-4). In these blocking experiments using the mAbs, the main differences in the results between PBMCs and U937 cells were that the mAbs against TLR-2 and TLR-4 did not block the Sophy -glucan-induced production of IL-8 in the U937 cells. Furthermore, a mAb to the -glucan receptor, Dectin-1, significantly (P<0.05) blocked the Sophy -glucaninduced DNA synthesis in the PBMCs, and Sophy -glucan-induced production of IL-8 in the U937 cells. The Sophy -glucan-induced production of IL-8 in the U937 cells was significantly (P<0.01) blocked by the conventional protein kinase C (PKC) inhibitor Go6976, the novel PKC inhibitor Rottlerin, the protein kinase A (PKA) inhibitor H-89, and the protein tyrosine kinase (PTK) inhibitor herbimycin A. Among these, the blocking effect of the novel PKC (PKC delta isoenzyme) inhibitor Rottlerin was the most pronounced. Studies employing reverse transcriptase-polymerase chain reaction (RT-PCR) showed that Sophy -glucan stimulated the expression of IL-8 mRNA in the U937 cells, and that this induction was inhibited by Rottlerin. Sophy -glucan also blocked the stimulator cell induction of DNA synthesis and IFN-␥ production in the responder cells in a one-way mixed lymphocyte reaction (MLR) using allogenic PBMCs. Interestingly, immunoglobulin G (IgG), but not IgM to Sophy -glucan was detected in the sera derived from normal adult donors and from the umbilical cord blood of neonates. Taken together, these findings strongly suggest that the Sophy -glucan may have unique immune regulatory or enhancing properties that could be exploited by the health food, medical and pharmaceutical industries.