IP Library › Granted Patent US 11,896,636
Granted Patent B2
US 11,896,636 · App. 14/130,899 · Granted Feb 13, 2024

Immunogenic combination compositions and uses thereof

Inventors: Andrew Geall (Littleton, MA); Ethan Settembre (Lexington, MA)
Assignee: GLAXOSMITHKLINE BIOLOGICALS SA
A61K35/763A61K35/76A61K39/12A61K39/23A61K39/245A61K2039/5258A61K2039/53A61K2039/55566A61K2039/70C12N2710/16134C12N2750/14223C12N2750/14234C12N2770/36143
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Quick Facts
Patent No.
US 11,896,636
App. No.
14/130,899
Granted
Feb 13, 2024
Kind
B2
Abstract

This invention generally relates to immunogenic compositions that comprise an RNA component and a polypeptide component. Immunogenic compositions that deliver antigens in two different forms—a first antigen from a pathogen, in RNA-coded form; and a second antigen from a different pathogen, in polypeptide form—are effective in inducing immune response to both pathogens.

Claims (22)

1. An immunogenic composition comprising:

(i) a first polypeptide antigen derived from the group consisting of a viral pathogen and a bacterial pathogen, and

(ii) a self-replicating RNA molecule encapsulated within a liposome, wherein said self-replicating RNA molecule cannot induce production of infectious viral particles, encodes a second polypeptide antigen from a viral pathogen, and can promote T cell-mediated immunity as well as humoral immunity to both first and second antigens,

wherein said first and second antigens are antigens from different pathogens,

wherein the self-replicating RNA molecule is not encapsulated in a virus-like particle; and

wherein the liposome encapsulating the self-replicating RNA molecule does not include capsid protein or envelope glycoproteins.

2. The immunogenic composition of claim 1 , wherein said second polypeptide antigen is a Cytomegalovirus (CMV) antigen.

3. The immunogenic composition of claim 1 , wherein said first polypeptide antigen is in the form of a virus-like particle (VLP).

4. The immunogenic composition of claim 1 , wherein said first polypeptide antigen is a soluble polypeptide and said second polypeptide antigen is a soluble or membrane anchored polypeptide.

5. The immunogenic composition of claim 1 , wherein the self-replicating RNA is an alphavirus-derived RNA replicon.

6. The immunogenic composition of claim 1 , wherein the self-replicating RNA molecule comprises one or more modified nucleotides.

7. The immunogenic composition of claim 1 , wherein the first polypeptide antigen and second polypeptide antigen are both viral antigens.

8. The immunogenic composition of claim 7 , wherein one viral antigen is an antigen from CMV.

9. An immunogenic composition comprising:

(i) a first viral polypeptide antigen, and

(ii) a self-replicating RNA molecule encapsulated within a liposome, wherein said self-replicating RNA molecule cannot induce production of infectious viral particles, encodes a second viral polypeptide antigen from a viral pathogen, and can promote T cell-mediated immunity as well as humoral immunity to both first and second antigens,

wherein said first and second antigens are antigens from different viral pathogens,

wherein one viral antigen is a Parvovirus antigen.

10. The immunogenic composition of claim 9 , wherein the Parvovirus antigen comprises an amino acid sequence encoded by SEQ ID NO: 25 or 26.

11. The immunogenic composition of claim 1 , further comprising an adjuvant.

12. An immunogenic composition comprising: (i) a Parvovirus polypeptide antigen, and (ii) a self-replicating RNA molecule that encodes a CMV polypeptide antigen.

13. A method for inducing an immune response in a subject comprising administering to a subject in need thereof a therapeutically effective amount of a composition according to claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 22, 2016
From: NOVARTIS AG
To: GLAXOSMITHKLINE BIOLOGICALS SA
Reel/Frame 038982/0776 →
Continuity (2)
Provisional Application 61505093 · Jul 6, 2011
Related Publication 20140227346A1 · Aug 14, 2014