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IMMCEPTION SIGNED

Nociception and sensory nerves as regulators of type 2 immunity and skin inflammation

Total Cost €

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EC-Contrib. €

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Partnership

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 IMMCEPTION project word cloud

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

mast    informative    france    mas    interactions    delicate    mouse    innervated    allergic    imaging    evidences    performing    genetic    depends    model    molecules    meshwork    intravital    parallel    gaps    neuropeptide    tissue    gene    cord    suggested    equilibrium    human    immunological    resident    despite    homeostasis    analyzes    neuro    immunity    skin    spinal    dermatitis    environment    pathological    substance    nociceptors    perhaps    potentially    expression    transmission    pathophysiology    dermal    corresponding    therapeutic    organ    hypotheses    sensation    powerful    stimuli    preliminary    immune    sophisticated    discovered    solidly    macrophages    injurious    ongoing    patients    similarities    coupled    disorder    herein    lesional    protein    roles    signals    transmitting    relevance    translational    brain    b2    innovative    clinically    dysregulation    usa    nociception    sensory    wish    dendritic    nerves    inflammation    damaging    data    atopic    cells    mrgprb2    preserving    regulators    contributes    vivo    body    receptor    ad    structural    models    expressing    disorders    goals    cationic    harboring   

Project "IMMCEPTION" data sheet

The following table provides information about the project.

Coordinator
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE 

Organization address
address: RUE DE TOLBIAC 101
city: PARIS
postcode: 75654
website: www.inserm.fr

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 France [FR]
 Total cost 1˙497˙441 €
 EC max contribution 1˙497˙441 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2023-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE FR (PARIS) coordinator 1˙497˙441.00

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 Project objective

Preserving skin homeostasis depends on complex interactions among structural cells, immune cells, and the environment. Dysregulation of this delicate equilibrium contributes to the development of type 2 immunity-associated skin inflammation (i.e., allergic skin inflammation), including atopic dermatitis (AD). The skin is a complex organ harboring various tissue-resident immune cells (e.g., dendritic cells, mast cells and macrophages) and innervated by a meshwork of sensory nerves, including those involved in nociception (i.e., nociceptors), which respond to injurious or potentially damaging stimuli by transmitting signals to the spinal cord and brain. Despite their role in the transmission of sensation, recent evidences have suggested that nociceptors could be powerful regulators of ongoing immune response.

We wish to use sophisticated mouse models and new in vivo imaging approaches to define the roles of subsets of dermal nociceptors, cationic neuropeptide substance P, dermal mast cells expressing the recently discovered receptor for cationic molecules Mas-related G protein-coupled receptor b2 (i.e., Mrgprb2), in a mouse model of AD that has many pathological, immunological, and gene expression similarities with the corresponding human disorder. We also will define the translational relevance of our mouse studies by performing parallel analyzes of nociceptors and mast cells in the lesional skin of patients from USA and France with clinically-established AD. To accomplish these goals, we have proposed herein a body of work that is solidly based on our preliminary data, with four Aims that will test innovative hypotheses by using informative genetic approaches, as well as new intravital imaging systems we recently developed.

This work thus will address significant gaps in our knowledge about the pathophysiology of AD and has the potential to identify such neuro-immune interactions as a promising new therapeutic target in AD and perhaps other allergic disorders.

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

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