Complement Flashcards

1
Q

Classical pathway order

A

1r/q/s, 4, 2, 3, 5, 6/7/8/9

  • C6,7,8 and 9 bind to the activated C5, forming the membrane attack complex
  • C 8 is the one that first inserts itself into the membrane
  • C9 polymerizes and forms a pore on the membrane surface
  • creates lesions which kill the cell via a inrush of fluids
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2
Q

opsinization and complement

A

coating of organisms with antibody and C3b so that they are more easily phagocytosed by neutrophils and macrophages (can do it alone but is much slower)

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3
Q

chemotaxis in completment

A
  • C3a and C5a

- phagocytic cels are attracted to the site of the antigen

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4
Q

anaphylatoxin production and complement

A
  • C3a and C5a degranulate mast cells and basophils

- granules contain potent inflammatory chemicals eg histamine

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5
Q

lysis of organsims and complement

A

-coated with specific antibody and recruit C8 and C9

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6
Q

inhibitor of the classical complement pathway

A

-C1-inhibitor

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7
Q

alternative complement pathway

  • how is it activated
  • proteins involved
A
  • by bacterial or viral products (LPS)
  • proteins involved: C3b, factor B and D, properdin
  • together generate C3bBbP which splits c3 into C3 and Cb and continues the the classical cascade
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8
Q

inhibitors of the alternative pathways

A

-Factor H and Factor I are inhiibitors of the alternative pathway and regulate the activation of the system

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9
Q

lectin pathway

A
  • activated by organisms with mannose on their surface
  • proteins involved: MBL (mannose binding lectin), MASP1, MASP2, C4, C2
  • C4b2b cleave C3 and this cascade enters the classical pathway
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10
Q

absence of C1q, C2, or C4

A

-associated with SLE

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11
Q

absence of C3

A

-severe recurrent bacterial infection

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12
Q

absence of C5

A

-bacterial infection

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13
Q

absence of C6,7,8

A

overwhelming neisserial infection

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14
Q

absence of alternative pathway components

A

-recurrent bacterial infections

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15
Q

absence of lectin pathway proteins

A

-infection in childhood

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16
Q

absence of C1-INH

A

-hereditary angioedema

17
Q

hereditary angioedeme

A
  • rare AD
  • disfunctional C1-INH
  • recurrent episodes of angioedema
  • without urticaria or pruritus, which most often affect the skin and mucous tissue of the upper resp tract
  • laryngeal involvement may cause fatal asphyxiation