Mutant fragments of OspA and methods and uses relating thereto

Patent metadata

Field	Value
Publication number	US-9926343-B2
Application number	US-201615267372-A
Country	US
Kind code	B2
Filing date	Sep 16, 2016
Priority date	Jul 6, 2012
Publication date	Mar 27, 2018
Grant date	Mar 27, 2018

Abstract

The present invention relates to a polypeptide comprising a mutant fragment of an outer surface protein A (OspA), a nucleic acid coding the same, a pharmaceutical composition (particularly for use as a medicament of in a method of treating or preventing a Borrelia infection) comprising the polypeptide and/or the nucleic acid, a method of treating or preventing a Borrelia infection and a method of immunizing a subject.

First claim

What is claimed is:

1. A method for producing a polypeptide comprising a fragment of an outer surface protein A (OspA), wherein the OspA fragment is defined by SEQ ID NO: 216, the method comprising the following steps:
a) introducing a vector encoding the polypeptide into a host cell,
b) growing the host cell under conditions allowing for expression of said polypeptide,
c) homogenizing said host cell, and
d) subjecting the host cell homogenate to purification steps.

2. The method according to claim 1 , wherein the polypeptide comprises a heterodimer selected from the group consisting of Lip-S1D1-S2D1(SEQ ID NO: 186), Lip-S2D1-S1D1 (SEQ ID NO: 192), Lip-S1D1-S2D4 (SEQ ID NO: 198) and Lip-S2D4-S1D1 (SEQ ID NO: 203).

3. The method according to claim 1 , wherein the polypeptide consists of a heterodimer selected from the group consisting of Lip-S1D1-S2D1 (SEQ ID NO: 186), Lip-S2D1-S1D1 (SEQ ID NO: 192), Lip-S1D1-S2D4 (SEQ ID NO: 198) and Lip-S2D4-S1D1 (SEQ ID NO: 203).

4. The method according to claim 1 , wherein the vector comprises a nucleic acid molecule encoding said polypeptide.

5. The method according to claim 4 , wherein said nucleic acid molecule encoding said polypeptide is defined by SEQ ID NO: 48.

6. The method according to claim 1 , wherein said vector is pET28b(+).

7. The method according to claim 1 , wherein said host cell is E. coli.

8. The method according to claim 7 , wherein said E. coli is an E. coli BL21 cell.

9. The method according to claim 1 , wherein said purification steps comprise enriching the polypeptide in a lipid phase separation and purifying over a gel filtration column.

10. The method according to claim 9 , wherein said purification steps further comprise processing over a buffer exchange column.

11. A method for producing a pharmaceutical composition comprising a polypeptide comprising a fragment of an outer surface protein A (OspA), wherein the OspA fragment is defined by SEQ ID NO: 216, the method comprising combining said polypeptide with one or more pharmaceutically acceptable carriers or excipients.

12. The method according to claim 11 , wherein said polypeptide comprises a heterodimer selected from the group consisting of Lip-S1D1-S2D1(SEQ ID NO: 186), Lip-S2D1-S1D1(SEQ ID NO: 192), Lip-S1D1-S2D4 (SEQ ID NO: 198) and Lip-S2D4-S1D1(SEQ ID NO: 203).

13. The method according to claim 11 , wherein said polypeptide consists of a heterodimer selected from the group consisting of Lip-S1D1-S2D1 (SEQ ID NO: 186), Lip-S2D1-S1D1 (SEQ ID NO: 192), Lip-S1D1-S2D4(SEQ ID NO: 198) and Lip-S2D4-S1D1 (SEQ ID NO: 203).

14. The method according to claim 11 , wherein said pharmaceutical composition comprises Lip-S1D1-S2D1 (SEQ ID NO: 186) and Lip-S5D1-S6D1 (SEQ ID NO: 190).

15. The method according to claim 11 , wherein said one or more pharmaceutically acceptable carriers or excipients are selected from the group consisting of saline, buffered saline, dextrose, water, glycerol, ethanol and adjuvants.

16. The method according to claim 15 , wherein said buffered saline is phosphate buffered saline.

17. The method according to claim 15 , wherein said adjuvant is aluminium hydroxide.

18. The method according to claim 11 , wherein said pharmaceutical composition is a vaccine.

Assignees

• Valneva Austria Gmbh

Inventors

• Comstedt Pär
• Hanner Markus
• Lundberg Urban
• Meinke Andreas
• Schüler Wolfgang
• Wizel Benjamin

Classifications

• A61P31/10

  Antimycotics · CPC title

• A61P31/04

  Antibacterial agents · CPC title

• A61P31/12

  Antivirals · CPC title

• A61K39/02

  Bacterial antigens · CPC title

• C07K14/20 Primary

  from Spirochaetales (O), e.g. Treponema, Leptospira · CPC title