immune system
• using model of P. acnes infection in vivo, Th1 responses was reduced compared to wild type, similar to that of Cebpb deficient Cebpbtim1Kish homozygous mice
|
• in vitro, LPS-stimulated mutant peritoneal macrophages exhibit impaired production of G-CSF and bioactive IL-12p70, whereas IL-12p40 is overproduced
|
• using model of P. acnes infection in vivo, homozygous mutant mice are strongly resistant to LPS-induced endotoxin shock compared to wild type, similar to that of Cebpb deficient Cebpbtim1Kish homozygous mice
|
• using model of P. acnes infection in vivo, granuloma formation was reduced compared to wild type, similar to that of Cebpb deficient Cebpbtim1Kish homozygous mice
|
• homozygous mice are susceptible to infection by Listeria monocytogenes in vivo compared to wild type, but milder than that of Cebpb deficient Cebpbtim1Kish homozygous mice
• in vitro, LPS-stimulated mutant peritoneal macrophages exhibit no increased susceptibility to Listeria monocytogenes infection
|
hematopoietic system
• using model of P. acnes infection in vivo, Th1 responses was reduced compared to wild type, similar to that of Cebpb deficient Cebpbtim1Kish homozygous mice
|
• in vitro, LPS-stimulated mutant peritoneal macrophages exhibit impaired production of G-CSF and bioactive IL-12p70, whereas IL-12p40 is overproduced
|