Rc. Smallridge et al., SOLUBLE INTERLEUKIN-2 RECEPTOR IS A THYROID HORMONE-DEPENDENT EARLY-RESPONSE MARKER IN THE TREATMENT OF THYROTOXICOSIS, Clinical and diagnostic laboratory immunology, 4(5), 1997, pp. 583-586
Thyrotoxic patients exhibit increased levels of immune activation mole
cules (soluble interleukin-2 receptor [sIL-2R], intercellular adhesion
molecule-1 [ICAM-1], and endothelial-leukocyte adhesion molecule-1 [E
LAM-1]) in serum, although the clinical significance of these measurem
ents remains unclear, In a randomized ii-week study, we have recently
shown that in the treatment of hyperthyroidism, the combination of cho
lestyramine and methimazole (MMI) resulted in faster lowering of serum
thyroid-hormone levels than did MMI alone, Stored serial serum sample
s from patients participating in this randomized treatment trial were
analyzed for sIL-2R, soluble ICAM-1 (sICAM-1), and soluble ELAM-1 (sEL
AM-1), The levels of all three molecules were elevated in patients wit
h hyperthyroidism, Although the levels of sICAM-1 and sELAM-1 remained
elevated through the 4-week follow-up period in both groups of patien
ts, the sIL-2R levels (normal levels, 1.0 to 4.2 ng/ml) decreased sign
ificantly in the 10 patients who received cholestyramine in addition t
o MMI (week 0, 14.2 +/- 1.5 ng/ml; week 2, 10.8 +/- 1.2 ng/ml; week 4,
8.9 +/- 1.5 ng/ml). In eight patients who received MMI alone, sIL-2R
decreased less rapidly (week 0, 12.3 +/- 1.4 ng/ml; week 2, 12.3 +/- 1
.3 ng/ml; week 4, 10.9 +/- 1.3 ng/ml), sICAM-1 and sELAM-1 were elevat
ed at baseline but did not decrease during therapy, In the former grou
p, free thyroxine and free triiodothyronine decreased faster, These da
ta show that levels of sIL-2R in serum, but not those of sICAM-1 and s
ELAM-1, mag be of clinical use in the early follow-up evaluation of me
dically treated patients.