ROLE OF PERIPHERAL CD8 LYMPHOCYTES AND SOLUBLE IL-2 RECEPTOR IN PREDICTING THE DURATION OF CORTICOSTEROID TREATMENT IN POLYMYALGIA-RHEUMATICA AND GIANT-CELL ARTERITIS
C. Salvarani et al., ROLE OF PERIPHERAL CD8 LYMPHOCYTES AND SOLUBLE IL-2 RECEPTOR IN PREDICTING THE DURATION OF CORTICOSTEROID TREATMENT IN POLYMYALGIA-RHEUMATICA AND GIANT-CELL ARTERITIS, Annals of the Rheumatic Diseases, 54(8), 1995, pp. 640-644
Objectives-To determine if the presence of low percentages of CD8 posi
tive cells of high levels of soluble interleukin-2 receptors (sIL-2R)
define a subgroup of patients with more severe polymyalgia rheumatica
and giant cell arteritis (PMR/GCA). Methods-38 PMR/GCA patients were f
ollowed up prospectively. Serum levels of sIL-2R and peripheral blood
CD8 lymphocytes were measured before the start of corticosteroid treat
ment, after six months of treatment and at the last visit. Phenotypica
l analysis of lymphocyte subpopulations was performed with a two colou
r technique, and assay of sIL-2R was performed using an enzyme-linked
immunosorbent kit. Forty four healthy people matched for age and gende
r comprised a healthy control group. Results-The median duration of fo
llow up was 28 months (range 7-65). Corticosteroid treatment lasted a
median of 23.5 months (7-65). Eleven patients (29%) were in remission
at the end of follow up; 45% of the patients had at least one relapse
or recurrence. Compared with controls, patients with active disease ha
d a significantly lower percentage of CD8 cells and significantly incr
eased sIL-2R levels. Erythrocyte sedimentation rate, C reactive protei
n, and sIL-2R values were significantly less after six months of stero
id treatment compared with before treatment. The percentage of CD8 cel
ls remained significantly lower at six months and the end of follow up
compared with controls, while sIL-2R levels remained significantly gr
eater. Patients in whom the percentage of CD8 cells at six months was
lower than one SD of the mean of normal controls (26%) had a significa
ntly longer duration of corticosteroid treatment, a greater cumulative
dose of prednisone and more relapses or recurrences compared with pat
ients in whom the percentage was in the normal range. The duration of
treatment and the cumulative dose of prednisone were not influenced by
the percentage of CD8 cells before treatment therapy or by the levels
of sIL-2R after six months of treatment. Conclusions-A reduced percen
tage of CD8 cells after six months of treatment may be a useful outcom
e parameter which would identify a group of PMR/GCA patients likely to
experience more severe disease, defined as longer duration of cortico
steroid treatment, higher cumulative dose of prednisone, and relapse o
r recurrence of disease.