IP Library Granted Patent US 9,017,691
Granted Patent B2
US 9,017,691 · App. 13/130,018 · Granted Apr 28, 2015

Antiviral vaccines with improved cellular immunogenicity

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Quick Facts
Patent No.
US 9,017,691
App. No.
13/130,018
Granted
Apr 28, 2015
Kind
B2
Abstract

The invention provides compositions, methods, and kits for the treatment or prevention of viral infections. The polyvalent (e.g., 2-valent) vaccines described herein incorporate computationally-optimized viral polypeptides that can increase the diversity or breadth and depth of cellular immune response in vaccinated subjects.

Claims (33)

1. An immunogenic composition comprising at least two distinct optimized viral polypeptides, wherein said optimized viral polypeptides correspond to the same viral gene product, wherein the viral gene product is selected from the group consisting of gag, pol, and env, and

wherein the at least two distinct optimized gag polypeptides are selected from any one or more of the groups:

(a) SEQ ID NO: 3 and 4, (b) SEQ ID NO: 3, and 15 (c) SEQ ID NO: 4 and 15;

wherein the at least two distinct optimized pol polypeptides are selected from any one or more of the groups:

(a) SEQ ID NO: 12 and 13, (b) SEQ ID NO: 12 and 14, (c) SEQ ID NO: 13 and 14; and

wherein the at least two distinct optimized env polypeptides are selected from any one or more of the groups:

(a) SEQ ID NO: 9 and 10, (b) SEQ ID NO: 9 and 11, (c) SEQ ID NO: 10 and 11.

2. The immunogenic composition of claim 1 , wherein said mammal is a human.

3. The immunogenic composition of claim 1 , wherein said immunogenic composition elicits a cellular immune response against said viral gene product.

4. The immunogenic composition of claim 1 , wherein said at least two optimized gag viral polypeptides comprise an amino acid sequence having the sequences set forth in each of SEQ ID NO:3 and 4.

5. The immunogenic composition of claim 1 , wherein said at least two optimized pol viral polypeptides comprise an amino acid sequence having the sequences set forth in each of SEQ ID NO:12 and 13.

6. The immunogenic composition of claim 4 further comprising at least two optimized pol viral polypeptides, wherein said polypeptides comprise an amino acid sequence having the sequences set forth in each of SEQ ID NO:12 and 13.

7. The immunogenic composition of claim 6 further comprising at least two optimized env viral polypeptides, wherein said polypeptides comprise an amino acid sequence having the sequences set forth in each of SEQ ID NO:9 and 10.

8. The immunogenic composition of claim 1 , wherein said at least two distinct optimized viral polypeptides are encoded in a viral vector selected from the group consisting of adenovirus serotype 26 (Ad26), adenovirus serotype 34 (Ad34), adenovirus serotype 35 (Ad35), adenovirus serotype 48 (Ad48), er adenovirus serotype 5 HVR48 (Ad5HVR48), poxvirus, and modified vaccinia virus Ankara (MVA).

9. A method for inducing an HIV-1-specific immune response in a mammal comprising administering to said mammal the immunogenic composition of claim 1 .

10. A method of manufacturing the immunogenic composition of claim 1 comprising synthesizing said optimized viral polypeptides and combining said optimized viral polypeptides with a pharmaceutically acceptable carrier.

11. A kit comprising:

a) the immunogenic composition of claim 1 ;

b) a pharmaceutically acceptable carrier, excipient, or diluent;

c) instructions for the use thereof; and, optionally,

d) an adjuvant.

12. The immunogenic composition of claim 8 , wherein said vector is the Ad26 vector.

13. The immunogenic composition of claim 8 , wherein said vector is the MVA vector.

14. The immunogenic composition of claim 1 admixed with a pharmaceutically acceptable carrier, excipient, or diluent.

15. The immunogenic composition of claim 1 , wherein said at least two optimized env viral polypeptides comprise an amino acid sequence having the sequences set forth in each of SEQ ID NO:9 and 11.

16. A method for inducing an HIV-1-specific immune response in a mammal comprising administering to said mammal the immunogenic composition of claim 8 .

17. The method of claim 16 , wherein said vector is the Ad26 vector.

18. The method of claim 16 , wherein said vector is the MVA vector.

19. A polypeptide comprising the amino acid sequence of SEQ ID NO: 9.

20. A method for inducing an HIV-1-specific immune response in a mammal comprising administering to said mammal the immunogenic composition of claim 19 .

21. The method of claim 20 , wherein the mammal is a human.

22. The method of claim 21 , wherein said composition comprises a pharmaceutically acceptable carrier, excipient, or diluent.

23. The method of claim 16 , wherein said mammal is a human.

Assignments (3)
CONFIRMATORY LICENSE Recorded Sep 28, 2012
From: BETH ISRAEL DEACONESS MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029050/0964 →
CONFIRMATORY LICENSE Recorded Oct 6, 2011
From: LOS ALAMOS NATIONAL SECURITY
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 027025/0959 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2011
From: BAROUCH, DAN H.
To: BETH ISRAEL DEACONESS MEDICAL CENTER
Reel/Frame 026988/0083 →