Rd. Huhn et al., PHARMACODYNAMICS OF SUBCUTANEOUS RECOMBINANT HUMAN INTERLEUKIN-10 IN HEALTHY-VOLUNTEERS, Clinical pharmacology and therapeutics, 62(2), 1997, pp. 171-180
Interleukin-10 inhibits T-lymphocyte activation and proliferation and
lipopolysaccharide-induced monocyte production of proinflammatory cyto
kines, Fifty-four healthy volunteers received single doses of recombin
ant human interleukin-10 (1.0, 2.5, 5.0, 10, 25, or 50 mu g/kg) or pla
cebo by subcutaneous injection (randomized double-blind assignment), C
linical adverse events were infrequent at doses below 50 mu g/kg (five
of six subjects had mild flu-like syndrome), Mean serum interleukin-1
0 concentrations were dose related, The mean terminal-phase half-life
ranged from 2.7 to 4.5 hours, and the apparent volume of distribution
ranged from 0.70 to 1.35 L/kg, Hematologic changes included transient
mild to moderate increases of neutrophil counts, decreases of lymphocy
te counts, and a delayed decrease of platelet counts, Recombinant huma
n interleukin-10 significantly suppressed production of the proinflamm
atory cytokines interleukin-1 beta and tumor necrosis factor-alpha by
whole blood stimulated ex vivo with Escherichia coli lipopolysaccharid
e.