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VACCIBIOME SIGNED

Cancer Vaccines and Gut Microbiome: a rational approach to optimize cancer immunotherapy

Total Cost €

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EC-Contrib. €

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Partnership

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 VACCIBIOME project word cloud

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

engineered    interplay    cells    mice    processed    goals    composition    cd4    first    underlying    bifidobacterial    exome    cd8    presenting    cross    antigens    cell    model    select    showed    personalized    presented    neo    milestone    optimize    light    cancer    ultimate    fraction    l1    epitopes    oral    patients    meta    react    models    immune    microbial    mutations    vaccine    anti    vaccines    intends    cocktails    reactive    influences    substantially    power    tumor    originates    antibody    immunotherapies    animal    predicted    gnotobiotic    gavages    negatively    repertoire    potentiators    effectiveness    immunity    gut    transcriptome    humans    formulate    containing    deep    therapy    therapeutic    peripheral    undergoing    reacting    tools    lines    modulate    omics    discoveries    normal    immunotherapy    positively    prognostic    microbiome    mimicry    depending    mechanisms    shed    elucidated    species    originate    combination    antigen    hypothesis    mm    criteria    molecular    pd    epitope    mouse   

Project "VACCIBIOME" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITA DEGLI STUDI DI TRENTO 

Organization address
address: VIA CALEPINA 14
city: TRENTO
postcode: 38122
website: www.unitn.it

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 Italy [IT]
 Total cost 2˙450˙000 €
 EC max contribution 2˙450˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-ADG
 Funding Scheme ERC-ADG
 Starting year 2019
 Duration (year-month-day) from 2019-09-01   to  2024-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITA DEGLI STUDI DI TRENTO IT (TRENTO) coordinator 1˙542˙500.00
2    FONDAZIONE TOSCANA LIFE SCIENCES IT (SIENA) participant 907˙500.00

Map

 Project objective

This proposal intends to shed light on the interplay between cancer immunity and gut microbiome as a way to optimize personalized cancer vaccines and immunotherapy. The project originates from two milestone discoveries. First, to be effective cancer immunotherapies have to target CD4/CD8 T cell neo-epitopes, which originate from tumor mutations. Second, the gut microbiome influences the effectiveness of anti-PD-1/PD-L1 antibody immunotherapy both in animal models and in humans. We also recently showed in a mouse model that oral gavages with Bifidobacterial cocktails improved the therapeutic power of neo-epitope-based cancer vaccines. How microbiome affects anti-cancer immunity has not been fully elucidated yet and a deep understanding of the underlying mechanisms has the potential to substantially improve cancer immunotherapy. Since microbiome antigens are processed and presented by antigen-presenting cells and microbiome-induced T cells represent large fraction of the peripheral T cell repertoire, our hypothesis is that this large repertoire includes T cells which cross-react with cancer neo-epitopes (“molecular mimicry (MM)”). Depending upon the composition of gut microbiome, cross-reacting T cells can positively or negatively modulate anti-tumor immunity. To demonstrate the role of MM in cancer immunity this project intends (i) to select the cross-reactive T cell epitopes as predicted by meta-omics analysis of gut microbiome and exome/transcriptome analysis of cancer cell lines, (ii) to formulate vaccines containing different combination of cross-reactive epitopes, and (iii) to test vaccine anti-tumor activities in normal mice, gnotobiotic mice and mice with engineered microbiome. The ultimate goals are: 1) to provide new criteria for neo-epitope selection in personalized cancer vaccines, 2) to develop prognostic tools based on microbiome analysis, and 3) to define microbial species to be used as immune-potentiators in patients undergoing cancer therapy.

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

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