Although the experimental administration of IL-1 induces several aspec
ts of the inflammatory response, such as fever, tachycardia, and acute
phase proteinemia, the contribution of IL-1 to the human responses to
injury or infection remains unclear. A specific IL-1R antagonist (IL-
1ra), which effectively blocks the actions of IL-1, was utilized to ev
aluate the influence of endogenous IL-1 during experimental human endo
toxemia. Eighteen healthy volunteers each underwent one control study
day, followed 3 days later by one of three randomly chosen treatments:
a 6-h infusion of IL-1ra alone (133 mg/h), 20 U/kg national reference
endotoxin alone, or both endotoxin and IL-1ra infusion. IL-1ra admini
stration alone was not associated with any observable response. Despit
e achieving high circulating levels of IL-1ra (34 +/- 3 mu g/ml), ther
e were no significant differences in hemodynamic parameters, core temp
erature, or resting energy expenditure in those endotoxemic volunteers
receiving IL-1ra when compared with those who did not. Furthermore, l
eukocyte kinetic and circulating cytokine, acute phase protein, and en
docrine responses were similar in both endotoxemic groups. However, IL
-1 blockade did significantly reduce the subjective severity of sympto
ms experienced by the endotoxemic volunteers (p < 0.05). This study de
monstrates that an endogenous IL-1 response does not play a significan
t role in the hemodynamic, immunologic, and metabolic responses to mil
d endotoxemia in humans.