MALIGNANT B-CELL CD5 MEMBRANE PHENOTYPE AND B-CELL COLONY GROWTH IN-VIVO AND IN-VITRO IN PATIENTS WITH B-CHRONIC LYMPHOCYTIC-LEUKEMIA - ANALYSIS WITH CLINICAL-PARAMETERS
I. Hings et al., MALIGNANT B-CELL CD5 MEMBRANE PHENOTYPE AND B-CELL COLONY GROWTH IN-VIVO AND IN-VITRO IN PATIENTS WITH B-CHRONIC LYMPHOCYTIC-LEUKEMIA - ANALYSIS WITH CLINICAL-PARAMETERS, Leukemia & lymphoma, 12(1-2), 1993, pp. 59-67
Chronic lymphocytic leukemia (CLL), despite an overall good prognosis,
has a subgroup of patients with more rapid, aggressive disease. In an
attempt to generate additional information about the B cell clones in
B-CLL which could be used as predictive parameters, we analysed CD5 m
embrane phenotype and B cell colony growth in 29 B-CLL patients. CD5,
a 67-kd glycoprotein, has been reported to be a consistent feature of
the malignant B cell membrane phenotype in CLL. We used an in vitro B
cell colony assay to study the in vitro growth, differentiation, and c
ell surface properties of CLL B cells, Finally, a variety of standard
clinical parameters were collated for each patient. Monoclonal antibod
ies to both CD5 and CD19 (pan B cell marker) were used to perform 2-co
lor flow cytometry on freshly purified CLL B cells and on CLL B cells
harvested after 7 days of in vitro culture. We demonstrate here that C
LL B cells are heterogeneous with respect to their expression of CD5,
and that this expression is not fixed but may vary both in vivo and in
vitro. In vitro growth potential, as measured by the B cell colony as
say, was also heterogeneous with three subgroups defined as low growth
(<10 colonies), intermediate (10-100 colonies) and high growth (>100
colonies). Furthermore a T cell conditioned medium was not found to be
a requirement for in vitro colony growth in the majority of CLL B cel
ls. In addition, we evaluated the potential correlation of B cell CD5
phenotype or B cell colony growth on standard clinical parameters. A c
orrelation between high CD5 expression (>85% CD5 positive) and lymphoc
yte doubling time less than 12 months and treatment within six months
was detected. This study emphasizes that additional information regard
ing the biology of the malignant CLL B cell will generate new paramete
rs that can be used to help predict the clinical course of B-CLL.