Complement system

3,465 views 22 slides Aug 20, 2019
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About This Presentation

complement system


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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
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