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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.

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

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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