H. Bessler et al., SIGNIFICANT INHIBITION OF SPONTANEOUS IGA SECRETION BY SELECTIVE PERIPHERAL-TYPE BENZODIAZEPINE RECEPTOR LIGANDS, Clinical neuropharmacology, 20(3), 1997, pp. 215-223
The in vitro effect of benzodiazepine (BZ) receptor ligands on the sec
retion of immunoglobulin isotypes IgM, IgG, and IgA by human periphera
l blood mononuclear cells (PBMCs) was examined. It was found that the
specific peripheral-type BZ receptor (PER) ligands (Ro5-4864 and PK 11
195) inhibit the spontaneous secretion of IgA by human PBMCs in a dose
-dependent manner, in the micromolar range. The decreased secretion of
IgG and IgM induced by these ligands did not reach significant levels
. The mixed BZ ligands (diazepam and flunitrazepam) had no consistent
or significant effect on the production of the three immunoglobulin is
otypes tested in the current study. The central-type ligand (clonazepa
m) did not affect IgM, Igc, or IgA secretion. The significant inhibito
ry effect of PER ligands was confined to the spontaneous secretion of
IgA by human PBMCs, and no such effect was detected in cells stimulate
d by pokeweed mitogen to produce immunoglobulins. It seems that PER li
gands are capable of suppressing spontaneous IgA secretion, but fail t
o affect the augmented production induced by mitogen.