A number of studies documented that the heavy metals are not only toxic for
the organisms but they may modulate immune responses. The immunomodulatory
activity was proved in several irt vivo and bl vivo model systems. In the
current study, immunomodulatory activities of lead and cadmium are presente
d. The viability of both lymphocytes and macrophages was affected by heavy
metals in a dose- and time-dependent manner. Tn the case of lead, the depre
ssion of N-oxide production closely correlated with increased blast transfo
rmation of spleen cells induced by concanavalin A (ConA), On the contrary,
cadmium suppressed the production of N-oxides but stimulated significantly
the proliferation of spleen cells. The production of cytokines by lymphocyt
es and macrophages was dependent on the in vitro model used. Generally, the
treatment of macrophages with lead results in disregulation of the product
ion of proinflammatory cytokines \tumour necrosis factor alpha (TNF-alpha),
interleukin \alpha (IL-1 alpha) and interleukin 6 (IL-6)\ and preferential
production of Th1 type of cytokines (IFN-gamma and IL-2), Cadmium seemed t
o trigger the Th2 cytokine regulatory pathway \interleukin 4 (IL-4), interl
eukin 10 (IL-IO)\. The results suggest the metal-induced changes in immunor
egulatory mechanism of host with potentially severe clinical consequences.
(C) 2000 Elsevier Science Ltd. AII rights reserved.