Immunity Flashcards

1
Q

Muscosa is vulnerable due to

A

Fragility and permeability

Requires effective defence mechanisms, portals of entry for non-pathogenic anitgens

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2
Q

Intestinal lymphocytes are found

A
  1. In organised tissues where immune responses are induced

2. Scattered throughout intestine where they carry out effector functions

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3
Q

Peyer’s patches are found

A

in the small intestine

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4
Q

Peyer’s patches are covered by an epithelial layer containing

A

Specialised M cells

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5
Q

Characteristic of M cells

A

Ruffles

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6
Q

How do M cells work

A

Take up antigen by endocytosis and transport to dendritic cell which activates T cells

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7
Q

Adaptation of dendritic cells

A

Can reach through epithelial layer to capture antigen from lumen

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8
Q

2 compartments of mucosal immune system

A
  1. Immune cells of lamina propria

2. Immune cells of epithelial layer

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9
Q

T cells enter Peyer’s patch from

A

blood vessels

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10
Q

How do T cells in Peyer’s patch work

A

When activated, they drain through lymph nodes to thoracic duct and return to gut via bloodstream

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11
Q

Paneth cells secrete

A

Defensins

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12
Q

Where are Paneth cells found

A

SI not large

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13
Q

IgA in GI tract

A

80%

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14
Q

IgM in GI tract

A

15%

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15
Q

IgG in GI tract

A

5%

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16
Q

IgA

A

Can neutralise pathogens and toxins

17
Q

IgA internalised in endosomes

A

Export toxins and pathogens from lamina propria while being secreted

18
Q

Special T cells in gut

A

IEL’s

Intraepithelial lymphocytes

19
Q

IEL’s

A

80% CD8+

  1. Virus infects mucosal epithelium cell
  2. Activated IEL kills epithelial cell by Fas dependant pathway
20
Q

Infectious disease

A

Infection crosses mucosa and fuses to dendritic cells which shuttle virus to lymph nodes
Infection spreads to CD4+ lymphocytes
Viral infected cells go into bloodstream and disseminate across body

21
Q

Primary Immunodeficiency

A
Selective IgA deficiency
CVID
XLA
CGD
SCID
22
Q

Selective IgA deficiency

A

Aysmptomatic

Recurrent sino-pulmonary infection (coeliac disease X10)

23
Q

Common Variable Immunodeficiency

A

Recurrent sino-puomonary and GI infections (low IgM+G)

24
Q

X linked Agammaglobulinaemia

A

Sino-pulmonary and GI infetcions

Devastating entervoviral infection (no B cells)

25
Q

Chronic Granulomatous disease

A

Staph aureus/inflammatory granulomas

Abscesses

26
Q

Severe combines immunodeficiency

A

Defect in T and B cell immunity

Oral candidas, rotavirus, EBV

27
Q

Allergy

A

IgE secreted by plasma cells binds to mast cells
Secrete signals to B cells
Stimulates further IgE production

28
Q

Common allergens

A

Drugs, serum, venom and food (peanuts)

29
Q

Crohn’s

A
Mediated by Th1 CD4+ T cells
Gamma inteferon
IL-12
TNF alpha
Gene = NOD2
30
Q

UC

A

May be NK T cell mediated via IL-13