Objective. Determine the molecular defects underlying the CD3(-)CD4(+) T-cell phenotype and persistence of this clonal population in patients with hypereosinophilic syndrome. Patients and Methods. Patients in this study suffer from the lymphocytic variant of hypereosinophilic syndrome distinguished by a CD3(-)CD4(+) T-cell clone that overexpresses Th2 cytokines upon activation and thereby provokes the eosinophilia. Interleukin-2-dependent CD3(-)CD4(+) T-cell lines were derived from patient blood at various disease stages and used to investigate the molecular modifications correlated with their abnormal phenotype. Results. We demonstrate that the CD3(-)CD4(+) T cells, characterized by a clonal TCR beta gene rearrangement, maintained the same immunophenotype over the 6-year period of our study, during which one patient progressed from premalignant disease to CD3(-)CD4(+) T-cell lymphoma. We show that a specific loss of CD3 gamma gene transcripts is responsible for the defect in TCR/CD3 surface expression. In addition, the level of NFATc2 binding to NFAT motifs in the CD3 gamma gene promoter was greatly increased in the abnormal T cells. Our studies indicate that CD3 gamma promoter activity can be positively influenced by NFATc1 plus NF-kappa B p50 and negatively regulated by NFATc2 containing complexes. We show that in patients' CD3(-)CD4(+) T cells, an increase in nuclear NFATc2 occurs in parallel with a decrease in NFATc1 and NF-kappa B gene expression. Conclusion. Hypereosinophilic syndrome joins the growing number of pathological conditions where a defect in surface expression and/or function of the TCR/CD3 complex results from altered regulation of CD3 gamma gene expression. (c) 2005 International Society for Experimental Hematology.
Willard-Gallo, K., Sibille, C., Badran, B., Ravoet, M., Zerghe, A., Burny, A., Martiat, P., Goldman, M., & Roufosse, F. (2005). Defective CD3 gamma gene transcription is associated with NFATc2 overexpression in the lymphocytic variant of hypereosinophilic syndrome. Experimental Hematology, 33(10), 1147-1159. https://doi.org/10.1016/j.exphem.2005.06.027 (Original work published 2005)