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Author
- Seneschal, Julien2
- Taieb, Alain2
- Bertolotti, Antoine1
- Boukhedouni, Nesrine1
- Darrigade, Anne-Sophie1
- Das, Soumen1
- Dessarthe, Benoît1
- Ezzedine, Khaled1
- Grasseau, Alexis1
- Han, Xianlin1
- Jacquemin, Clément1
- Lee, Bongyong1
- Lucchese, Fabienne1
- Martins, Christina1
- Perera, Ranjan J1
- Rambert, Jérôme1
- Sahoo, Anupama1
- Sahoo, Sanjaya K1
- Seal, Sudipta1
- Seki, Tatsuya1
- Steppie, Michael1
- Thiolat, Denis1
- Vernisse, Charlotte1
- Wang, Chunyan1
Melanoma
2 Results
- Original Article Immunology/InfectionOpen Archive
Vitiligo Skin Is Imprinted with Resident Memory CD8 T Cells Expressing CXCR3
Journal of Investigative DermatologyVol. 138Issue 2p355–364Published online: September 16, 2017- Katia Boniface
- Clément Jacquemin
- Anne-Sophie Darrigade
- Benoît Dessarthe
- Christina Martins
- Nesrine Boukhedouni
- and others
Cited in Scopus: 134Vitiligo is a chronic autoimmune depigmenting skin disorder that results from a loss of melanocytes. Multiple combinatorial factors have been involved in disease development, with a prominent role of the immune system, in particular T cells. After repigmentation, vitiligo frequently recurs in the same area, suggesting that vitiligo could involve the presence of resident memory T cells (TRM). We sought to perform a thorough characterization of the phenotype and function of skin memory T cells in vitiligo. - Original Article Melanocytes/MelanomaOpen Archive
MicroRNA-211 Regulates Oxidative Phosphorylation and Energy Metabolism in Human Vitiligo
Journal of Investigative DermatologyVol. 137Issue 9p1965–1974Published online: May 11, 2017- Anupama Sahoo
- Bongyong Lee
- Katia Boniface
- Julien Seneschal
- Sanjaya K. Sahoo
- Tatsuya Seki
- and others
Cited in Scopus: 50Vitiligo is a common chronic skin disorder characterized by loss of epidermal melanocytes and progressive depigmentation. Vitiligo has complex immune, genetic, environmental, and biochemical causes, but the exact molecular mechanisms of vitiligo development and progression, particularly those related to metabolic control, are poorly understood. In this study we characterized the human vitiligo cell line PIG3V and the normal human melanocyte line HEM-l by RNA sequencing, targeted metabolomics, and shotgun lipidomics.