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VIVAVE

Viral Vaccine Vectors in Personalized Medicine

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 VIVAVE project word cloud

Explore the words cloud of the VIVAVE project. It provides you a very rough idea of what is the project "VIVAVE" about.

relapse    patients    therapies    millions    maintained    worldwide    genes    surveillance    cancer    grow    aggressive    replication    release    latency    stage    humans    survive    slowly    time    lymphoma    successful    tumors    infected    expressed    profile    virus    condemned    therapy    promotes    human    cells    exceedingly    fills    animal    expensive    provides    iatrogenic    aborted    monitored    depot    versatile    tissue    life    decades    innocuous    immunity    vaccine    minimal    clinical    rapid    few    class    free    generally    infection    blocking    residual    options    grows    elimination    safe    bout    vector    nuclei    levels    poorly    pipeline    viral    lasting    sustained    released    melanoma    strike    host    active    vectors    arising    immune    relapses    people    uniquely    pathogens    counterparts    establishes    antigen    disease    combines    stimulate    vaccines    developers    hence    deterrence    neoplastic    tumor    modified    faster    culture    replicate   

Project "VIVAVE" data sheet

The following table provides information about the project.

Coordinator
HELMHOLTZ-ZENTRUM FUR INFEKTIONSFORSCHUNG GMBH 

Organization address
address: INHOFFENSTRASSE 7
city: BRAUNSCHWEIG
postcode: 38124
website: www.helmholtz-hzi.de

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 149˙858 €
 EC max contribution 149˙858 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-PoC
 Funding Scheme ERC-POC
 Starting year 2017
 Duration (year-month-day) from 2017-02-01   to  2018-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    HELMHOLTZ-ZENTRUM FUR INFEKTIONSFORSCHUNG GMBH DE (BRAUNSCHWEIG) coordinator 149˙858.00

Map

 Project objective

Melanoma and lymphoma are tumors that strike millions of people worldwide and require aggressive and expensive therapies. Numerous therapies are already being used or in the pipeline, yet all of them focus on the rapid elimination of the active neoplastic process. They do not provide options for long-term surveillance and deterrence of minimal residual disease, that is, of cancer relapse arising from the few tumor cells that survive the aggressive bout of therapy. Therefore, even patients considered cancer-free upon successful therapy are monitored over decades for potential relapses and condemned to a life of uncertainty. I propose to develop a novel class of versatile tumor vaccines for long-term surveillance of tumors based on a modified virus vector. Our modified viral vector combines an exceedingly safe profile with robust and long-lasting immunity. Several developers have focused on human virus vaccine vectors that grow poorly in tissue culture, and as human pathogens, present iatrogenic concerns. Our modified viral vector system grows faster in animal cells than human counterparts, but cannot replicate in human cells. Therefore, our vector system is generally considered innocuous for humans. The replication in human cells is aborted at the early stage of infection, but immediate-early genes are expressed at robust levels, and thus may stimulate immune responses. Our modified viral vector system establishes latency and is maintained for life in the nuclei of infected cells, where they release low levels of antigen for the life of the host. Thus, it provides a depot of antigen that is slowly released over time and promotes the uniquely strong and sustained immunity. Our approach is unique in its design to provide long-term immune surveillance of tumor cells, and thus in blocking relapses. Hence, we propose to develop a unique product that fills an important clinical need.

 Publications

year authors and title journal last update
List of publications.
2019 Elham Beyranvand Nejad, Robert B. Ratts, Eleni Panagioti, Christine Meyer, Jennifer D. Oduro, Luka Cicin-Sain, Klaus Früh, Sjoerd H. van der Burg, Ramon Arens
Demarcated thresholds of tumor-specific CD8 T cells elicited by MCMV-based vaccine vectors provide robust correlates of protection
published pages: , ISSN: 2051-1426, DOI: 10.1186/s40425-019-0500-9
Journal for ImmunoTherapy of Cancer 7/1 2019-07-18

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The information about "VIVAVE" are provided by the European Opendata Portal: CORDIS opendata.

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