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.

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

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.)

HSQG (2020)

Higher Spin Quantum Gravity: Lagrangian Formulations for Higher Spin Gravity and Their Applications

Read More  

NSTree (2020)

Understanding substrate delivery for cell wall biosynthesis in plants

Read More  

RipGEESE (2020)

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

Read More