CI-959 is an orally effective inhibitor of cellular activation in both
in vitro and animal models, To assess the effects of CI-959 on immune
function, male Fischer 344 rats were evaluated for splenic T- and B-l
ymphocyte populations, antibody-forming cell response to sheep red blo
od cells (sRBC), concanavalin A and pokeweed mitogen-induced lymphocyt
e proliferation, Natural Killer cell activity, and reticuloendothelial
system clearance of sRBC. Host resistance was measured in female B6C3
F1 mice using Listeria monocytogenes, Streptococcus pneumonia, and B16
F10 melanoma models, CI-959 was administered to both species of rodent
s at 25, 50, and 75 mg/kg/day for 14 days, A vehicle control and two p
ositive controls (cyclophosphamide and dexamethasone) were run concurr
ently, CI-959 generally did not suppress immunological responses in ra
ts at doses lower than those which also altered body weight gain and r
educed spleen and thymus weights, Natural Killer cell activity was sig
nificantly reduced at 50 and 75 mg/kg CI-959. At 75 mg/kg rats also ex
hibited a reduction in ability to make anti-sRBC antibody. The number
of T- and B-lymphocytes, proliferative response to mitogens, and macro
phage activity of the reticuloendothelial system were not affected by
CI-959, CI-959 also did not alter resistance of mice to Listeria monoc
ytogenes, Streptococcus pneumoniae, or B16F10 melanoma cells, Based on
these ex vivo and in vivo assays, the rodent immune system does not a
ppear to be a sensitive or toxicologically important target for CI-959
.