The intercellular adhesion molecule 1 (ICAM-1) is the ligand for the l
ymphocyte function-associated antigen 1 (LFA-1). The ICAM-1/LFA-1 comp
lex mediates cell-cell and cell-matrix interactions and is believed to
be crucial for several immunological functions, including non-MHC-res
tricted cytoxicity. Recently, a circulating form of the surface ICAM-1
molecule, the 82 kDa cICAM, has been identified. Using enzyme-linked
immunosorbent assay (ELISA) we have examined 82 kDa cICAM-1 levels in
the sera of 45 age- and sex-matched healthy subjects and 130 consecuti
ve patients with Hodgkin's disease (HD). The mean +/- SD concentration
of the 82 kDa cICAM-1 was significantly higher (p < 0.001) in HD pati
ents (725.6 +/- 141 ng/ml) than in healthy controls (403.5 +/- 54.5 ng
/ml). Patients with B-symptoms (n = 66) had higher cICAM-1 levels than
patients without systemic symptoms (n = 64) (825.1 +/- 202.9 ng/ml ve
rsus 671.7 +/- 164.9 ng/ml; p < 0.001). Serum levels of cICAM-1 were a
lso significantly higher (p < 0.05) in patients with disseminated dise
ase (stage III and IV) than in those with localized disease (stage I a
nd II). The HD patients in stage III and IV with B-symptoms had signif
icantly higher (p < 0.001 and p < 0.02, respectively) cICAM-1 levels t
hen stage III/IV patients lacking B-symptoms. The increase of cICAM-1
concentrations was positively correlated to increases of soluble recep
tors for interleukin-2 (sIL-2R) (r = 0.69; p < 0.001). Since cICAM-1 i
s functionally able to bind to LFA-1, increased serum levels of this m
olecule could be a mechanism for promoting de-adhesion and inability o
f Hodgkin and Reed-Sternberg cells (H-RS) to be recognized by cytotoxi
c effector cells, and could thus represent a way for these cells to es
cape immunosurveillance and for progression and spreading of disease.