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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.

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

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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