Fiche publication
Date publication
janvier 2015
Journal
The Journal of investigative dermatology
Auteurs
Membres identifiés du Cancéropôle Est :
Pr BENSUSSAN Armand
Tous les auteurs :
Moins-Teisserenc H, Daubord M, Clave E, Douay C, Félix J, Marie-Cardine A, Ram-Wolff C, Maki G, Beldjord K, Homyrda L, Michel L, Bensussan A, Toubert A, Bagot M
Lien Pubmed
Résumé
The diverse aspects of cutaneous T-cell lymphomas may impede the diagnosis of Sézary syndrome (SS) and mycosis fungoides (MF), in particular, at early stages of the disease. We defined the CD158k/KIR3DL2 molecule as a first positive cell surface marker for Sézary cells (SCs). Here, we designed an optimized flow cytometry gating strategy, allowing the definition of lymphocytes of different sizes and defects of cell surface markers. Quantification by cytomorphology, flow cytometry, or clonal evaluation, gave similar results at initial time points and during the evolution in a prospective study involving 64 consecutive cutaneous T-cell lymphoma or erythrodermic patients. We found that CD158k+ T cells and circulating CD4+ T cells from MF patients exhibited unexpected patterns of cell surface expression with a marked heterogeneity of circulating lymphocytes even at initial diagnosis. Taken together, our results show that a multistep gating of CD158k+ cells is reliable to assess tumor burden in case of SS and suggest that both circulating MF CD4+ T cells and CD158k+ T cells are not homogeneous distinct memory populations. Further phenotypic and functional characterizations of such subsets are needed to better understand the underlying molecular mechanisms leading to the development of these diseases.
Mots clés
Aged, Aged, 80 and over, Antibodies, Monoclonal, immunology, Biomarkers, Tumor, immunology, Disease Progression, Follow-Up Studies, Genetic Heterogeneity, Humans, Immunologic Memory, Longitudinal Studies, Lymphocyte Subsets, metabolism, Lymphoma, T-Cell, Cutaneous, metabolism, Middle Aged, Mycosis Fungoides, metabolism, Neoplastic Cells, Circulating, metabolism, Prospective Studies, Receptors, KIR2DL2, immunology, Sezary Syndrome, diagnosis
Référence
J Invest Dermatol. 2015 01;135(1):247-257
