Hc. Kluinnelemans et al., PROLIFERATION AND CYTOGENETIC ANALYSIS OF HAIRY-CELL LEUKEMIA UPON STIMULATION VIA THE CD40 ANTIGEN, Blood, 84(9), 1994, pp. 3134-3141
Using the CD40 system, in vitro proliferation of hairy cell leukemia (
HCL) was examined in 43 patients. In this culture system, cells were s
timulated by interleukin-4 (IL-4) and anti-CD40 monoclonal antibodies
(MoAbs) that were added in soluble form or were cross-linked via their
Fc part using Fc gamma RII-transfected mouse fibroblast cells. prolif
eration was induced and confirmed by H-3-thymidine incorporation in 14
cases and by the presence of metaphases in 42 cases. H-3-thymidine in
corporation showed a heterogeneous pattern: cross-linking of anti-CD40
gave the highest proliferation in 8 cases; in 11 cases. stimulation w
ith anti-CD40 MoAbs alone, without cross-linking also resulted in prol
iferation; the addition of IL-4 further enhanced H-3-thymidine incorpo
ration in 5 cases, but suppressed this phenomenon in 5 other cases. Th
e CD40 system proved to be very effective in obtaining cytogenetic dat
a. With a success rate of 42 of 43 patients tested, we found clonal ab
normalities in 8 cases (19%) and nonclonal abnormalities with involvem
ent of one or two abnormal metaphases in another 7 cases. The chromoso
mes most frequently involved in the abnormal karyotypes, both structur
ally and numerically, were chromosomes 5, 7, and 14. By fluorescence-a
ctivated cell-sorting analysis of the cultured cells, and by immunophe
notypic analysis of metaphase spreads, T-cell growth could be excluded
and the HCL-lineage confirmed. Stimulation via the CD40 antigen is an
excellent tool for growing hairy cell leukemia cells. (C) 1994 by The
American Society of Hematology.