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SkinTrmDeep SIGNED

Tissue Resident Memory (Trm) CD8+ T cells: Genome-wide dissection of cellular differentiation and heterogeneity

Total Cost €

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EC-Contrib. €

0

Partnership

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 SkinTrmDeep project word cloud

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

lymphocytes    epigenetic    immunity    populations    cd8    mounting    framework    host    generating    basis    genome    effector    biology    immunotherapies    integral    mechanisms    pathology    heterogeneity    promise    single    function    lymphoid    skin    denominators    patient    rna    decipher    functionally    independent    lymphocyte    diverse    trm    cytotoxic    cytokine    flow    barrier    young    unprecedented    population    microenvironment    tissues    determined    encompassing    chromatin    ultimate    career    molecular    resolution    eliciting    illuminate    profiles    collaborations    capacity    gut    poorly    am    immune    memory    cytometry    sorting    lungs    limited    pathogens    samples    differentiation    map    shaping    functions    residency    cell    throughput    transcription    localized    binding    identification    cells    critical    coupled    tissue    phenotypically    cellular    human    resident    circulating    potentially    comprising    unravelling    accessibility    protection    sequencing    regulatory    forefront    ontogeny    rely    goals    interactions    surfaces    organs    producing    predominant    understand    imprinting    unravel    scientist    multidisciplinary    diseases   

Project "SkinTrmDeep" 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 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-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-03-01   to  2021-02-28

 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

Tissue-resident memory (Trm) cells are non-circulating T lymphocytes of non-lymphoid tissues and organs that provide localized protection at barrier surfaces such as skin, gut and lungs. In human skin, Trm cells represent the predominant lymphocyte population, comprising subsets with different cytokine profiles and cytotoxic capacity. They represent an integral part of barrier immunity, mounting tailored responses to diverse pathogens, but potentially also eliciting immune pathology. Trm cell differentiation, effector mechanisms and cellular interactions remain poorly defined. I aim to decipher cytotoxic Trm cell biology in greater depth, unravelling the epigenetic framework of phenotypically and functionally distinct CD8 Trm populations. I will rely on state-of-the-art methodologies at the host institution. Through unique collaborations and a multidisciplinary approach encompassing advanced flow cytometry, cell sorting and high-throughput sequencing, I propose to map genome-wide chromatin accessibility in skin and gut Trm cell subsets. Identification of regulatory elements critical for cell functions coupled with analyses of transcription factor binding promise to unravel the molecular mechanisms defining Trm cell ontogeny, function and tissue-specific imprinting. Moreover, with potential application to limited patient samples, single-cell RNA sequencing of cytokine-producing cells will provide a map of Trm cell heterogeneity with unprecedented resolution. This project will illuminate the role of the microenvironment in shaping tissue-resident memory, with ultimate goals to understand Trm cell-related diseases and determine common denominators required to establish tissue residency and provide basis for generating and shaping Trm cells in future cellular immunotherapies. Being at the forefront of the research on the epigenetic differentiation processes of lymphocytes, I am determined to build a strong basis for a future career as a young independent scientist.

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

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