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what is the complement system
major effector system of the humoral branch of the innate and adaptive immune response
inflammation, phagocytosis and membrane attack
how do some activated proteins bind covalently to bacteria opsonising them
phagocytosed by cell with complement receptors
what do terminal components of the complement system generate
the membrane attack complex (MAC) → lysis of the pathogen
what is the classical pathway of activation
initiated by antigen: antibody complexes
what is the alternative pathway of activation
triggered by some pathogen surfaces
what is the lectin pathway of activation
initiated by acute phase proteins that bind glycoproteins or carbohydrates on micro-organisms
what do routes for the pathways all generate
C3 convertase
leads to opsonisation of antigen, inflammatory response and production of the membrane attack complex
what is the first component of the classical pathway activation
C1
C1q, C1r, C1s
2 molecules of C1r and C1s bind to each C1q
when is activation of the classical pathway initiated
when antibodies bind to the surface of an antigen or pathogen bound C1q
what is C3 convertase
C4b2a
what forms C3
C3a and C3b
what is C3b
opsonin
also involved with C5 convertase
what is C5 convertase
C4b2a3b
what is C5 made of
C5a and C5b
how is the alternative pathway activated
by action of the classical or lectin pathway
spontaneous hydrolysis of C3
what does C3b bind to
factor B
what does factor D cleave into
Ba and Bb
what does factor P do
properdin
stabilises
what receptors does the lectin pathway use
soluble (acute phase proteins)
what does MASP-2 cleave
C4 and C2
what complexes does the lectin pathway get
mannose binding lectin and MBL-associated serine proteases
MASP-1 and MASP-2
what does C3 do
opsonisation, inflammation and cytolysis
what is the clinical consequence of C3
life-threatening infections with a range of bacteria
what is the function of C6, C7, C8 and C9
cytolysis
what is the clinical consequence of C6, C7, C8, and C9
problems with infection with Neisseria