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#4980 : Investigate the regulation of IL-23R expression in innate and adaptive T cell populations
Topics: Epigenetics (ATAC-Seq)
Origin: IP
Project type: Development

Name of Applicant: YAHIA Hanane
Date of application: 25-01-2021
Unit: Immunoregulation
Location: 65-05-22
Phone: 3230
@ Mail: hanane.yahia@pasteur.fr
@ PI-Mail: lars.rogge@pasteur.fr

Project context and summary:

Chronic inflammatory diseases (CID) are clinically heterogeneous conditions that share common inflammatory pathways and derive from aberrant immune responses. Genome-wide association studies (GWAS), together with mouse models of autoimmune disease, demonstrated the implication of the IL-23 cytokine pathway in several CID. The overall goal of our work is to improve our understanding of the role of IL-23 in the pathophysiology of CIDs, such as axial spondyloarthritis, psoriatic arthritis, and psoriasis.


Related team publications:
S. Menegatti, V. Guillemot, E. Latis, H. Yahia-Cherbal, D. Mittermüller, V. Rouilly, E. Mascia, N. Rosine, S. Koturan, G. A. Millot, C. Leloup, D. Duffy, A. Gleizes, S. Hacein-Bey-Abina, Milieu Interieur Consortium, J. Sellam, F. Berenbaum, C. Miceli-Richard, M. Dougados, E. Bianchi, L. Rogge. Ann Rheum Dis, Epub ahead of print. doi: 10.1136/annrheumdis-2020-218304 (2020).
Yahia-Cherbal, H, Rybczynska M, Lovecchio D, Stephan T, Lescoat C, Placek K, Larghero J, Rogge L, Bianchi E* NFAT primes the human RORC locus for RORt expression in CD4+ T cells Nature Communications, 2019;10(1):4698.
Bianchi E, Rogge L. The IL-23/IL-17 pathway in human chronic inflammatory diseases-new insight from genetics and targeted therapies. Genes Immun. 2019 May;20(5):415-425. doi: 10.1038/s41435-019-0067-y.
Service Delivery
Manager: valerie.briolat@pasteur.fr
Status: Closed


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