Staphylococcal Enterotoxin-A(SEA), a 27 kDa monomeric protein, produced by
some strains of Staphylococcus aureus, is a prototype T-cell superantigen w
hich causes proliferation or cytotoxic T-lymphocytes and produces cytokines
like TNF-alpha and IFN-gamma. Recently Protein A (PA), a 42 kDa membrane p
rotein of the Staphylococcus aureus Cowan-I strain, has been termed a B-cel
l super antigen. It has been shown to cause multiple immunological response
s. In the present study we examined the effect of these two superantigens u
sed separately as well as combination in a normal mouse system. It has been
shown that combination treatment of PA and SEA is more effective than that
of each individual one. FACS analyses of cell cycles showed that a finely
turned cellular collaboration occurred in various phases of cell growth and
proliferative response compared with controls (P<0.01). It has also been s
hown that the percentage of various cell types bearing different clusters o
f differentiation markers, e.g., CD8(+), CD34(+) increases considerably due
to the combined effect of PA and SEA. We also observed that co-administrat
ion of both the elicits different soluble mediators like cytokines (TNF-<al
pha>, INF-gamma, IL-1 beta). No apoptotic phenomenon was observed (from the
cell cycle analysis) for the dose of PA and SEA. used for the experiments,
suggesting that these doses of PA and SEA should be non-toxic.