Abstract

We have investigated the serum concentrations of interleukin-6 (IL-6) and two IL-6 family cytokines-oncostatin M (OSM) and leukemia inhibitory factor (LIF)-in 63 patients with B-cell chronic lymphocytic leukemia (B-CLL) and 17 healthy controls using the enzyme-linked immunosorbent assay (ELISA) method. Simultaneously, we measured the serum levels of the soluble forms of two subunits of the IL-6 receptor complex-ligand binding glycoprotein 80 (sIL-6R) and glycoprotein 130 (sgp130). The cytokines and receptors were evaluated in 25 untreated patients and 38 patients treated with cladribine (2-CdA), as well as in 17 healthy controls. We have correlated the serum levels of these proteins with Rai's clinical stage of the disease, the response to 2-CdA treatment and some hematological parameters. We have also evaluated the correlation of the IL-6 serum level with the concentration of OSM and IL-6 soluble receptors. IL-6 was measurable in 62/63 (98.4%), OSM in 20/25 (80%) of untreated and 14/38 (37.8%) of the treated patients. sIL-6R and sgp130 were detectable in all 63 patients and LIF in none of the CLL patients. IL-6 serum level in untreated patients was not significantly different as compared to its concentration in the control group (P>0.05). However, in the patients treated with 2-CdA the IL-6 level was significantly lower (P<0.02), and the lowest concentration was found in the patients with complete remission (CR; median 1.4pg/ml; P<0.02). The concentration of sIL-6R was significantly higher in untreated (median 61.8 ng/ml) and treated (median 50.1 ng/ml) CLL patients when compared to normal persons (median 41.2 ng/ml; P=0.04; P<0.001, respectively). There was no difference between the sIL-6R levels in the patients with CR and the healthy controls. In non-responders sIL-6R concentration was the highest and similar to its level in the untreated patients. OSM level was higher in the untreated patients (median 1.8pg/ml) than in the normal controls (median 0.0pg/ml; P<0.001) and in the CR patients (median 0.0pg/ml; P<0.03). The serum concentration of sgp130 was similar in the untreated (median 480 pg/ml) and treated (median 470 pg/ml) patients, as well as in the healthy persons (median 420 pg/ml; P>0.05). We have found significant positive correlation between the levels of sIL-6R and the lymphocytes count in CLL patients (p=0.423; P<0.001). In addition, sIL-6R and OSM serum concentrations correlated also with CLL Rai stage. In conclusion, the serum level of IL-6, OSM and sIL-6R, but not LIF and sgp130, are useful indicators of CLL activity.

Highlights

  • inte rleukin-6 (IL-6) is of spec ial inte re st in B-chronic lymphocytic leukemia (CLL), be c ause this cytokine acts as a B-c ell stimulatory factor (BSF-II), mediates B-ce ll diffe re ntiation and can stimulate the grow th of B-c ell lymphoid malignanc ie s such as myeloma.[10]

  • Be cause le ukemia inhibitory fac tor (LIF) w as not detectable in any of the CLL patie nts, as w ell as in any person from the c ontrol group, w e did not carry out any statistical analysis for this cytokine

  • The re sults of some studies indic ate that IL-6 may play a role in the pathomechanism of CLL.[9,12]

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Summary

Introduction

B-cell chronic lymphocytic leukemia (CLL) is the most common le uke mia in the We ste rn w orld, charac te rize d by the clonal prolife ration and ac cumulation of B lymphocytes.[1,2] These leukemic lymphocytes are charac te rize d by the ex pre ssion of CD5 marker and low de nsity monoclonal membrane immunoglobulin (Ig). IL-6 related cytokines have a gp[130] rec eptor compone nt involve d in the signal transduc tion across the c ell me mbrane , w hich ex plains the func tional pleiotropy and re dundancy of IL-6 type c ytokine s.16. The ce llular IL-6 re ce ptor complex c onsists of tw o different prote ins [an 80-kDa ligand binding glyc oprote in (IL-6R) and gp 130] and is involved in c ellular signal transduc tion.[17,18] These tw o subunits of the IL6R c omplex are proteolytically cleave d and release d from the c ell as soluble re c eptor prote ins.[19,20] Soluble forms of the IL-6R (sIL-6R) and gp[130] (sgp130) have bee n found in diffe re nt body fluids in patients w ith various inflammatory and ne oplastic disease s.21,22. We have e valuate d the correlation be tw ee n the serum le vels of IL-6 w ith both OSM and IL-6 soluble rec eptors

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