Norovirus immunogens and related materials and methods

Patent metadata

Field	Value
Publication number	US-9402891-B2
Application number	US-201214124499-A
Country	US
Kind code	B2
Filing date	Jun 8, 2012
Priority date	Jun 8, 2011
Publication date	Aug 2, 2016
Grant date	Aug 2, 2016

Abstract

The inventors have successfully developed a recombinant vesicular stomatitis virus which expresses the major capsid protein of human norovirus. Infection of mammalian cells with the recombinant vesicular stomatitis virus resulted in production of high level of human norovirus virus-like particles. Importantly, the inventors further demonstrated that recombinant vesicular stomatitis virus expressing the major capsid protein of human norovirus displayed attenuated virulence in mice and elicited a high level of human norovirus-specific humoral, cellular, and mucosal immune responses in mice model. Therefore, norovirus-immunogenic compositions are herein provided, as are materials and methods useful to make and use the compositions.

First claim

The invention claimed is:

1. A live recombinant vesicular stomatitis virus (VSV)-vector vaccine composition for a human norovirus, the composition comprising a virus encoding a foodborne viral immunogen inserted between glycoprotein and polymerase genes of a VSV genome, wherein the foodborne viral immunogen is a major capsid protein of a norovirus, or an immunogenic fragment thereof;
wherein the insertion attenuates or eliminates VSV virulence,
wherein the encoded foodborne virus immunogen forms a virus-like particle (VLP) when the norovirus immunogen is expressed, and
wherein the VLP is capable of being formed in vivo subsequent to norovirus immunogen expression from the VSV-vector vaccine composition.

2. The composition of claim 1 , wherein the composition is capable of partially or fully protecting a mammal susceptible to the foodborne virus from infection by the foodborne virus.

3. The composition of claim 1 , wherein the recombinant VSV composition comprises an oral composition.

4. The composition of claim 3 , wherein the oral composition is a single dose.

5. The composition of claim 1 , wherein the recombinant VSV composition comprises a nasal composition.

6. The composition of claim 5 , wherein the nasal composition is a single dose.

7. A method of eliciting an immune response in a mammal comprising: administering to a mammal a recombinant vesicular stomatitis virus (VSV)-vector vaccine composition for a human norovirus, the composition comprising a virus encoding a foodborne viral immunogen inserted between glycoprotein and polymerase genes of a VSV genome, wherein the foodborne viral immunogen is a major capsid protein of a norovirus or an immunogenic fragment thereof;
wherein the insertion attenuates or eliminates VSV virulence,
wherein the encoded foodborne virus immunogen forms a virus-like particle (VLP) when the norovirus immunogen is expressed, and
wherein the VLP is capable of being formed in vivo subsequent to norovirus immunogen expression from the VSV-vector vaccine composition.

8. The method of claim 7 wherein the recombinant VSV composition is administered orally.

9. The method of claim 7 wherein the recombinant VSV composition is administered intranasally.

10. The method of claim 7 , wherein the elicited immune response partially or fully protects the mammal from infection by the foodborne virus.

11. A method of preparing a pharmaceutical composition for immunization of an individual in need of immunization comprising:
Expressing a recombinant vesicular stomatitis virus vector (VSV) so as to form virus-like particles;
and mixing said virus-like particles with a suitable excipient or carrier, thereby forming a pharmaceutical composition;

wherein the recombinant VSV vector comprises a VSV genome and a nucleic acid sequence encoding a norovirus immunogen;
wherein the norovirus immunogen is a major capsid protein or an immunogenic fragment of a norovirus;
wherein the encoded immunogen forms a virus-like particle (VLP) when expressed; and,
wherein the VLP is capable of being continuously expressed in vivo by the VSV-vector composition.

12. The method of claim 11 wherein the immunogen-encoding nucleic acid molecule is inserted between glycoprotein and polymerase genes of the viral genome.

13. The method of claim 11 wherein the pharmaceutical composition is formulated for oral administration.

14. The method of claim 11 wherein the pharmaceutical composition is formulated for intranasal administration.

Assignees

• Li Jianrong
• Ma Yuanmei
• Ohio State Innovation Foundation

Inventors

• Li Jianrong
• Ma Yuanmei

Classifications

• A61K39/12 Primary

  Viral antigens · CPC title

• A61K2039/575

  humoral response · CPC title

• C12N2770/16034

  Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title

• A61K2039/5252

  inactivated (killed) · CPC title

• C12N2760/00034

  Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title