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39 Cards in this Set

  • Front
  • Back
alternative pathway of complement
pathway initiated by C3b, associated with innate immunity
anaphylatoxin
C3a, C4a, C5a; binding to their receptors on mast cells and basophils induces cell degranulation
anaphylatoxin inhibitor
protein that inactivates the anaphylatoxins
Ba and Bb
proteolytic fragments of Factor B following cleavage by Factor D; Bb forms part of the AP C3 convertase
C1 INH
C1 inhibitor protein
protein that binds to C1 preventing its activation (C1 cleaves C4 and C2)
C1 through C9
proteins of the classical pathway
C2b
proteolytic fragment of C2 that is also a weak kinin (increases vascular permeability)
alternative pathway C3 convertase
C3bBb
classical pathway C3 convertase
C4b2a
C3 tickover
refers to the spontaneous production of C3b which activates complement AP
C3a, C4a, C5a
proteolytic fragments of C3, C4, C5, respectively that are also anaphylatoxins
C3b
an opsonin that activates AP; a component of both AP and CP
C4bp
a regulatory protein that binds C4b, preventing its attachment to cells and also promotes the dissociation of AP C3 convertase
AP C5 convertase
C3bBbC3b
CP C5 convertase
C4b2a3b
CD59
MAC inhibitor
classical pathway of complement
pathway initiated by IgM or IgG immune complexes
CR1
complement receptor 1 for C3b
CR2
complement receptor 2 for C3bi
CR3a/4a
complement receptor for anaphylatoxins C3a and C4a
DAF
decay accelerating factor
prevents formation of, or causes dissociation of C3 convertases by binding to C4b and C3b
CR5a
complement receptor of the anaphylatoxin C5a
Factor B
binds to deposited C3b
Factor D
enzyme that cleave bound Factor B
Factor H
binds C3b which prevents binding of Factor B to C3b and causes dissociation of C3bBb
Factor I
regulatory protein that cleaves soluble forms of C3b and C4b in the presence of one of several cofactors
GPI
glycosyl-phosphatidyl-inositol
molecule that serves to attach some proteins to the cell in lieu of a transmembrane domain
HAE
hereditary angioedema
complement disorder caused by genetic deficiency of C1 INH
HRF
homologous restriction factor
MAC inhibitor
kallikrein
formed during intrinsic coagulation pathway activation
kininogen
cleaved by kallikrein to create bradykinin
MAC
membrane attack complex
complex made up of C5b, C6, C7, C8, and C9; inserts into membranes to induce cell lysis
Neisseria species
MAC protein deficiencies (esp. C8) results in recurrent infections with these particular bacterial species
paroxysmal nocturnal haemoglobulinuria
genetic disorder that manifests as hemolytic anemia due to defect in GPI linkages
properdin
protein that stabilizes AP C3 convertase
S protein
MAC inhibitor
terminal pathway
convergence of AP and CP leading to MAC formation
vitronectin
MAC inhibitor
xenograft
graft from another species