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Address correspondence to Professor Mario Di Gioacchino, Section of Occupational Medicine, Allergy and Clinical Immunology, G. DAnnunzio University, Via dei Vestini, 66013 Chieti Scalo, Italy; tel 39 087 135 8578; fax 39 087 155 1615; e-mail m.digioacchino{at}unich.it.
In vitro immune effects of Pt compounds of occupational and/or environmental importance, or those used in cancer treatment were studied. Spontaneous and PHA-stimulated proliferation of peripheral blood mononuclear cells (PBMC) and in vitro release of TNF-
, IFN-
, and IL-5 were assessed in presence of high and very low concentrations of Pt salts: 104 and 107 M (NH4)2[PtCl6], (NH4)2[PtCl4], PtCl4, PtCl2, Na2PtI6, and cis-diaminedichloroPt (CisPt). Spontaneous and PHA-stimulated PBMC proliferation were both inhibited by 104 M (NH4)2[PtCl6] and (NH4)2[PtCl4], while only PHA-stimulated proliferation was inhibited by 104 M CisPt, without significant effects of the other Pt salts. TNF-
release from PBMC was reduced by 104 M (NH4)2[PtCl6] and INF-
release was reduced by 104 and 107 M hexa- and tetrachloroplatinate and 104 M Na2PtI6, but not by other Pt salts. IL-5 release (related to the Th2 immune response) was inhibited by 104 M (NH4)2[PtCl6], (NH4)2[PtCl4] and Na2PtI6, but it was enhanced by both 104 and 107 M PtCl4. PtCl2 did not influence the immune effects. The study shows Pt salts have immune effects and their potency is ranked in the following order: (NH4)2[PtCl6] > (NH4)2[PtCl4] > Na2PtI6 and CisPt > PtCl4 > PtCl2. These results indicate that certain Pt salts affect lymphocyte proliferation and cytokine release. The intracellular mechanisms responsible for such effects have not been identified.
Keywords: platinum, lymphocyte proliferation, cytokines, immunotoxicity, allergy
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