US2021196814A1PendingUtilityA1

Recombinant Modified Vaccinia Virus Ankara (MVA) Respiratory Syncytial Virus (RSV) Vaccine

Assignee: BAVARIAN NORDIC ASPriority: Aug 1, 2012Filed: Mar 15, 2021Published: Jul 1, 2021
Est. expiryAug 1, 2032(~6 yrs left)· nominal 20-yr term from priority
C12Q 1/70C12Q 1/6851C12N 2760/18522C12N 2710/24143C12N 2710/24121C12N 15/86C12N 7/00C07K 14/005A61K 2039/543A61K 39/155C12N 2760/18534C12N 15/863A61P 31/14A61P 31/12A61K 2039/57A61K 39/285A61K 39/275A61K 39/12A61K 2039/545A61K 2039/572C07K 2319/00C12N 2760/18571A61K 2039/5254A61K 2039/5256C12N 2710/24171A61K 2039/575C12N 2710/24142C07K 14/07C12N 15/09
74
PatentIndex Score
0
Cited by
0
References
0
Claims

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

Claims

exact text as granted — not AI-modified
We claim: 
     
         1 . A method of decreasing RSV load in the lungs of a subject comprising administering to the subject a recombinant modified vaccinia virus Ankara (MVA) comprising a nucleotide sequence encoding at least one antigenic determinant of a respiratory syncytial virus (RSV) membrane glycoprotein to the subject, wherein when the subject is exposed to RSV, the load of RSV in the lungs is decreased. 
     
     
         2 . The method of  claim 1 , wherein said recombinant modified vaccinia virus Ankara (MVA) comprises
 (a) at least one nucleotide sequence encoding an antigenic determinant of a respiratory syncytial virus (RSV) membrane glycoprotein, wherein the nucleotide sequence encodes an RSV F antigenic determinant;   (b) at least one nucleotide sequence comprising an open reading frame that encodes an RSV nucleocapsid antigenic determinant that is an RSV N nucleocapsid protein and an RSV nucleocapsid antigenic determinant that is an RSV M2 matrix protein; and further comprising:   (c) at least one nucleotide sequence encoding an antigenic determinant of an RSV G membrane glycoprotein.   
     
     
         3 . The method of  claim 1 , wherein the nucleotide sequence in (a) encodes a full-length RSV F membrane glycoprotein. 
     
     
         4 . The method of  claim 1 , wherein the nucleotide in (a) is from RSV strain A. 
     
     
         5 . The method of  claim 1 , wherein the nucleotide sequence in (a) comprises a nucleotide sequence encoding the amino acid sequence of SEQ ID NO: 6 or comprises the nucleotide sequence of SEQ ID NO: 5. 
     
     
         6 . The method of  claim 1 , wherein the nucleotide sequence in (b) encodes a full-length RSV N nucleocapsid protein and a full-length RSV M2 matrix protein. 
     
     
         7 . The method of  claim 1 , wherein the nucleotide sequence in (b) is from strain A2. 
     
     
         8 . The method of  claim 1 , wherein the nucleotide sequence in (b) comprises a nucleotide sequence encoding the amino acid sequence of SEQ ID NO: 35; or comprises the nucleotide sequence of SEQ ID NO: 34. 
     
     
         9 . The method of  claim 1 , wherein the nucleotide sequence in (b) comprises a nucleotide sequence encoding the amino acid sequence of SEQ ID NO: 10; or comprises the nucleotide sequence of SEQ ID NO: 9. 
     
     
         10 . The method of  claim 1 , wherein the nucleotide sequence in (b) comprises a nucleotide sequence encoding the amino acid sequence of SEQ ID NO: 33; or comprises the nucleotide sequence of SEQ ID NO: 32. 
     
     
         11 . The method of  claim 1 , wherein the nucleotide sequence in (b) comprises a nucleotide sequence encoding the amino acid sequence of SEQ ID NO: 14; or comprises the nucleotide sequence of SEQ ID NO: 13. 
     
     
         12 . The method of  claim 1 , wherein the nucleotide sequence in (b) further encodes a self-cleaving protease domain between the antigenic determinants of the RSV N nucleocapsid and the RSV M2 matrix proteins. 
     
     
         13 . The method of  claim 12 , wherein the nucleotide sequence in (c) encodes a full-length RSV G membrane glycoprotein. 
     
     
         14 . The method of  claim 13 , wherein the nucleotide sequence in (c) is from RSV strain A2. 
     
     
         15 . The method of  claim 14 , wherein the nucleotide sequence in (c) comprises a nucleotide sequence encoding the amino acid sequence of SEQ ID NO: 2 or comprises the nucleotide sequence of SEQ ID NO: 1. 
     
     
         16 . The method of  claim 15 , wherein the MVA used for generating the recombinant MVA is MVA-BN deposited at the European Collection of Cell Cultures (ECACC) under number V00083008. 
     
     
         17 . The method of  claim 12 , wherein the self-cleaving protease domain has the amino acid sequence set forth in SEQ ID NO:12.

Join the waitlist — get patent alerts

Track US2021196814A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.