Recombinant modified vaccinia virus ankara (MVA) respiratory syncytial virus (RSV) vaccine

Patent metadata

Field	Value
Publication number	US-10532094-B2
Application number	US-201816185125-A
Country	US
Kind code	B2
Filing date	Nov 9, 2018
Priority date	Aug 1, 2012
Publication date	Jan 14, 2020
Grant date	Jan 14, 2020

Abstract

Provided herein are recombinant modified vaccinia virus Ankara (MVA) strains as improved vaccines against infection with Respiratory Syncytial Virus (RSV virus) and to related products, methods and uses. Specifically, provided herein are genetically engineered recombinant MVA vectors comprising at least one nucleotide sequence encoding an antigenic determinant of an RSV membrane glycoprotein and at least one nucleotide sequence encoding an antigenic determinant of an RSV nucleocapsid protein. Also provided herein are products, methods and uses thereof, e.g., suitable to affect an immune response in a subject, or suitable to diagnose an RSV infection, as well as to determine whether a subject is at risk of recurrent RSV infection.

First claim

The invention claimed is:

1. A method for treating or preventing an RSV in a subject, comprising administering to the subject in a single dose a recombinant modified vaccinia virus Ankara (MVA) comprising at least one nucleotide sequence encoding an antigenic determinant of a respiratory syncytial virus (RSV) membrane glycoprotein F comprising a nucleotide sequence encoding SEQ ID NO:6.

2. The method of claim 1 , wherein the recombinant MVA further comprises at least one nucleotide sequence encoding an RSV nucleocapsid antigenic determinant M2 matrix protein.

3. The method of claim 2 , wherein the recombinant MVA further comprises a nucleotide sequence encoding an antigenic determinant of an RSV N nucleocapsid protein.

4. The method of claim 3 , wherein both the antigenic determinant of the RSV N nucleocapsid and of the RSV M2 matrix protein are encoded by a single open reading frame separated by a self-cleavage protease domain.

5. The method of claim 4 , wherein the self-cleaving protease domain is the protease 2A fragment sequence derived from Foot and Mouth Disease Virus.

6. The method of claim 5 , wherein the single open reading frame comprises a nucleotide sequence encoding the amino acid sequence of SEQ ID NO:18.

7. The method of claim 6 , wherein the single open reading frame comprises the nucleotide sequence of SEQ ID NO:17.

8. The method of claim 1 , wherein the recombinant MVA further comprises at least one nucleotide sequence encoding an antigenic determinant of an RSV G membrane glycoprotein.

9. The method of claim 8 , wherein the nucleotide sequence encoding an antigenic determinant of the RSV G membrane glycoprotein is from an RSV strain A, strain A2, or strain B.

10. The method of claim 9 , wherein the nucleotide sequence encoding an antigenic determinant of the RSV G membrane glycoprotein comprises a nucleotide sequence encoding the amino acid selected from SEQ ID NO:2 and SED ID NO: 8.

11. The method of claim 1 , wherein the MVA is administered in a concentration of 10 4 to 10 9 TCID 50 /ml, 10 5 to 5×10 8 TCID 50 /ml, 10 6 to 10 8 TCID 50 /ml, or 10 7 to 10 8 TCID 50 /ml.

12. The method of claim 1 , wherein the MVA is administered in a dosage of 10 6 to 10 9 TCID 50 , 10 6 to 5×10 8 TCID 50 , 10 7 to 10 8 TCID 50 , 1×10 8 TCID 50 , or 5×10 8 TCID 50 .

13. The method of claim 1 , wherein the MVA is administered in a dosage of 1×10 8 TCID 50 .

14. The method of claim 1 , wherein the MVA is administered in a dosage of 5×10 8 TCID 50 .

15. The method of claim 11 , wherein the MVA is administered in 500 μl.

16. The method of claim 12 , wherein the MVA is administered in 500 μl.

17. The method of claim 13 , wherein the MVA is administered in 500 μl.

Assignees

• Bavarian Nordic As

Inventors

• Cheminay Cédric
• Steigerwald Robin
• Chaplin Paul

Classifications

• A61K2039/572

  cytotoxic response · CPC title

• A61P31/14

  for RNA viruses · CPC title

• A61K2039/545

  characterised by the dose, timing or administration schedule · CPC title

• A61K2039/5256

  expressing foreign proteins · CPC title

• C12N2760/18571

  Demonstrated in vivo effect · CPC title