Abstract:
Objective:To investigate the effects of low dose of dexamethasone on CD11b
+ Gr-1
+ myeloid-derived suppressor cells(MDSCs) in septic mice induced by lipopolysaccharide(LPS).
Methods:The septic mice model was established by the intraperitoneal injection of LPS in BALB/c mice.The mice were randomly divided into the normal control group(NC group), sepsis group(SE group) and sepsis combined with dexamethasone group(SD group).The levels of serum interferon-γ and interleukin-10 were detected at 6, 12 and 24 hours.The percentage of CD11b
+ Gr-1
+ MDSCs in spleen and bone marrow of mice were detected at 12, 24, 48 and 72 hours.
Results:Compared with the NC group, the levels of interferon-γ at 6 hours and interleukin-10 at 12 hours in SE group and SD group increased significantly(
P<0.05 to
P<0.01), and the difference of which between SE group and SD group was not statistically different (
P<0.05).Compared with the NC group, the percentages of MDSCs in spleen at 12 to 72 hours in SE group and at 12 to 48 hours in SD group increased significantly (
P<0.01), and the differences of the percentage of MDSCs at 24 to 72 hours between SE group and SD group were statistically different (
P<0.05).Compared with the NC group, the percentages of MDSCs in bone marrow of SE and SD group increased significantly at 48 hours and 72 hours (
P<0.05 to
P<0.01).the differences of which at 48 and 72 hours between SE and SD groups were statistically significant(
P<0.05 and
P<0.01).
Conclusions:Low dose of dexamethasone can inhibit the production and accumulation of MDSCs in septic mice induced by LPS.