Certain strains of Staphylococcus aureus express one or both of two related
, but immunologically distinct, exfoliative toxins (ETA and ETB), These tox
ins induce the symptoms associated with staphylococcal scalded skin syndrom
e, Both ETs have been shown to stimulate T cell proliferation. Recently, it
was reported that ETA, is a superantigen that stimulates T cells bearing h
uman V beta 2 or several murine V beta s. However, other investigators have
proposed that the superantigenicity reported for ETA resulted from contami
nants in commercial preparations. This present study addresses those confli
cting reports by assessing the biological and immunologic activities of hig
hly purified rETs, ETA and ETB required APCs to induce selective polyclonal
expansion of several human V beta s (huV beta s), although, neither toxin
expanded huV beta 2. ETB induced expansion of murine T cells bearing V beta
s 7 and 8. those that have the highest homology to the huV beta s expanded
by ETA and ETB. Although how cytometry of ETB-stimulated T cells matched P
CR results, stimulation by ETA reduced percentages of T cells positive for
several huV beta s that had been shown to hare increased levels of mRNA tra
nscripts. Elh and ETB induced contrasting reactions in vivo. In rabbits, ET
B was moderately pyrogenic and enhanced susceptibility to lethal shock, whi
le ETA lacked both activities, Predictions based on comparisons with other
superantigens suggest molecular regions potential?, involved in receptor bi
nding in the ETA crystal structure and a modeled ETB three-dimensional stru
cture. These results show that ETs are superantigens with unique properties
that could account for the discrepancies reported.