S. Molica et al., Clinico-biological implications of increased serum levels of interleukin-8in B-cell chronic lymphocytic leukemia, HAEMATOLOG, 84(3), 1999, pp. 208-211
Background and Objective. Constitutive cellular expression and serum releas
e of biologically active interleukins (IL-8) has been reported in B-cell ch
ronic lymphocytic leukemia (CLL). Given the autocrine role played by IL-8 i
n the process of cell accumulation characteristic of this disease we tried
to investigate clinico-biological implications of Increased serum levels of
this cytokine in an unselected series of B-cell CLL patients.
Design and Methods. Serum levels of IL-8 were determined at the time of dia
gnosis in 58 previously untreated B-CLL patients using an immunoenzyme assa
y. Results were correlated with main clinico-hematologic features as well a
s with the risk of disease progression. Finally, we looked for associations
between IL-8 and molecules directly involved in apoptosis, such as intrace
llular bcl-2 and soluble APO1/Fas.
Results. Increased serum levels of IL-8 were found in 15 out of 58 (25.8%)
B-cell CLL patients. Serum levels of IL-8 did not reflect clinico-biologica
l features representative of tumor mass such as clinical stage, histopathol
ogic pattern of bone marrow (BM) involvement, beta(2)-microglobulin, sCD23
and sCD27 titers. Interestingly, circulating levels of IL-8 paralleled thos
e of intracellular bcl-2 (r = 0.522; p = 0.01), thus confirming that the an
tiapoptotic effect of IL-8 can be exerted through a bcl-2 dependent pathway
. Levels of IL-8 did not match those of soluble Apo-1/Fas (r = -0.013; p =
0.943). Finally, stage A patients with levels of IL-8 above the median valu
e (i.e. 4.5 pg/mL) were more likely to progress to a more advanced clinical
stage than those with levels below the median value (p < 0.05).
Interpretation and Conclusions. IL-8 is an interesting marker in B-cell CLL
, closely involved in the pathogenesis of disease. Furthermore, it is usefu
l for predicting the pace of disease progression in early clinical stages.
(C) 1999, Ferrata Storti Foundation.