Opendata, web and dolomites

TCRabX SIGNED

Structural basis for the therapeutic efficiency of optimal-affinity T cell receptors

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 TCRabX project word cloud

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

identification    mice    hugely    regression    cognate    cell    dimensional    population    immunotherapy    chemotherapy    repertoire    form    tumour    immunology    berlin    structural    therapeutic    complementarity    citizens    peripheral    receptor    begin    13    tool    therapeutically    gene    australia    pmhc    mhc    crystallography    demographic    self    cancer    surgery    peptide    elderly    genes    helps    humanized    aged    molecules    made    types    clinical    alternative    patient    human    date    diverse    analysed    3d    alpha    chains    class    topologies    delay    health    trials    macromolecules    affinity    points    worldwide    tcrabx    melbourne    treatment    radiation    antigens    regions    negative    tcr    people    interdisciplinary    biological    blood    mediated    optimal    isolated    contact    complexed    innovative    middle    newly    structures    incidence    cdrs    connects    uncovered    rates    exceptional    specificity    benefit    beta    recognizing    biology    powerful    germany    ray    histocompatibility    docking    lymphocytes    biomedical    respectively    efficient    antigen    transfer    supporting    cells    naturally    loaded    determined    world    therapy    cdr    ageing    tcrs   

Project "TCRabX" data sheet

The following table provides information about the project.

Coordinator
CHARITE - UNIVERSITAETSMEDIZIN BERLIN 

Organization address
address: Chariteplatz 1
city: BERLIN
postcode: 10117
website: www.charite.de

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 Germany [DE]
 Total cost 264˙110 €
 EC max contribution 264˙110 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-GF
 Starting year 2019
 Duration (year-month-day) from 2019-08-01   to  2022-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CHARITE - UNIVERSITAETSMEDIZIN BERLIN DE (BERLIN) coordinator 264˙110.00
2    MONASH UNIVERSITY AU (VICTORIA) partner 0.00

Map

 Project objective

Demographic change includes population ageing, and incidence rates begin to increase for many types of cancer in middle-aged and elderly people. Traditional cancer treatment includes surgery, chemotherapy, and radiation therapy, while tumour immunotherapy by T cell receptor (TCR) gene transfer represents an alternative form of treatment. The transfer of tumour-specific TCR genes into patient’s peripheral blood lymphocytes targets cancer specifically and effectively. But while patient-derived low-affinity TCRs do not show therapeutic activity, optimal-affinity TCRs, as isolated from newly-generated antigen-negative humanized mice with a diverse human TCR repertoire, can effectively delay tumour regression. X-ray crystallography is a powerful tool of structural biology, which helps researchers to identify the three-dimensional (3D) structures of biological macromolecules such as TCRs complexed to their cognate peptide-loaded major histocompatibility complex (pMHC) molecules. Recent research uncovered the docking topologies of naturally selected TCRs, but therapeutically efficient optimal-affinity TCRs recognizing tumour-associated self-antigens, have not been analysed to date. The exceptional specificity of TCRs is determined by three complementarity-determining regions (CDRs) of the TCR alpha- and beta-chains. Biomedical research on TCR gene therapy and design of future clinical trials will hugely benefit from the identification of CDR-mediated contact points made between therapeutic TCRs and the pMHC on their target cells. TCRabX is an interdisciplinary research project investigating the 3D structures of 13 TCRs complexed to MHC-I or MHC-II, respectively. It connects innovative clinical immunology research in Berlin/Germany and world-class structural biology research in Melbourne/Australia. The proposed research will enhance the health and well-being of citizens in Europe and worldwide by supporting the advancement of cancer immunotherapy approaches.

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

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

EngPTC2 (2019)

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

Read More  

NSTree (2020)

Understanding substrate delivery for cell wall biosynthesis in plants

Read More  

MemoryAggregates (2020)

Mechanism of Whi3 Aggregation and its Age-dependent Malfunction

Read More