IP Library › Granted Patent US 9,730,997
Granted Patent B2
US 9,730,997 · App. 14/463,831 · Granted Aug 15, 2017

Alphavirus vectors for respiratory pathogen vaccines

Inventors: Silvia Perri (Castro Valley, CA); John Polo (Danville, CA); Yasushi Uematsu (Siena, IT); Catherine Greer (Oakland, CA)
Assignee: Novartis Vaccines and Diagnostics, Inc.
A61K39/12A61K39/145A61K39/155C12N15/86A61K2039/5252A61K2039/5256A61K2039/53A61K2039/543A61K2039/545A61K2039/55544A61K2039/55566A61K2039/70C12N2760/16122C12N2760/16134C12N2760/18322C12N2760/18334C12N2760/18522C12N2760/18534C12N2760/18622C12N2760/18634C12N2770/20022C12N2770/20034C12N2770/36143C12N2830/20C12N2830/60C12N2840/20C12N2840/203
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Quick Facts
Patent No.
US 9,730,997
App. No.
14/463,831
Granted
Aug 15, 2017
Kind
B2
Abstract

Described herein are compositions and methods for stimulating an immune response to one or more proteins derived from one or more respiratory pathogens. In particular, the invention relates to alphavirus replicons, alphavirus vector constructs, alphavirus replicon particles expressing one or more antigens derived from one or more respiratory pathogens as well as to method of making and using these immunogenic compositions.

Claims (22)

1. An immunogenic composition comprising:

(a) an alphavirus replicon vector comprising:

(i) a first heterologous nucleic acid sequence encoding a first protein antigen from a first influenza virus, and

(ii) a second heterologous nucleic acid sequence encoding a second protein antigen from a second influenza virus, wherein said second heterologous nucleic acid sequence is different from said first heterologous nucleic acid sequence; and

(b) a pharmaceutically acceptable carrier, diluent, or excipient.

2. The immunogenic composition of claim 1 , wherein said first and second protein antigens each is independently selected from the group consisting of: a hemagglutinin (HA), a neuraminidase (NA), a nucleocapsid (NP), a matrix protein (M1), an ion channel protein (M2), NS 1, NS2, PB1, PB2, PA, an immunogenic fragment thereof, and a combination thereof.

3. The immunogenic composition of claim 1 , wherein said first protein antigen is an influenza hemagglutinin (HA) or immunogenic fragment thereof.

4. The immunogenic composition of claim 3 , wherein said first influenza virus is a subtype selected from the group consisting of H1, H2, H3, H4, H5, H6, H7, H8, H9, H10, H11, H12, H13, H14, and H15 subtypes.

5. The immunogenic composition of claim 1 , wherein said second protein antigen is an influenza neuraminidase (NA) or immunogenic fragment thereof.

6. The immunogenic composition of claim 1 , wherein said second influenza virus is a subtype selected from the group consisting of N1, N2, N3, N4, N5, N6, N7, N8, and N9 subtypes.

7. The immunogenic composition of claim 1 , wherein said first protein antigen is an influenza hemagglutinin or immunogenic fragment thereof, and said second protein antigen is an influenza neuraminidase or immunogenic fragment thereof.

8. The immunogenic composition of claim 1 , wherein said first and second influenza viruses each is independently a pandemic, potentially pandemic, or interpandemic influenza virus strain.

9. The immunogenic composition of claim 1 , wherein said first protein antigen is an influenza hemagglutinin (HA) or immunogenic fragment thereof from a pandemic, potentially pandemic, or interpandemic influenza virus strain.

10. The immunogenic composition of claim 1 , wherein said first protein antigen is an influenza hemagglutinin (HA) or immunogenic fragment thereof from a combination of (1) a pandemic or potentially pandemic influenza virus strain, and (2) an interpandemic influenza virus strain.

11. The immunogenic composition of claim 1 , wherein the first heterologous nucleic acid sequence is operably linked to a first alphavirus subgenomic promoter.

12. The immunogenic composition of claim 1 , wherein the second heterologous nucleic acid sequence is operably linked to a second alphavirus subgenomic promoter.

13. The immunogenic composition of claim 1 , wherein the first, second, or both heterologous nucleic acid sequences further comprise an internal ribosome entry site (IRES).

14. The immunogenic composition of claim 1 , wherein the alphavirus replicon vector is vector derived from an alphavirus selected from the group consisting of: a Sindbis virus, a Semliki Forest virus, a Venezuelan equine encephalitis virus, and a Ross River virus.

15. A method of stimulating an immune response in a mammal, comprising administering an immunogenic composition of claim 1 to said mammal.

16. The method of claim 15 , further comprising administering a second immunogenic composition to said mammal, wherein the second immunogenic composition comprises:

(a) a protein antigen or immunogenic fragment thereof, from the same first influenza strain; and

a pharmaceutically acceptable carrier, diluent, or excipient.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2014
From: PERRI, SILVIA; POLO, JOHN; GREER, CATHERINE
To: NOVARTIS VACCINES AND DIAGNOSTICS, INC.
Reel/Frame 033839/0185 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2014
From: UEMATSU, YASUSHI
To: NOVARTIS VACCINES AND DIAGNOSTICS SRL.
Reel/Frame 033839/0232 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2014
From: NOVARTIS VACCINES AND DIAGNOSTICS SRL
To: NOVARTIS VACCINES AND DIAGNOSTICS, INC.
Reel/Frame 033839/0264 →
Continuity (5)
Continuation 12791140 · Jun 1, 2010
Division 11597347
Provisional Application 60573433 · May 21, 2004
Provisional Application 60643737 · Jan 12, 2005
Related Publication 20150024002A1 · Jan 22, 2015