Be. Barton et al., INTERLEUKIN-6 AND INTERLEUKIN-11 PROTECT MICE FROM MORTALITY IN A STAPHYLOCOCCAL ENTEROTOXIN-INDUCED TOXIC SHOCK MODEL, Infection and immunity, 64(3), 1996, pp. 714-718
BALB/By mice given doses of D-galactosamine plus Staphylococcus aureus
enterotoxin B die within 48 h of administration. The cause of death i
s a syndrome much like toxic shock syndrome in humans. We used this mo
del to investigate the role of two cytokines, interleukin 6 and interl
eukin 11, which share the signal transducing subunit, gp130, of their
respective receptors. We observed that pretreatment of mice with antib
ody to interleukin 6 increased mortality from 55% to nearly 90% (P < 0
.001), while pretreatment with either cytokine reduced death. The prot
ection was dose dependent; however, interleukin 6 was about 10-fold mo
re potent than interleukin 11. These data indicate that endogenous int
erleukin 6 plays a protective role in attenuating acute inflammatory r
esponses; furthermore, interleukin 6 and interleukin 11 can abrogate T
-cell activation due to triggering by superantigen. A possible clinica
l role for these cytokines in the treatment of toxic shock merits furt
her investigation.