Opendata, web and dolomites

SYNKIT SIGNED

Synthetic Natural Killer Cells for Immunotherapy

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 SYNKIT project word cloud

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

shelf    ink    thereby    therapies    ing    broad    self    tumour    off    function    impaired    education    innovative    anti    triggers    engineering    vitro    cancer    nk    limited    combat    synkit    ipsc    successful    pluripotent    cell    pave    absence    natural    reduce    transfer    persistence    limitations    option    ipscs    bottlenecks    leukocyte    mechanism    host    killer    urging    tailor    antigen    worldwide    capacity    poor    synthetic    differentiation    escape    insights    intrinsic    platform    cells    possess    strategy    unravelled    immunotherapy    stem    lack    molecular    efficacy    death    hla    rejection    deletion    engineered    treatment    generation    allogeneic    attractive    human    setting    disarming    infusion    underlying    diminishing    tumours    modulates    completion    expand    immune    laboratory    ligands    complete    allogenicity    functional    genetic    transferred    introduction    missing    recipient    modulate    eliminate    deficient    prevent    recognition   

Project "SYNKIT" data sheet

The following table provides information about the project.

Coordinator
KAROLINSKA INSTITUTET 

Organization address
address: Nobels Vag 5
city: STOCKHOLM
postcode: 17177
website: www.ki.se

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 Sweden [SE]
 Total cost 191˙852 €
 EC max contribution 191˙852 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2020
 Duration (year-month-day) from 2020-07-01   to  2022-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KAROLINSKA INSTITUTET SE (STOCKHOLM) coordinator 191˙852.00

Map

 Project objective

'Cancer remains a leading cause of death worldwide, urging for innovative therapies. Infusion of natural killer (NK) cells, which possess an intrinsic capacity to eliminate cancer cells, is a promising treatment option for various tumours. Genetic engineering of NK cells before transfer allows to specifically tailor and modulate their anti-tumour responses. One particularly attractive strategy for broad implementation of NK cell immunotherapy in an “off-the-shelf” setting is to expand large numbers of NK cells from induced pluripotent stem cells (iPSCs). However, this approach is limited by two main bottlenecks: i) poor persistence of allogeneic iPSC-derived NK (iNK) cells due to rejection by the recipient immune system and ii) impaired functionality due to failure to achieve complete differentiation in vitro. The SYNKIT project seeks to address both of these current limitations through genetic engineering of iNK cells for increased persistence and function. Deletion of human leukocyte antigen (HLA) 'self-ligands' allows the transferred cells to escape from host T cells. However, absence of HLA also triggers “missing-self” recognition and rejection by host NK cells. In addition, new insights from the host laboratory into the molecular mechanism underlying NK cell education have unravelled a pathway of functional disarming in NK cells that lack self-ligands, further diminishing the anti-tumour efficacy of HLA-deficient NK cells. In SYNKIT, I will use HLA-deficient iNK cells as a platform to assess how introduction of synthetic self-ligands modulates the allogenicity and functionality of iNK cells. The overall goal of SYNKIT is to identify synthetic self-ligands, which reduce recognition by the host immune system and yet prevent functional disarming of the engineered iNK cells, thereby resulting in optimised anti-tumour function. Successful completion of SYNKIT will pave the way for development of next generation immunotherapy to more effectively combat cancer. '

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

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

IPG_CORE (2019)

Looking for the Impersonal Core -- Impersonal Pronouns across Germanic languages

Read More  

DIE_CKD (2019)

Deciphering intrarenal communication to unvail mechanisms of chronic kidney diseases

Read More  

THE CROSSMODAL BRAIN (2020)

Neural mechanisms of crossmodal activity in blind and sighted individuals

Read More