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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.

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

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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