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Complement pathways: Classical pathway Alternative pathway Lectin pathway. Complement proteins. Classical pathway C1q C1r C1s C4 C2Alternative pathway D C3 BLectin pathway MBL MASP-1 MASP-2Membrane attack complex(MA
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3. Complement proteins Classical pathway
C1q C1r C1s C4 C2
Alternative pathway
D C3 B
Lectin pathway
MBL MASP-1 MASP-2
Membrane attack complex(MAC)
C5 C6 C7 C8 C9
Membrane regulatory proteins
CD55 CD46 CD59
4. Soluble regulatory proteins Positive regulation Properdin Negative regulation C1-INH C4-bp Factor H Factor I Carboxypeptidase S protein Clusterin
5. Comparison of the classical and alternative complement pathways
8. Complement pathway activators Classical pathway
IgM-containing immune complexes
IgG-containing immune complexes
Mannose-binding lectin(MBL)
C-reactive protein(CRP)
Serum amyloid P(SAP)
Myocardial damage products
Membranes of apoptotic cells
C4 nephritic factor (C4Nef)
Myelin
9. Alternative pathway
Tickover
Amplification from classical pathway C3b fixation
Repeating polysaccharides
Endotoxin
Virally infected cells(measles,influenza,Epstein-Barr virus)
IgA-containing immune complexes
Some Ig light Chains
C3 nephritic factor(C3Nef)
Cobra venom factor(CVF)
Zymosan(yeast cell wall)
Lectin pathway
Repeating simple sugars
10. Complement-fixing potential of antibodies Classical pathway:
IgM>IgG3>IgG1>IgG2>>IgG4
IgA can activate the alternative pathway
IgE will activate complement only in unusual circumstances
11. Structural and functional homologs in activation pathways
C2 and factor B
C1q and mannose-binding lectin(MBL)
C1r/C1s and MASP-1/MASP-2
C3/C4/C5
C6/C7/C8/C9
12. Complement regulatory proteins and primary locations Fluid phase
C1-INH
Factor I
Factor H
C4b-binding protein (C4-bp)
S protein(vitronectin)
SP-40,40(clusterin)
Carboxypeptidase
13. Cell membrane
Decay-accelerating factor(DAF,CD55)
Membrane cofactor protein(MCP,CD46)
CD59
Membrane C3-proteinases
Matrix
Decorin
14. Complement pathway regulatory mechanisms and examples of each
Protease inhibitors
C1r:C1-INH
C1s:C1INH
15. Complement pathway regulatory mechanisms and examples of each Proteases
C4a
C3a Carboxypeptidase Inactivated
C5a
16. Complement pathway regulatory mechanisms and examples of each Decay-acceleration
DAF,C4-bp,CR1 C2a
C4b2a C4b
DAF,H,CR1 Bb
C3bBb C3b
17. Complement pathway regulatory mechanisms and examples of each Cofactor activity
Factor I
C3b C3bi
MCP,H,CR1
FactorI
C4b C4bi
MCP,C4-bp,CR1
18. Complement pathway regulatory mechanisms and examples of each Inhibition of assembly
C1:Decorin
C5b-C7:S protein
C5b-C7:SP-40,40
C5b-C9:CD59
C9polymerization:CD59
19. Complement receptors
C1q receptor
Complement receptor 1(CR1)
Complement receptor 2(CR2)
Complement receptor 3(CR3)
Complement receptor 4(CR4)
C5a,C3a and C4a receptors
20. Anaphylatoxins and disease Target
Smooth muscle
Mast cells
Blood capillary wall
Vascular endothelium
Leukocytes
Platelets
Immune response Effect
Contraction
Histamine release
Increase in vascular permeability
Increased adhesiveness for leukocytes
Adhesion,aggregation,chemotaxis,release of lysosomal enzymes,generation of oxygen radicals
Aggregation,release of serotonin
C3a:suppression
C5a:enhancement
21. Complement as an effector pathway in disease
22. Vasculitis and immune complex diseases
Polyarteritis nodosa(PAN)
Hypersensitivity vasculitis
Henoch-Schonlein purpura(HSP)
Rheumatoid vasculitis
Systemic lupus erythematosus(SLE)
23. Rheumatologic disease
24. Pulmonary disease
Acute respiratory distress syndrome
SLE
25. Platelet diseases
Idiopathic thrombocytopenic purpura
(ITP)
26. Hemolytic disease
Paroxysmal nocturnal hemoglobinuria (PNH)
Hemolytic-uremic syndrome
(HUS)
27. Myocardial disease
Unstable angina
Myocardial infarction
Reperfusion injury
28. Renal disease(Glomerulonephritis)
29. Atherosclerosis
30. Cutaneous disease
SLE
Phototoxic reactions
Autoimmune bullos diseases
Acne
Psoriasis
31. Systemic lupus erythematosus
32. Reproduction and pregnancy
33. Myositis
Dermatomyositis
34. Neurologic disease
Multiple sclerosis
SLE
Guillian-Barre syndrome
Alzheimer’s disease
35. Xenotransplant rejection
36. Diseases in which complement inhibitors will probably be effective Some forms of vasculitis
Rheumatoid arthritis
ARDS
SLE
Many types of renal diseases
ITP
Hemolytic anemia
Myocardial infarction
Neurologic disease
Ischemia-reperfusion injury
Antiphospholipid syndrome
Recurrent immune-mediated fetal loss
Ab-mediated cutaneous disease
Xenotransplant rejection
37. Complement deficiencies
38. Clinical presentation of complement deficiencies
Infection
Autoimmune disease
39. Summary of complement deficiency states
40. Summary of complement deficiency states