Use of metalloproteinase inhibitors against bacterial infections

Patent metadata

Field	Value
Publication number	US-10279017-B2
Application number	US-201515322838-A
Country	US
Kind code	B2
Filing date	Jul 3, 2015
Priority date	Jul 3, 2014
Publication date	May 7, 2019
Grant date	May 7, 2019

Abstract

A composition comprising as components a polypeptide IMPIα (including wild type) and/or a polypeptide IMPIα-fusion and at least one antibiotic compound, in particular an aminoglycoside antibiotic, and/or at least one bactericidal compound, wherein the polypeptides, the at least one antibiotic and the at least one bactericidal compound is present in the composition in concentrations which exhibit in combination a synergistic effect against resistant bacteria.

First claim

What is claimed is:

1. A composition comprising: a polypeptide comprising at least 80% sequence identity to SEQ ID NO. 2, wherein the polypeptide is selected from the group consisting of IMPIα, an IMPIα-fusion, and both an IMPIα and an IMPIα-fusion; and at least one antibiotic compound, wherein the at least one antibiotic compound comprises an aminoglycoside antibiotic, further wherein the polypeptide and the at least one antibiotic compound are in concentrations which exhibit in combination a synergistic effect against resistant bacteria.

2. The composition of claim 1 , wherein the polypeptide is selected from the group consisting of SEQ ID NOs: 10, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, and IMPIα-fusions, having amino acid sequences selected from the group consisting of SEQ ID NOs: 6, 8, 12, 86, 88, 90, and 92.

3. A composition of claim 1 , wherein the IMPIα polypeptide has at least 90% sequence identity to SEQ ID No: 2, representing the wild-type of the protein insect metalloproteinase inhibitor IMPIα.

4. A method of treating or preventing a bacterial infection in a subject, the method comprising administering the composition of claim 1 to a subject suffering from or at risk of suffering from a bacterial infection.

5. The method of claim 4 , wherein the at least one antibiotic compound:
(i) is administered in doses lower than inhibitory upon solitary application, or in higher doses up to maximally tolerable doses, and
(ii) is administered essentially simultaneous with IMPIα or separately in an individual dosing scheme, frequency, and treatment duration.

6. A pharmaceutical composition comprising the composition of claim 1 , and a carrier suitable for injection, inhalation or topical application.

7. A method of sterilizing a device comprising coating the device with the composition of claim 1 .

8. The method of claim 7 , wherein the device is an implant.

9. The composition of claim 1 , wherein the polypeptide is SEQ ID NO. 2.

10. The composition of claim 1 , wherein the IMPIα concentration is at 20 μM.

11. The composition of claim 1 , wherein the IMPIα concentration is at 45 μM.

12. The composition of claim 1 , wherein the polypeptide is the IMPIα-fusion.

13. The composition of claim 1 , further comprising a bactericidal compound.

Assignees

• Fraunhofer Ges Zur Foederung Der Angewand Forschung E V
• Fraunhofer Ges Forschung

Inventors

• Salzig Mark
• Vilcinskas Andreas
• Fischer Rainer

Classifications

• A61P43/00

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

• A61P31/04

  Antibacterial agents · CPC title

• A61P31/00

  Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics · CPC title

• A61L2103/05

  Living organisms or biological materials · CPC title

• A61K45/06

  Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title