The immune response is regulated by locally released factors, collecti
vely referred to as cytokines. Data on the human immune system have co
nvincingly demonstrated that the hormone prolactin (PRL), in addition
to exerting its endocrine control on the immune system, acts as a cyto
kine in that it is released within the immune system and regulates the
lymphocyte response by paracrine and autocrine mechanisms. Both lymph
ocyte and pituitary PRLs are under the control of immune factors. Synt
hesis of human PRL by lymphocytes is induced by T-cell stimuli, while
increased release of PRL by the pituitary, observed in vivo after immu
ne challenge, may be mediated by cytokines produced by monocyte-macrop
hages. Since hyperprolactinemia and hypoprolactinemia are both immunos
uppressive, physiological levels of circulating PRL must be necessary
to maintain basal immunocompetence. The effects of Cyclosporin (CsA) o
n IL-2 and PRL gene activation and the analysis of the intracellular s
ignaling events downstream IL-2 and PRL receptors suggest coordinate a
ctions of these two cytokines during T cell activation.