Background: Neuroendocrine factors play an important role in the expre
ssion of autoimmune diseases. Prolactin (PRL) can induce T-cell prolif
eration and macrophage activation. Elevated PRL levels have been descr
ibed in patients with rheumatoid arthritis (RA). Aim and Methods: We s
tudied immunological and clinical effects of PRL suppression in 9 RA p
atients with active disease, treated for 3 months with bromocriptine (
BRC), an inhibitor of PRL secretion. Results: BRC induced a significan
t depression of the peripheral blood mononuclear cells response to ant
igen (p=0.008) and mitogen (p=0.008) which was significantly correlate
d with improvement in the HAQ disability index (r=0.68; p=0.04) and gr
ip strength (r=0.7; p=0.02). Also, the in-vitro production of IL-2, ni
tric oxide and poliamines-that are critical for the proliferative resp
onse of lymphoid cells- decreased significantly. The group experienced
significant improvement of grip strength (p=0.028) and the HAQ disabi
lity index (p=0.025), whereas 4 individuals achieved clinical improvem
ent according to the American College of Rheumatology preliminary defi
nition. We conclude that BRC treatment induces a significant depressio
n of in-vitro immune function in RA patients and that these changes ar
e related to parameters of disease activity. The effects of BRC on imm
une function and disease activity in RA patients warrant further inves
tigation.