Lecture 12- Mucosal Immunology 1 Flashcards

1
Q

What is MALT,BALT and GALT?

A

MALT:The mucosa-associated lymphatic tissue is divided into:
BALT (bronchus-associated lymphatic tissue)
and
GALT (gut -associated lymphatic tissue)

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2
Q

Why is the mucosal immune system imprtant?

A
  • Biggest immune compartment of the organism
  • Harbours 60% of all effector cells
  • Direct contact with the outside environment
  • continuous antigen stimulation- food, endogenous flora and pathogens
  • muscosal sites are entry for many infections
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3
Q

What are the main defence strategies of intestinal muscosa and oropharynx?

A

1) Endogenous flora
2) Epithelium and mucus:
- Mechanical barriers (cells and tight junctions)
- mucins: extensively glycosylated proteins from a viscous barrier
- specialised epithelial cells (goblet cells, M cells, paneth cell)
- Antimicrobial substances (defensins, lysozymes, lactoferrins and phospholipases)
3) Regionalised immune systems and gut homing of B and T cells
- Waldeyer’s ring ( lingual and palatine tonsils, nasopharyngeal tonsils)
- Peyers patch
- Mesenteric lymph nodes
- Intraepithelial immune cells
- Lamina propria immune cells including sampling DC

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4
Q

Describe the lymphoid complexes that are found along the GI tract?

A

The largest amount of lymphoid tissue is found in the oropharynx (waldeyer’s ring) and the terminal ileum

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5
Q

what is a major factor in maintaining a healthy composition of microorganism in the gut?

A

Diet is a major factor in maintaining a healthy composition

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6
Q

How does goblet cells improve host’s defence?

A

Goblet cells produce mucus- physio chemical barrier

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7
Q

what are other special properties of the intestinal epithelial cells for improving hosts defence?

A

Epithelial cells express TLR

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8
Q

Which TLR is expressed on the basolateral surface and what activates it?

A

TLR5- invading bacteria

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9
Q

When are the NRL located?

A

Intracytoplasmic

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10
Q

What are the NRL activated by and how?

A

Bacterial flagellin once bacteria entr the cytoplasm

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11
Q

What’s the other functions of the surface TLR ligation

A

-TLR ligation will:
1) cause tightening of epithelial junctions
2)Increase proliferation
3)Epithelial motility
All improve barrier function

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12
Q

what is the purpose of the M cells?

A

-transport antigens to sub-epithelial lymphoid structure

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13
Q

What is the function of paneth cells?

A

Paneth cells produce human defensin 5 precursor (HD5) HD6 precursor and trypsin

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14
Q

What is the function of trypsin?

A

Activation of HD5 and HD6 by proteolytic cleavage

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15
Q

Describe what peyers patches are located ?

A

-Located in the distal ileum areas of the follicle associated epithelium

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16
Q

Compare the peyers patches in the foetus at 30 weeks compared to at puberty?

A

Foetal human small intestine contains average of 60 peyers patch before the age of 30 weeks
-At puberty max of 240

17
Q

what does the peyers patch contain?

A
  • Peyers patch contain germinal centres for B and T cells

- Inductive site for immune response

18
Q

Describe the features of M cells?

A
  • Small microvilli
  • Large cell membrane fenestration: these features enhance antigen uptake from the gut lumen
  • Trans-cellular transport of antigen
  • Exocytosis at basolateral membrane
  • Delivery of dendritic cells in some region of underlying lymphatic structure
19
Q

Describe the three main domains of peyers patches?

A
  • The follicular area
  • The interfollicular area
  • Follicle-associated epithelium
20
Q

What does the follicular and the interfollicular areas contain?

A

Have lymphoid follicles with a germinal centre contains:

  • proliferating B cells
  • Follicular dendritic cells
  • macrophages
21
Q

What is the follicle surrounded by?

A

Follicle is surrounded by:
-Corona
-subepithelial dome
:these contain mixed cellsincluding B cells, T cells, macrophages and dendritic cells.

22
Q

How does Follicular associated epithelium (FAE) differs from normal epithelium?

A

FAE differd in regards to microvilli regularity and length and presence of infiltrating immune cells

23
Q

how is peyers patches connected to the blood supply and lymphatic system?

A

Blood supply- endothelial vessels

-Peyers patch to mesenteric lymph node

24
Q

How does the naive B cells enter the peyers patch?

A

-Specialised high endothelial venules

25
Q

What is the result of B cells entering?

A

If they recognise the antigen coming in from he M cell at the top of Peyers patch, they get activated and start proliferating

26
Q

which other cell enter the peyers patch via high endothelial venules and happens to them?

A
  • Naive CD4 Tcells also enter peyers patch via the high endothelial venules
  • If they encounter a dendritic cell presenting antigen to them that they recognise
  • They proliferate and increase in number
  • Some of CD4 cells may then encounter B cells activated by the same antigen
27
Q

When does the B cells class switch?

A

When T cell/B cell help takes place: they activate each other, T cells move onto to become mature cells and B cells under Immunoglobulin class switch into plasma cells

28
Q

what happens to the activated B cells and T cells in the pyeres patch?

A

Most activated T cells and B cells both leave the peyers patch via the lymphatic drainage and reach their destination via the blood

29
Q

what is the most special influence of peyers patch on B cells what is required for this to occur?

A

Peyers patch program B cells to produce IgA- This occurs in the influence of nitric oxide and TGF beta from dendritic cells.