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TCRabX SIGNED

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

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 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.

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

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.

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The information about "TCRABX" are provided by the European Opendata Portal: CORDIS opendata.

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