Method of conferring a protective immune response to norovirus

a technology of immune response and norovirus, which is applied in the field of vaccines, can solve the problems of lack of reproducibility, no studies have reported being able to achieve protective immunity against i>norovirus/i>, etc., and achieves the effects of enhancing immune response, enhancing antigen uptake, and increasing antigen retention tim

Inactive Publication Date: 2010-10-21
TAKEDA VACCINES MONTANA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0009]In some embodiments, the vaccine further comprises a delivery agent, which functions to enhance antigen uptake, provide a depot effect, increase antigen retention time at the site of delivery, or enhance the immune response through relaxation of cellular tight junctions at the delivery site. The delivery agent can be a bioadhesive, preferably a mucoadhesive selected from the group consisting of dermat...

Problems solved by technology

Consequently, VLPs mimic the functional interactions of the virus with cellular receptors, thereby eliciting an appropriate host immune response while lacking ...

Method used

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  • Method of conferring a protective immune response to norovirus
  • Method of conferring a protective immune response to norovirus
  • Method of conferring a protective immune response to norovirus

Examples

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example 1

GLP Toxicity Study of Norovirus Vaccine Formulations in Rabbits

[0070]The purpose of this study was to evaluate the potential toxicity of a Norwalk virus-virus-like particle (NV-VLP) vaccine following three intranasal doses in rabbits. The NV-VLP vaccine contained (per 10 mg dry powder) 25 μg of a Genogroup I VLP, 25 μg MPL, 7 mg chitosan glutamate, 1.475 mg mannitol, and 1.475 mg sucrose. The study was conducted over an eight week period. The persistence, reversibility, or delayed onset of any effects were assessed after a four-week, no-treatment recovery interval. Sixty New Zealand White rabbits (30 / sex) were randomly assigned to three groups (10 rabbits / sex / group). Group 1 animals were not dosed (i.e. naïve). Group 2 animals were administered 10 mg / nostril (20 mg total) of placebo (i.e. adjuvant / excipient: MPL, chitosan, sucrose, and mannitol). Group 3 animals were administered 10 mg / nostril (20 mg total) of NV-VLP vaccine, which represented 25 μg of antigen per nostril (50 μg tot...

example 2

Dose Escalation Safety Study of Norwalk Vaccine Formulation in Humans (LV01-101 Study)

[0074]A double-blind, controlled, dose-escalation phase 1 study of the safety and immunogenicity of a Norovirus genogroup 1 vaccine was conducted. The vaccine consisted of lyophilized Norwalk virus-like particles (VLPs) in a dry powder matrix designed for intranasal administration. Vaccines included healthy adult volunteers who were H type 1 antigen secretors. The rationale for enrollment of H type 1 antigen secretors is that H type 1 antigen secretors are susceptible to Norwalk viral infections while non-secretors are resistant. Saliva was collected from volunteers to determine H type 1 antigen secretor status. As a control, 2 additional volunteers at each dosage level received matrix alone. The dry powder matrix included 25 μg MPL® adjuvant, 7 mg chitosan, 1.5 mg mannitol, and 1.5 mg sucrose. Volunteers were dosed on days 0 and 21 and were required to keep a 7-day diary of symptoms after each dos...

example 3

Safety and Immunogenicity Study of Two Dosages of Intranasal Norwalk VLP Vaccine in Humans (LV01-102 Study)

[0087]A randomized, double blind, multi-center study in healthy adults was conducted to compare the safety and immunogenicity of two dosage levels (50 μg and 100 μg) of a Norwalk virus-like particle (VLP) vaccine with adjuvant / excipients and placebo controls (empty device). The vaccine consisted of Norwalk virus-like particles (VLPs) in a dry powder matrix designed for intranasal administration as described in Example 2. Vaccines included healthy adult volunteers ages 18-49 who were H type 1 antigen secretors. Saliva was collected from volunteers to determine H type 1 antigen secretor status. Further, only subjects whose blood type was A or O (not type B or AB) were included in the study as those with B blood type are reported to be less susceptible to Norwalk infection (Glass et al. (2009) N. Engl. J. Med., Vol. 361: 1776-1785). The human volunteers were randomly assigned to o...

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Abstract

The present invention relates to vaccine compositions comprising Norovirus antigens and adjuvants, in particular, mixtures of monovalent VLPs and mixtures of multivalent VLPs, and to methods of conferring protective immunity to Norovirus infections in a human subject.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation-in-part of U.S. application Ser. No. 12 / 678,813, filed Mar. 18, 2010, which is a national stage application of International Application No. PCT / US2008 / 076763, filed Sep. 18, 2008, which claims the benefit of priority of U.S. Provisional Application No. 60 / 973,389, filed Sep. 18, 2007, and U.S. Provisional Application No. 60 / 986,826, filed Nov. 9, 2007, all of which are herein incorporated by reference in their entireties.STATEMENT OF GOVERNMENT SUPPORT[0002]This invention was produced with government support from the US Army Medical Research and Material Command, under contract number W81XWH-05-C-0135. The government may have certain rights to the invention.FIELD OF THE INVENTION[0003]The invention is in the field of vaccines, particularly vaccines for Noroviruses. In addition, the invention relates to methods of preparing vaccine compositions and methods of inducing a protective immune response.BACKGRO...

Claims

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Application Information

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IPC IPC(8): A61K39/125A61P31/14
CPCA61K39/125A61K2039/5258A61K39/12C12N2770/16034A61K2039/55572A61K2039/57A61K2039/543A61P31/14
Inventor RICHARDSON, CHARLESVEDVICK, THOMAS S.FOUBERT, THOMAS R.
Owner TAKEDA VACCINES MONTANA
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