabetes mellitus (T1D) in a mammalian subject in need thereof comprising orally administering to the mammalian subject a therapeutically effective amount of the genetically modified L. lactis bacterium of claim 1 .

7. The method of claim 6 , wherein the genetically modified L. lactis bacterium delivers said hIL-2 polypeptide and said hPINS polypeptide to the mucosa of said mammalian subject.

8. The method of claim 6 , wherein no anti-CD3 antibody is further administered to said mammalian subject.

9. The method of claim 6 , further comprising administering an anti-CD3 antibody to said mammalian subject.

10. The method of claim 9 , wherein said anti-CD3 antibody is administered simultaneously with said composition to said mammalian subject.

11. The method of claim 6 , wherein said mammalian subject has been diagnosed with TID within the previous 12 months prior to administering the genetically modified L. lactis bacterium.

12. The method of claim 6 , wherein said mammalian subject is a human patient having a fasting blood C-peptide concentration between about 0.2 and about 1.0 nmol/L; or has a stimulated blood C-peptide concentration between about 0.5 and about 4.0 nmol/L.

13. The method of claim 6 , wherein the genetically modified L. lactis bacterium is administered in a unit dosage form comprising from about 1×10 4 to about 1×10 12 colony-forming units (cfu); about 1×10 6 to about 1×10 12 cfu; or about 1×10 9 to about 1×10 12 cfu.

Continuity (5)
Continuation 17150352 · Jan 15, 2021
Division 16069947
Provisional Application 62278493 · Jan 14, 2016
Provisional Application 62350472 · Jun 15, 2016
Related Publication 20240082323A1 · Mar 14, 2024
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