Objective. Fibromyalgia(FM) is a clinical entity of unknown etiology f
requently diagnosed in rheumatology. The potential involvement of the
immune system in its pathogenesis has been suggested. Studies of abnor
mal T cell subpopulations often have been inconclusive. We attempted t
o clear this point by comparing lymphocyte subpopulations, including s
ome of the newer activation markers, in patients with FM and healthy c
ontrols. Methods. Sixty-five patients with FM and 56 healthy controls
were studied. Flow cytometry was used as a quantification technique to
measure lymphocyte subpopulations, CD3 (T cells), CD19 (B cells), CD1
6 (natural killer cells), CD4 (T helper/inducer cells), CD8 (T cytotox
ic/suppressor cell), CD25 (interleukin 2 receptor), CD69 (activation i
nducer molecule marker), CD71 (transferrin receptor) and CD54 (ICAM-1)
; CD4/CD8 ratios were also estimated. Results. The number of T cells e
xpressing activation markers CD69 and CD25 was decreased in patients w
ith FM; the other subpopulations were similar in patients and controls
. Conclusion. Our results suggest a defect in T cell activation in pat
ients with FM.