Immunology Flashcards

1
Q

what mediates type 1 hypersensitivity reactions

A

IgE

- allergy

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2
Q

what mediates type 2 hypersensitivity reactions

A

Complement (IgG or IgM)

  • cytotoxic
  • antibody dependent
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3
Q

what mediates type 3 hypersensitivity reactions

A

IgG complement, neutrophils

- immune complex mediated

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4
Q

what mediates type 4 hypersensitivity reactions

A

T cells

- delayed hypersensitivity

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5
Q

what type of reaction are eczema, hives and hay fever

A

type one

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6
Q

what type of reaction is SLE

A

Type 3

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7
Q

what type of reaction is ABO mismatch

A

Type 2

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8
Q

what type of reaction is RA

A

Type 3

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9
Q

what type of reaction is contact dermatitis

A

Type 4

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10
Q

what type of reaction is a graft rejection

A

Type 4

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11
Q

primary lymphoid tissue

A

bone marrow + thymus

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12
Q

secondary lymphoid tissue

A

spleen + tonsils

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13
Q

proteins in innate immune system

A

complement
acute phase proteins
cytokines

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14
Q

proteins in adaptive immune system

A

antibodies

cytokines

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15
Q

leukocytes in adaptive immune system

A

B lymphocytes

T lymphocytes

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16
Q

leukocytes in innate immune system

A
macrophage 
neutrophils 
dendritic cells 
basophils 
eosinophils 
NK cells
17
Q

opsonins that enhance phagocytosis

A

C3b
collectins
CRP

18
Q

interferons

A

anti-viral activity

19
Q

TNF alpha

A

pro- inflammatory cytokine

20
Q

what interleukin activates CD8 T cells

A

IL 2

21
Q

antibody found in breast milk, saliva, tears

A

IgA

22
Q

antibody that provide maternal immunity

A

IgG

23
Q

first antibody produced in acute infection

A

IgM

24
Q

what does MHC 1 present to

A

CD8 T cells

25
Q

what does MHC 2 present to

A

CD4 T cells

26
Q

what is deficient in chronic granulomatous disease

what are the symptoms

A

NADPH oxidase - failure of oxidative killing

- recurrent pneumonias + abscesses

27
Q

what is the most common primary antibody deficiency

A

selective IgA deficiency

28
Q

features of selective IgA deficiency

A

recurrent sinus + resp infections

associated with coeliac disease

29
Q

features of X linked (Burtons) congenital agammaglobulinaemia

A

recurrent bacterial infections

  • absent B cells
  • reduction in ALL immunoglobulins
30
Q

features of severe combined immunodeficiency

A

X linked

  • recurrent VIRAL, BACTERIAL + FUNGAL infections
  • failure to produce lymphocytes
  • IL2 mutation
  • presents after 3 months of life- diarrhoea, failure to thrive
31
Q

features of common variable immunodeficiency

A

low serum immunoglobulins
increase in ENT + resp infections
presents in 30-40s

32
Q

what cells form a granuloma

A

macrophage + lymphocytes

33
Q

what cells kill virally infected cells

A

NK cells

cytotoxic T cells

34
Q

what receptors recognise pathogens

A

toll like receptors
lectin receptors
scavenger receptors

35
Q

leukocyte adhesion deficiency

A

neutrophils fail to bind to endothelial markers
decent in CD18
Increase neutrophil count during infection