A highly malignant human T-cell leukemia was identified by cell surface analysis as a member of the T-cell receptor (TCR) γδ lineage. Cytogenetic and molecular analysis showed a novel t(8;14)(q24;q11) rearrangement involving the J(δ1) gene segment on chromosome 14 and the distal end of chromosome 8 near the c-myc proto-oncogene locus. The γδ TCR of the leukemia blasts was functionally intact and could be activated to generate intracellular calcium flux and to target Fc receptor-mediated redirected tumor cell lysis. In addition, non-major histocompatibility complex restricted lysis of a limited target cell panel was shown by fresh leukemic blasts and by the in vitro-maintained leukemia cells that was comparable to known T-cell lines with natural killer-like activity. These data suggest that the T-cell leukemia potentially had in vivo functional cytolytic activity. However, whether this activity did contribute to the patient's clinical condition could not be determined.
|Original language||English (US)|
|Number of pages||9|
|State||Published - 1992|
ASJC Scopus subject areas
- Cell Biology