We tested risperidone and ritanserin, serotonin-S2 receptor antagonist
s, for their effects an in vitro polyclonal IgG and IgM synthesis by h
uman peripheral blood mononuclear cells (PBMC) stimulated with pokewee
d mitogen (PWM). On the basis of the previously reported effect an imm
une function in vivo risperidone in this study was tested in three dif
ferent groups of PBMC: healthy donors as well as schizophrenic patient
s before risperidone treatment and schizophrenic patients after the tr
eatment with risperidone. IgG and IgM production after 7 days of cultu
re was measured by ELISA. Risperidone decreased IgG synthesis (p<0.05)
in PBMC of healthy subjects only at the highest concentration (10(-6)
M) and IgG synthesis enhanced by 5-HT was antagonized by risperidone.
This effect, however, was not statistically significant. Neither risp
eridone nor ritanserin, in the concentration range 10(-8)-10(-6) M, af
fected IgM synthesis in this group. Risperidone did not affect the pro
duction of IgG and IgM by PBMC of schizophrenic subjects in PWM-stimul
ated cultures both before and after risperidone therapy. The spontaneo
us production of IgG in PBMC of schizophrenic subjects before therapy
was decreased (p<0.05) at concentrations 10(-6)-10(-7) M of risperidon
e, We conclude that risperidone and ritanserin did not increase polycl
onal IgG and IgM synthesis in vitro in contrast to neuroleptics curren
tly used in clinical practice.