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22 Cards in this Set
- Front
- Back
Interaction of antibodies with antigens can result in?
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-removal of toxins
-coating a pathogen to inhibit invasion of host -initiation of an effector mechanism |
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Basic features of the complement system are?
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-about 30 proteins circulating in the blood
-precursors are cleaved by enzyme and then become enzyme (serine proteases) -ever expanding cascade of actions |
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The complement system consists of three major pathways?
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Classic
Alternate Membrane Attack |
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The Classic Complement pathway is stimulated by what and where?
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-C1q binding to one IgM or many IgG
-on a cell surface *or* in the plasma |
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C1 exists where and consists of what?
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in plasma as free floating
2C1r, 2C1s, 6C1q |
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C1r does what?
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Cleaves C4 into C4a and C4b,
Cleaves C2 into C2a and C2b |
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C3 convertase complex can be formed by?
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C3b*Factor B (C3b*Bb), or
C4b*2b |
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C4b binds where and what and how to each?
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-covalently to sugar residues on cell-surface glycoproteins
-non-convalently to C2b |
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C4b2b is known as
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-C3 convertase, and
-C3/C5 convertase |
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C3 is cleaved by whom into what?
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-C3 convertase (C4b2b or C3b*Bb) into C3a and C3b
-can also spontaneously cleave |
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C3a, C4a, and C5a are what?
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anapholotoxins
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C3b binds where to attract what and therefore can be known as?
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Binds covalently to *glycoproteins* scattered across a cell or other surface.
Attracts Macrophages and Neutrophils to the C3b-coated cell or particle preparatory to phagocytosis. This effect qualifies C3b as an opsonin. Also binds to C5 to become a C5 convertase. Also binds to Bb to become a C3 convertase or to C3bBb to become a C5 convertase |
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C5b binds what to form what to allow?
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1 C6, 1 C7, 1 C8 and up to 19 C9 to form the membrane attack complex allowing enterance of ions into cell.
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Factor B can bind to what forming what?
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C3b*Bb - Factor C3 convertase
C3b*Bb*C3b - Factor 5 convertase and thus membrane attack complex |
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Self is protected by C3b by
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sialic acid on outside of cells
downregulation of complement activity |
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Complement activity is downregulated by?
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Factor H binding to Factor B, Breaking feedback loop
Factor I, Inactivating C3b C1INH, inhibiting cleavage of C2 and C4 by C1 |
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Genetic disorders of complement products include?
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C3 or C9 deficiency - prone to bacterial infections
C1,C2,C4 (early products) - autoimmune such as Lupus C1INH - some sort of crazy edema |
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Breakdown of C3b results in production of what that is taken in by?
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C3d is taken in by dendritic cells and B cells.
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C3d antigen complex enters B cells with the same receptor as this pathogen?
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Epstein-Barr Virus
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The EBV can cause what?
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mononucleosis
Burkitt's lymphoma |
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complement-mediated lysis can cause such serious disorders as
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Rh disease
immune hemolytic anemia (SLE) immune thrombocytopenic purpura |
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Complement effector functions include
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solubilizing antibodies - early products
vascular permeability -C3a, C5a attracting phagocytic cells -C5a cell lysis opsonization aiding in phagocytosis -C3b |