Complement Flashcards

1
Q

Complement pathway activated by antigen-antibody complexes (IgG or IgM)

A

Classical pathway

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2
Q

Complement pathway activated by microbe surface molecules

A

Alternative pathway

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3
Q

Complement pathway activated by mannose or sugars on microbes

A

Lectin pathway

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4
Q

Complement protein involved in opsonization

A

C3b

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5
Q

Complement proteins involved in anaphylaxis

A

C3a, C4a, C5a

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6
Q

Complement protein involved in neutrophil chemotaxis

A

C5a

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7
Q

Complement complex responsible for cytolysis

A

MAC (C5b-9)

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8
Q

Two main opsonins in bacterial defense

A

C3b and IgG

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9
Q

Proteins that prevent complement activation on self cells

A

DAF (CD55) and C1 esterase inhibitor

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10
Q

Deficiency of early complement proteins (C1-C4) increases risk of

A

SLE and recurrent infections

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11
Q

Deficiency of terminal complement proteins (C5-C9) increases susceptibility to

A

Neisseria infections

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12
Q

Deficiency causing hereditary angioedema due to ↑ bradykinin

A

C1 esterase inhibitor deficiency

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13
Q

Disorder caused by impaired GPI anchor synthesis, leading to complement-mediated lysis of RBCs

A

Paroxysmal nocturnal hemoglobinuria

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14
Q

Complement pathway activated by antigen-antibody complexes (IgG or IgM)

A

Classical pathway

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15
Q

Complement pathway activated by microbe surface molecules

A

Alternative pathway

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16
Q

Complement pathway activated by mannose or sugars on microbes

A

Lectin pathway

17
Q

Complement protein involved in opsonization

18
Q

Complement proteins involved in anaphylaxis

A

C3a, C4a, C5a

19
Q

Complement protein involved in neutrophil chemotaxis

20
Q

Complement complex responsible for cytolysis

A

MAC (C5b-9)

21
Q

Two main opsonins in bacterial defense

A

C3b and IgG

22
Q

Proteins that prevent complement activation on self cells

A

DAF (CD55) and C1 esterase inhibitor

23
Q

Deficiency of early complement proteins (C1-C4) increases risk of

A

SLE and recurrent infections

24
Q

Deficiency of terminal complement proteins (C5-C9) increases susceptibility to

A

Neisseria infections

25
Q

Deficiency causing hereditary angioedema due to ↑ bradykinin

A

C1 esterase inhibitor deficiency

26
Q

Disorder caused by impaired GPI anchor synthesis, leading to complement-mediated lysis of RBCs

A

Paroxysmal nocturnal hemoglobinuria