Publication | Open Access
T- and b-lymphocytes and lymphoblasts in untreated acute lymphocytic leukemia
62
Citations
28
References
1974
Year
Hematological MalignancyLymphoid NeoplasiaAllergyAutoimmune DiseaseMain SubpopulationsMixed-phenotype Acute LeukemiaMalignant Blood DisorderHematologyImmunologyPathologyBone MarrowAutoimmunityBone Marrow BlastsAdult T-cell Leukemia-lymphomaImmunotherapyMedicine
This study demonstrates in the peripheral blood and bone marrow of patients with untreated acute lymphocytic leukemia (ALL) the coexistence of two main subpopulations of lymphoid cells: 1) small lymphoid cells which bear the same surface markers as normal lymphocytes; and 2) blasts which in the majority of the patients lack these markers. The proportions of cells bearing different cell-surface markers were studied in 14 children with ALL at time of diagnosis. Thymus-dependent (T) cells were identified by spontaneous formation of rosettes with sheep erythrocytes, and thymus-independent (B) cells by immunofluorescence of surface immunoglobulins. Using these criteria we demonstrated small lymphocytes with T- or B-markers in the peripheral blood or bone marrow of all patients assayed. In contrast, in 10 of 14 children the blasts had no detectable markers. However, in 2 patients more than half of bone marrow blasts had T-cell surface receptors, and in another 2 the proportion of blasts forming rosettes was 2% and 17%. The initial blast cell count in peripheral blood was greater than 105/mm3 in both children with the higher proportion of T-lymphoblasts. An additional initial clininal feature in one of them was the presence of a large anterior mediastinal mass, probably thymus. After successful induction of remission there was an increase in the proportion of normal T-lymphocytes in the bone marrow of 9 children assayed. The results from this study suggest that the presence of T-lymphoblasts, which may be of thymic origin, is correlated with a more advanced disease at time of diagnosis.
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