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

21
Q

antibody found in breast milk, saliva, tears

22
Q

antibody that provide maternal immunity

23
Q

first antibody produced in acute infection

24
Q

what does MHC 1 present to

A

CD8 T cells

25
what does MHC 2 present to
CD4 T cells
26
what is deficient in chronic granulomatous disease | what are the symptoms
NADPH oxidase - failure of oxidative killing | - recurrent pneumonias + abscesses
27
what is the most common primary antibody deficiency
selective IgA deficiency
28
features of selective IgA deficiency
recurrent sinus + resp infections | associated with coeliac disease
29
features of X linked (Burtons) congenital agammaglobulinaemia
recurrent bacterial infections - absent B cells - reduction in ALL immunoglobulins
30
features of severe combined immunodeficiency
X linked - recurrent VIRAL, BACTERIAL + FUNGAL infections - failure to produce lymphocytes - IL2 mutation - presents after 3 months of life- diarrhoea, failure to thrive
31
features of common variable immunodeficiency
low serum immunoglobulins increase in ENT + resp infections presents in 30-40s
32
what cells form a granuloma
macrophage + lymphocytes
33
what cells kill virally infected cells
NK cells | cytotoxic T cells
34
what receptors recognise pathogens
toll like receptors lectin receptors scavenger receptors
35
leukocyte adhesion deficiency
neutrophils fail to bind to endothelial markers decent in CD18 Increase neutrophil count during infection