Explore the words cloud of the ILC_REACTIVITY project. It provides you a very rough idea of what is the project "ILC_REACTIVITY" about.
The following table provides information about the project.
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
|Coordinator Country||France [FR]|
|Total cost||1˙899˙375 €|
|EC max contribution||1˙899˙375 € (100%)|
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
|Duration (year-month-day)||from 2016-08-01 to 2021-07-31|
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|1||INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE||FR (PARIS)||coordinator||1˙899˙375.00|
Innate lymphoid cells (ILC) are a newly described family of hematopoietic cells that lack antigen-specific receptors but can be activated to promptly produce large amounts of cytokines (including interleukin (IL)-5, -13, -17A, -22, TNF-α and interferon-γ) and thereby contribute to the immediate, first-line immune defense against viral, bacterial, and parasitic infections. ILCs include the previously described natural killer (NK) cells and have a similar 'natural' effector function which is immediately available during immune responses and prior to that of adaptive immunity. Three groups of ILC (ILC1, ILC2, ILC3) have been described that share biological activities of T helper (Th)1, Th2 and Th17/22 subsets and CTL. ILCs are active during both fetal and adult life and play important roles in the homeostasis of mucosal and non-mucosal tissues. Nevertheless, how ILCs are integrated into ongoing immune responses remains unclear and this knowledge is a prerequisite for harnessing the clinical potential of these immune effector cells. This proposal will investigate critical checkpoints that can regulate ILC reactivity for immune responses in humans and mice. The four proposed objectives will be addressed using a combination of cutting-edge technologies including innovative mouse models that can report on ILC biology in vivo, single cell transcriptional and functional analysis of diverse circulating and tissue human and mouse ILC subsets, ‘digital’ pathogen-dependent ILC activation approaches and computational analysis of large immunological datasets from healthy, normal human individuals. Collectively, these complementary studies will shed new light on the biological determinants which condition ILC reactivity in humans and mice. Understanding how the threshold of ILC responsiveness is set prior to and during immune responses will have important implications for disease intervention.
|year||authors and title||journal||last update|
Pedro M. Rodrigues, Ana R. Ribeiro, Nicolas Serafini, Catarina Meireles, James P. Di Santo, Nuno L. Alves
Intrathymic Deletion of IL-7 Reveals a Contribution of the Bone Marrow to Thymic Rebound Induced by Androgen Blockade
published pages: 1389-1398, ISSN: 0022-1767, DOI: 10.4049/jimmunol.1701112
|The Journal of Immunology 200/4||2019-06-13|
Pedro GonÃ§alves, JoÃ£o Ricardo AraÃºjo, James P Di Santo
A Cross-Talk Between Microbiota-Derived Short-Chain Fatty Acids and the Host Mucosal Immune System Regulates Intestinal Homeostasis and Inflammatory Bowel Disease
published pages: 558-572, ISSN: 1078-0998, DOI: 10.1093/ibd/izx029
|Inflammatory Bowel Diseases 24/3||2019-06-13|
Wei Xu, Dylan E. Cherrier, Sylvestre Chea, Christian Vosshenrich, Nicolas Serafini, Maxime Petit, Pentao Liu, Rachel Golub, James P. Di Santo
An Id2RFP-Reporter Mouse Redefines Innate Lymphoid Cell Precursor Potentials
published pages: , ISSN: 1074-7613, DOI: 10.1016/j.immuni.2019.02.022
Dylan E. Cherrier, Nicolas Serafini, James P. Di Santo
Innate Lymphoid Cell Development: A T Cell Perspective
published pages: 1091-1103, ISSN: 1074-7613, DOI: 10.1016/j.immuni.2018.05.010
Eric Vivier, David Artis, Marco Colonna, Andreas Diefenbach, James P. Di Santo, GÃ©rard Eberl, Shigeo Koyasu, Richard M. Locksley, Andrew N.J. McKenzie, Reina E. Mebius, Fiona Powrie, Hergen Spits
Innate Lymphoid Cells: 10 Years On
published pages: 1054-1066, ISSN: 0092-8674, DOI: 10.1016/j.cell.2018.07.017
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