Opendata, web and dolomites

THAT IS HUNT SIGNED

Triggering Haematological Adoptive T-cell Immunotherapy Strategies by HUnting Novel T-cellreceptors

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 THAT IS HUNT project word cloud

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

antigen    tcrs    chains    career    fellowship    tumors    genome    cells    streamline    complementary    biology    differentiate    hla    intrinsic    fingerprint    lab    off    isolate    treatment    cell    leukemia    issue    urgently    expressing    endogenous    acquire    lymphocytes    full    potent    hunting    unfortunately    hypothesize    restrictions    knowhow    shelf    patients    antigens    myeloid    immune    avidity    identification    editing    repertoire    opened    immunotherapeutic    scientific    expertise    aml    successfully    recent    gene    combine    mispairing    immunoprofiling    immunotherapy    landscape    therapy    receptor    cancer    hosting    protocol    technologies    edge    first    reactive    broad    transfer    awarding    clinical    researcher    innovative    skills    exogenous    hampered    rendering    solid    limiting    specificities    cutting    blasts    encouraging    generation    opportunity    presenting    limited    functional    library    sequencing    acute    tcr    bottleneck    engineered    applicability    tumor    ligandome    widen    genetic   

Project "THAT IS HUNT" data sheet

The following table provides information about the project.

Coordinator
OSPEDALE SAN RAFFAELE SRL 

Organization address
address: VIA OLGETTINA 60
city: MILANO
postcode: 20132
website: www.hsr.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 168˙277 €
 EC max contribution 168˙277 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2016
 Funding Scheme MSCA-IF-EF-SE
 Starting year 2018
 Duration (year-month-day) from 2018-01-01   to  2019-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    OSPEDALE SAN RAFFAELE SRL IT (MILANO) coordinator 168˙277.00

Map

 Project objective

Recent encouraging clinical results obtained with engineered T lymphocytes and increasing advances in the genome editing field, have opened new opportunities for T-cell receptor (TCR) gene therapy as an immunotherapeutic approach for cancer. Unfortunately, the broad applicability of this treatment is still hampered by the possible mispairing of exogenous/endogenous TCR chains and by the limited number of high avidity tumor-specific TCRs. While the first issue has been successfully addressed by the hosting lab with the development a TCR gene editing protocol, the identification of novel tumor-specific TCRs is urgently required and this is the aim of my research proposal. We have the unique opportunity to combine the highly complementary expertise of the hosting lab in T-cell biology/genetic transfer and of the applicant on immune repertoire sequencing. We will target acute myeloid leukemia (AML) and hypothesize that by exploiting intrinsic features of AML (i.e. ability of AML blasts to differentiate into potent antigen presenting cells expressing tumor antigens), the functional fingerprint induced by AML on tumor-reactive T-cells, and cutting-edge technologies (i.e. next generation sequencing; ligandome landscape analysis), we will provide a comprehensive immunoprofiling of tumor-specific T-cells and isolate tumor TCR specificities. Results obtained in this study will streamline TCR hunting studies in solid tumors, leading to the generation of a TCR library for different antigens and HLA restrictions, thus rendering TCR gene editing an innovative off-the-shelf treatment available for a high number of cancer patients. Awarding this fellowship will greatly enhance researcher’s career not only by providing the opportunity to widen scientific knowhow and acquire new skills, but also by enabling the researcher to address a major bottleneck currently limiting the full exploitation of the rapidly growing field of cancer immunotherapy.

 Publications

year authors and title journal last update
List of publications.
2019 Maddalena Noviello, Francesco Manfredi, Eliana Ruggiero, Tommaso Perini, Giacomo Oliveira, Filippo Cortesi, Pantaleo De Simone, Cristina Toffalori, Valentina Gambacorta, Raffaella Greco, Jacopo Peccatori, Monica Casucci, Giulia Casorati, Paolo Dellabona, Masahiro Onozawa, Takanori Teshima, Marieke Griffioen, Constantijn J. M. Halkes, J. H. F. Falkenburg, Friedrich Stölzel, Heidi Altmann, Martin B
Bone marrow central memory and memory stem T-cell exhaustion in AML patients relapsing after HSCT
published pages: , ISSN: 2041-1723, DOI: 10.1038/s41467-019-08871-1
Nature Communications 10/1 2020-03-05

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "THAT IS HUNT" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "THAT IS HUNT" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

RipGEESE (2020)

Identifying the ripples of gene regulation evolution in the evolution of gene sequences to determine when animal nervous systems evolved

Read More  

EngPTC2 (2019)

Exploring new technologies for the next generation pulse tube cryocooler below 2K

Read More  

GrowthDevStability (2020)

Characterization of the developmental mechanisms ensuring a robust symmetrical growth in the bilateral model organism Drosophila melanogaster

Read More