Opendata, web and dolomites

ImmunoStem SIGNED

Dissecting and Overcoming Innate Immune Barriers for Therapeutically Efficient Hematopoietic Stem Cell Gene Engineering

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 ImmunoStem project word cloud

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

mere    progress    host    disorders    single    therapies    doses    breaking    trials    restrict    recognition    cells    engineering    significantly    counteract    tip    human    gene    instruct    editing    builds    hurdle    manipulating    prevent    potentially    immune    cutting    culture    outcomes    efficiencies    autoimmune    direct    components    cell    pathogen    implications    ground    clinically    sensors    hsc    manipulation    variability    stem    vectors    completion    sustainable    effectors    action    levels    hematopoietic    nucleic    successful    paradigms    first    infectious    broadly    crosstalk    small    edge    fight    nevertheless    thorough    innovative    acid    ex    primitive    efficiency    exportable    antiviral    therapy    molecules    technologies    mitigate    efficient    iceberg    compartment    clinical    vivo    plethora    platforms    viral    mechanisms    hampering    broad    individual    discovered    vector    expose    blocks    sensing    genetic    diseases    potently    lentiviral    transfer    prolonged    innate    modification   

Project "ImmunoStem" 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 1˙994˙375 €
 EC max contribution 1˙994˙375 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-COG
 Funding Scheme ERC-COG
 Starting year 2019
 Duration (year-month-day) from 2019-03-01   to  2024-02-29

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    OSPEDALE SAN RAFFAELE SRL IT (MILANO) coordinator 1˙994˙375.00

Map

 Project objective

The low gene manipulation efficiency of human hematopoietic stem cells (HSC) remains a major hurdle for sustainable and broad clinical application of innovative therapies for a wide range of disorders. Indeed, high vector doses and prolonged ex vivo culture are still required for clinically relevant levels of gene transfer even with the most established lentiviral vector-based delivery platforms. Current and emerging gene transfer and editing technologies expose HSC to components potentially recognized by host antiviral factors and nucleic acid sensors that likely restrict their genetic engineering and contribute to broad individual variability in clinical outcomes observed in recent gene therapy trials. Nevertheless, specific effectors are yet to be identified in HSC. We have recently identified an antiviral factor that potently blocks gene transfer in HSC and have discovered small molecules that efficiently counteract it. This is the first example of how manipulating a single host factor can significantly impact gene transfer efficiencies in HSC but likely represents the mere tip of the iceberg of the plethora of innate sensing mechanisms potentially hampering genetic manipulation of this primitive cell compartment. This proposal aims to identify the antiviral factors and innate sensing pathways that prevent efficient modification of HSC and to mitigate their effects using methods developed through a thorough understanding of their mechanisms of action. My approach builds on the innovative concept that understanding the crosstalk between HSC and viral vectors will instruct us on which immune sensors and effectors to avoid and how, with direct implications for all gene engineering technologies. Successful completion of this project will deliver broadly exportable novel paradigms of innate pathogen recognition that will allow ground-breaking progress in the development of cutting-edge cell and gene therapies and to fight infectious and autoimmune diseases.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "IMMUNOSTEM" 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 "IMMUNOSTEM" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

MATCH (2020)

Discovering a novel allergen immunotherapy in house dust mite allergy tolerance research

Read More  

TORYD (2020)

TOpological many-body states with ultracold RYDberg atoms

Read More  

Mu-MASS (2019)

Muonium Laser Spectroscopy

Read More