Complement system Dr.T.Arivazhagan Department of pathology
Introduction The term complement refers to a system of factors that occurs in normal serum and is activated characteristically by Ag-Ab interaction The system consists of more than 20 proteins Numbered C1 through C9 Functions in both innate & adaptive immunity Defense against microbial pathogens
Definition It is a collection of soluble proteins & membrane receptors that function mainly in host defense against microbes and in pathologic inflammatory reactions
During the process many intermediate products are elaborated Increased vascular permeability Chemotaxis Opsonaisation
Complement system works as a cascade system One reaction triggers the other reaction which triggers others and so on
Complement proteins present as inactive forms Once activated its became a proteolytic enzymes that will degrade the other complement proteins
Most important step in complement activation is Cleavage of C3
Pathway Alternative pathway Classical pathway Lectin pathway
Classical pathway
Alternate pathway Triggered by microbial surface molecules Endotoxin LPS Cobra venom No need of presence of antibodies
Lectin pathway Lectin present in the plasma membrane binds to the carbohydrate on microbes Directly activates the C1
All 3 pathways leads to formation of an active enzyme called C3 convertase Split the C3 into C3a,C3b
C3b Activate C5 convertase Cleave C5 into C5a,C5b
C3a,C5a – Inflammation C3b – Phagocytosis C5b bind with late components C6-C9 Membrane attack complex
Complement will kill the microbes by 3 ways Opsonaisation Inflammation Cytolysis
Opsonaisation C3b and its cleavage products Attach to the microbial cell wall Acts as a Opsonins and promote the phagocytosis by neutrophils and macrophages
Inflammation C3a,C5a products stimulate the histamine release from mast cells Anaphylatoxins Increased vascular permeability and vasodilatation
Cytolysis Deposition of MAC on cells makes them More permeable to water and ions Cell death Important mechanism in killing of microbes with thin cell walls like Neisseria Deficiency of terminal complement predispose to Neisseria infections
Complement activation tightly regulated by cell associated and circulating regulatory proteins C1 inhibitors Blocks the activation of C1 Deficiency – hereditary angioedema DAF & CD 59 DAF inhibit the formation of C3 convertase CD59 inhibit the formation of MAC Deficiency - PNH