TCRγδ+ large granular lymphocyte leukemias reflect the spectrum of normal antigen-selected TCRγδ+ T-cells
Autor: | Anthonie Willem Langerak, Ana Balanzategui, Margarida Lima, J. J. M. Van Dongen, Julia Almeida, Marcos González, Henk Wind, Paloma Bárcena, A. Orfao, E. J. Van Gastel-Mol, Tomasz Szczepański, J F San Miguel, Yorick Sandberg |
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Rok vydání: | 2006 |
Předmět: |
Cancer Research
Pathology medicine.medical_specialty business.industry T cell CD11c chemical and pharmacologic phenomena Hematology Gene rearrangement medicine.disease Pancytopenia Leukemia Immunophenotyping medicine.anatomical_structure Oncology hemic and lymphatic diseases Immunology medicine CD5 business T-Cell Large Granular Lymphocyte Leukemia |
Zdroj: | Digital.CSIC. Repositorio Institucional del CSIC instname |
Popis: | T-cell large granular lymphocytes (LGL) proliferations range from reactive expansions of activated T cells to T-cell leukemias and show variable clinical presentation and disease course. The vast majority of T-LGL proliferations express TCRαβ. Much less is known about the characteristics and pathogenesis of TCRγδ+ cases. We evaluated 44 patients with clonal TCRγδ+ T-LGL proliferations with respect to clinical data, immunophenotype and TCR gene rearrangement pattern. TCRγδ+ T-LGL leukemia patients had similar clinical presentations as TCRγδ+ T-LGL leukemia patients. Their course was indolent and 61% of patients were symptomatic. The most common clinical manifestations were chronic cytopenias - neutropenia (48%), anemia (23%), thrombocytopenia (9%), pancytopenia (2%) - and to a lesser extent splenomegaly (18%). Also multiple associated autoimmune (34%) and hematological (14%) disorders were found. Leukemic LGLs were predominantly positive for CD2, CD5, CD7, CD8, and CD57, whereas variable expression was seen for CD16, CD56, CD11b, and CD11c. The Vγ9/Vδ2 immunophenotype was found in 48% of cases and 43% of cases was positive for Vδ1, reflecting the TCR-spectrum of normal TCRγδ+ T-cells in adult PB. Identification of the well-defined post-thymic Vδ2-Jδ1 selection determinant in all evaluable Vγ9+Nδ2+ patients, is suggestive of common (super)antigen involvement in the pathogenesis of these TCRγδ+ T-LGL leukemia patients. © 2006 Nature Publishing Group All rights reserved. This study has been supported by a grant from the Dutch Cancer Society (to YS) and partially supported by the following grants: Fondo de Investigación Sanitaria, Ministerio de Sanidad y Consumo, Madrid, Spain (grant FIS 02/1244), the Consejería de Educación y Cultura, Junta de Castilla y León, Valladolid, Spain (grant SA 103/03) and the University of Salamanca, Salamanca, Spain (Ref. No. 430 to PB). |
Databáze: | OpenAIRE |
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