M. Jontell et al., EFFECTS OF UNPOLYMERIZED RESIN COMPONENTS ON THE FUNCTION OF ACCESSORY CELLS DERIVED FROM THE RAT INCISOR PULP, Journal of dental research, 74(5), 1995, pp. 1162-1167
Monomeric resin components from dental composites are toxic to fibrobl
asts in culture and thus may interfere with the local immune system of
the pulp, reducing its effective defense potential, either by cytotox
icity or by a more specific immune mechanism. Therefore, the present s
tudy was undertaken to observe the cytotoxic effects elicited by certa
in unpolymerized components of resin composites upon the function of a
ccessory pulp cells in mitogen-induced proliferation of T-lymphocytes.
Accessory cells from the rat incisor pulp were released following enz
ymatic digestion with collagenase. The assay included incubation of th
ese cells with purified T-lymphocytes from cervical lymph nodes for 72
h in the presence of different concentrations of the resin components
. The proliferative T-lymphocyte response was monitored by H-3-thymidi
ne incorporation. Initially, we conducted experiments on spleen cells
to determine the proper concentration intervals for suitable testing o
f the resin components. To assess the individual susceptibility of acc
essory cells and T-lymphocytes, we pre-treated each of these cells wit
h some of the test materials prior to assay. At low concentrations, ur
ethane dimethacrylate (UDMA), bis-glycidyl methacrylate (bis-GMA), tri
ethylene glycol dimethacrylate (TEGDMA), and bis-phenol A (BPA) increa
sed spleen cell proliferation to concanavalin A (con A). Purified T-ly
mphocytes stimulated by pulpal cells did not show enhanced responses t
o UDMA, bis-GMA, glycidyl methacrylate (GMA), or N,N-dihydroxyethyl-p-
toluidine (DHEpT). At higher concentrations, all substances except cam
phoroquinone (CAMP) showed inhibitory effects in both test systems. Th
e in vitro study shows that resin components can evoke either immunosu
ppression or immunostimulation on mitogen-driven proliferation of puri
fied T-lymphocytes and spleen cells.