Purpose: T lymphocyte activation regulates the autocrine type secretio
n of interleukin-2, a T cell growth factor and the de novo expression
of its cell-surface receptor (IL-2R). Afterwards, a special, truncated
form of the IL-2R is secreted into the serum as a soluble molecule. S
oluble interleukin-2 receptor (sIL-2R) in serum is a non-specific mark
er of common activation of the cellular immune regulation. This study
reports the results of an early diagnostic observation of sIL-2R level
in the sera of 18 primary solid pediatric malignancies. Patients and
Methods: 18 children between the ages of 1 and 12 represented the Stud
y Group of solid tumor bearing patients. 12 healthy children between t
he ages of 1 and 12 represented the Control group. Concentrations of s
IL-2R were detected in the sera of the children employing a double-ant
ibody sandwich enzyme-linked immunosorbent assay (T Cell Sciences). Re
sults: Control Group concentrations of sIL-2R were in the range of 101
.9 to 255.3 IU/mL with a mean value of 178.6 IU/mL. Serum levels of sI
L-2R were markedly elevated in the sera of children with solid tumors
(Study Group) to levels between 223.8 IU/mL and 927 IU/mL with a mean
value of 575.4 IU/mL. Conclusions: 1) The shedding of cell-surface rec
eptors of immunological effector cells is a common physiological mecha
nism, 2) Presence of sIL-2R represents a sign of an overall activation
of the effector elements of the host's cellular immune system; 3) An
increase in the levels of sIL-2R represents an active phase of progres
sion; conversely, decreasing levels indicate tumor regression; 4) Seru
m levels of sIL-2Rs may represent a useful laboratory parameter in cho
osing an efficient anti-cancer therapy. Thus, the level of sIL-2R in c
hildhood solid tumor patients has a prognostic significance.