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Address correspondence to Professor Paolo Boscolo, Occupational Medicine, G. DAnnunzio University, Via dei Vestini, 66013 Chieti Scalo, Italy; tel 39 0871 355 6704; fax 39 0871 355 6747; e-mail boscolo{at}unich.it.
Zinc (Zn) and selenium (Se) exert regulatory activities on immune functions, while cadmium (Cd) is an immunotoxic agent. The object of this study was to detect effects of 104, 105, and 106 M Cd sulphate, Zn sulphate, and sodium selenite, and their combinations on human peripheral blood mononuclear cell (PBMC) proliferation and IFN-
and TNF-
production. Only 105 M Zn sulphate significantly enhanced spontaneous PBMC proliferation, which was unaffected by the other salts. At 104 and 105 M, Cd sulphate exerted a dose-response inhibitory action on phytohemagglutinin- (PHA-) stimulated PBMC proliferation and cytokine release, while 104 M and 105 M Zn sulphate and 105 M sodium selenite induced a stimulatory effect on both proliferation and cytokine release; 104 M sodium selenite enhanced only the PBMC proliferation; at 106 M, none of the salts changed the PHA-stimulated immune activity. Moreover, 104 and 105 M Zn and 105 M Se strongly upregulated IFN-
(a Th1 cytokine) release, even in presence of 105 M Cd, and reduced the inhibitory effects of Cd on PBMC proliferation and TNF-
release. This study confirms that Zn and Se both strongly enhance cytokine release induced by mitogenic stimulation, showing also that Zn acts with a broader range of concentrations than Se. This suggests that dietary excess of Se may not have beneficial effects.
Keywords: zinc, selenium, cadmium, lymphocyte proliferation, cytokine, immunotoxicity
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