Ma. Gutierez et al., PROLACTIN, A LINK BETWEEN NEUROENDOCRINE AND IMMUNE-SYSTEM - ITS ROLEIN THE PATHOGENESIS OF RHEUMATIC DISEASES, Revue du rhumatisme, 61(4), 1994, pp. 278-285
Increasing evidence suggest that prolactin (PRL) has important immunor
egulatory properties and may play a role in the pathogenesis and disea
se expression of certain autoimmune diseases. Prolactin is co-mitogeni
c on murine and human lymphocytes, induces the formation of IL-2 cell
surface receptor and modulates the expression of various growth factor
related genes. Prolactin also stimulates antibody production both in
vivo and in vitro. Specific high affinity prolactin-receptors have bee
n described on T and B lymphocytes as well as on monocytes. They are d
istributed on heterogeneous lymphocyte subsets and they showed imbalan
ce in autoimmune situations. Lymphocytes may produce PRL-like proteins
biologically active that function as autocrine growth factors for lym
phoproliferation. Hyperprolactinemia has been found in male patients w
ith systemic lupus erythematosus (SLE) and also during pregnancy in SL
E patients. Hyperprolactinemia is correlated with clinical and serolog
ical activity in a subset of SLE patients. High levels of PRL aggravat
es disease activity and accelerates mortality in the B/W mouse model o
f SLE. In rheumatoid arthritis an excessive and upregulated secretion
of PRL has been shown. Hyperprolactinemia has also been shown in a sub
set of patients with primary Sjogren's syndrome. High PRL levels have
been found in Reiter's syndrome patients and bromocriptine treatment h
as been reported effective in these patients and psoriatic arthritis p
atients. These data support a potential role of this immunoregulatory
hormone in the pathogenesis of some rheumatic diseases.