Fig. 1From: IL-33 receptor (ST2) deficiency downregulates myeloid precursors, inflammatory NK and dendritic cells in early phase of sepsisDeletion of ST2 accelerates CLP induced polymicrobial sepsis and affects granulocytes influx into peritoneal cavity. Clinical score and survival rate of septic ST2−/− and WT mice was monitored every 6 h. a ST2−/− mice exhibit significantly increased clinical score during first 18 h following CLP. b Survival rate of septic ST2−/− and WT mice was analyzed by Fisher’s exact test for each time point. ST2−/− mice had significantly decreased survival rate at 36, 42 and 48 h following CLP (n = 22 mice per group). c Significantly decreased number of peritoneal cells in septic ST2−/− in comparison with WT mice 12 h following CLP. The number of peritoneal neutrophils (CD11b+Ly6G+) (d), eosinophils (CD11b+Siglec-F+) (e), mast cells (CD117+FcεRI+) (f) and macrophages (g) 12 h following CLP. Data are presented as mean ± SE, n = 4–7 mice per group. *p < 0.05, **p < 0.01Back to article page