Sepsis, complement and the dysregulated inflammatory response

• Introduction - Models of sepsis - Evidence for complement activation in sepsis - Protective effects of C5a generated in limited amounts - Sepsis-induced changes in signalling cascades - Divergent effects on phagocytic cells during sepsis - Harmful effects of C5a and C5a receptors in experimental sepsis • Future directions Sepsis in human beings is a major problem involving many individuals and with a high death rate. Except for a single drug (recombinant activated protein C) that has been approved for treatment of septic patients, supportive measures represent the main clinical approach. There are many models of experimental sepsis, mostly in rodents. A commonly used model is cecal ligation and puncture (CLP). In this model, robust activation of complement occurs together with up-regulation of C5a receptors (C5aR, C5L2) in a variety of different organs (lungs, kidneys, liver, heart). In septic human beings there is abundant evidence for complement activation. Interception of C5a or its receptors in the CLP model greatly improves survival in septic rodents. There is compelling evidence that CLP causes an intense pro-inflammatory state and that C5a interaction with its receptors can be linked to apoptosis of the lymphoid system and cells of the adrenal medulla, loss of innate immune functions of blood neutrophils, consumptive coagulopathy and cardiac dysfunction. These findings may have implications for therapeutic interventions in human beings with sepsis.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/74963/1/j.1582-4934.2009.00893.x.pd