Objective. Soluble CD4 (sCD4) and sCD8 were measured in the sera of 19
patients with active polymyalgia rheumatica (PMR). Methods. We correl
ated the results obtained with lymphocyte subpopulations, soluble inte
rleukin 2 receptors (sIL-2R), and clinical and laboratory variables at
diagnosis. In addition 15 patients were prospectively studied during
a 6 month period of prednisone therapy. Assays of the sCD4 and sCD8 mo
lecules and of the sIL-2R were performed using an enzyme-linked immuno
sorbent kit. Results. Serum sCD8 and sIL-2R levels were significantly
elevated in patients with active disease compared to normal controls,
while serum sCD4 and the relative percentage of CD8 + T cell levels de
creased. In the 15 patients prospectively studied sCD8 levels fell sig
nificantly after 1 week of therapy along with the remission of clinica
l disease and normalization of erythrocyte sedimentation rate. At the
end of the study period, sCD8 values did not differ from normal contro
ls and they were significantly reduced compared to baseline values. CD
8+ lymphopenia persisted at the end of the study. sCD4 levels remained
significantly lower during the study period. slL-2R levels fell signi
ficantly at the end of the study period. However, the 6-month levels o
f sIL-2R remained significantly higher compared to controls. Conclusio
n. The rise of serum sCD8 levels observed in patients with PMR with ac
tive disease suggests an early activation of CD8 T cells. The therapeu
tic effect of steroid in PMR may be partially mediated by its effect o
n CD8 activated cells.