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Emergence of a STAT3 mutated NK clone in LGL leukemia.
Yan, Yiyi; Olson, Thomas L; Nyland, Susan B; Feith, David J; Loughran, Thomas P.
Afiliación
  • Yan Y; Department of Medicine, York Hospital, York, PA, USA.
  • Olson TL; University of Virginia Cancer Center, P.O. Box 800334, Charlottesville, VA 22908-0334, USA.
  • Nyland SB; University of Virginia Cancer Center, P.O. Box 800334, Charlottesville, VA 22908-0334, USA.
  • Feith DJ; University of Virginia Cancer Center, P.O. Box 800334, Charlottesville, VA 22908-0334, USA.
  • Loughran TP; University of Virginia Cancer Center, P.O. Box 800334, Charlottesville, VA 22908-0334, USA.
Leuk Res Rep ; 4(1): 4-7, 2015.
Article en En | MEDLINE | ID: mdl-25709890
Large granular lymphocyte (LGL) leukemia is a chronic clonal lymphoproliferative disorder. Here, a T-LGL leukemia patient developed NK-LGL leukemia with residual leukemic T-LGL. TCRVß usage and CDR3 sequence drifts were observed with disease progression. A STAT3 S614R mutation was identified in NK but not T-cells in the mixed leukemic stage. Multiple, non-dominant T-cell clones with distinct STAT3 mutations were present throughout. Our results suggest that T and NK-LGL leukemia may share common pathogenesis mechanisms and that STAT3 mutation alone is insufficient to bring about clonal expansion. Mutational and immunological monitoring may provide diagnostic and therapeutic significance in LGL leukemia.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Leuk Res Rep Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Leuk Res Rep Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos