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MIRA

Characterizing Microbe-specific Immune Responses in the pathogenesis of Autoimmunity

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 MIRA project word cloud

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

mice    patients    plasticity    fail    regionalization    helper    anatomically    dysregulation    mechanisms    techniques    commensal    events    context    unmet    function    exposed    susceptibility    medical    ibd    incidence    dysregulated    mucosal    form    foremost    populations    shape    microbial    localized    immunodominant    recognize    cd4    rna    homing    antigens    functions    chronic    luminal    microbiota    generation    localization    differential    transgenic    treatment    pivotal    cutting    sequencing    antigen    worldwide    pathogenesis    adaptive    therapy    bowel    disease    severity    heterogeneity    inflammation    cells    population    alter    inflammatory    single    tcr    diversity    immune    dramatically    immunological    regions    immunotherapies    vivo    differentiation    forms    points    characterization    determines    intestines    comprise    diseases    cbir1    anatomical    deeply    gut    proportion    little    underlying    combine    therapeutic    cell    balance    edge    severely    intestinal   

Project "MIRA" 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]
 Project website https://villablancalab.com/
 Total cost 173˙857 €
 EC max contribution 173˙857 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2016
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2017
 Duration (year-month-day) from 2017-09-01   to  2019-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KAROLINSKA INSTITUTET SE (STOCKHOLM) coordinator 173˙857.00

Map

 Project objective

Dysregulation in the balance of CD4 T helper cell populations can severely alter susceptibility to a number of chronic inflammatory diseases, including inflammatory bowel disease (IBD). The incidence of IBD is dramatically increasing in Europe and worldwide and its therapy represents an important unmet medical need, since a significant proportion of patients fail to respond to currently available immunotherapies. Therefore, a better characterization of the immunological events underlying each form of IBD is of foremost importance. Increasing evidence points to the pivotal role of a dysregulated mucosal immune response to the intestinal microbiota in the pathogenesis of IBD. However, little is known about the mechanisms contributing to the generation of commensal-specific adaptive immune responses, and whether their differential localization can shape severity and anatomical extent of the disease. Indeed, the intestines comprise anatomically distinct regions that are exposed to different luminal antigens and this diversity eventually determines a regionalization of intestinal immune functions and microbiota-specific T cell responses. The aim of this proposal is to deeply characterize microbiota-specific T cell responses generated under different inflammatory conditions, in terms of differentiation, plasticity, heterogeneity, function and homing potential. To this aim, the proposed work will combine the use of CBir1 TCR transgenic mice, whose T cells recognize a microbial antigen that is immunodominant in IBD patients, and cutting-edge techniques such as single-cell RNA sequencing. By modelling the microbiota-specific immune response in vivo in the context of gut inflammation, I will characterize the function and homing properties of microbiota-specific T cells at the population and single-cell level, aiming at identifying new therapeutic targets for the treatment of localized forms of gut inflammation.

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

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