mucosal immunity

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29 Terms

1
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Which organs are part of the mucosal immune system?

GI tract, respiratory tract, urogenital tract, eyes, mouth, salivary glands, mammary glands.

2
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Why is the mucosal immune system unique?

Constant exposure to microbes + huge surface area.

3
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What is mucus made of?

Mucins (glycoproteins) from goblet cells.

4
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Why is mucus important?

Traps microbes, lubricates surfaces, forms protective barrier; varies in properties across tissues.

5
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What are key functions of gut microbiota?

Make vitamins (e.g., K), digest polysaccharides, detoxify substances, outcompete pathogens, help develop MALT/GALT.

6
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What do germ-free mice show?

Underdeveloped mucosal + systemic immunity; demonstrates microbiota is essential.

7
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How can commensals be dangerous?

Overgrowth → infections (E. coli, Salmonella, Shigella, Helicobacter).

8
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Why is the mucosal immune system “proactive”?

Constantly produces IgA, mucus, and effector cells.

9
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Why is it “tolerant”?

Avoids inflammation to prevent epithelial damage.

10
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What happens if tolerance fails?

IBD, celiac disease.

11
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What is the inductive compartment?

Where antigen is presented to activate lymphocytes (e.g., Peyer’s patches, ILFs).

12
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What is the effector compartment?

Contains effector T cells, plasma cells, macrophages, etc., in epithelium + lamina propria.

13
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Examples of inductive tissue?

Peyer’s patches, isolated lymphoid follicles (ILFs).

14
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Examples of effector sites?

Intraepithelial space + lamina propria.

15
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What receptors do gut epithelial cells express?

TLRs (apical/basolateral), NOD proteins (cytoplasm).

16
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What do these receptors activate?

NF-κB → antimicrobial peptides, chemokines, cytokines, defensins.

17
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What type of macrophages dominate in the gut?

M2 (tolerant, non-inflammatory).

18
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Key features of gut macrophages?

Strong phagocytes but no inflammatory cytokines, no respiratory burst, no B7.

19
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How is antigen sampled in the gut?

M cells in Peyer’s patches transcytose lumen contents into the intraepithelial pocket for DCs/T/B cells.

20
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Types of gut DCs?

In Peyer’s patches + lamina propria; some extend dendrites into lumen.

21
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What is oral tolerance?

Food antigens induce tolerance, not inflammation; mediated by CD103⁺ DCs → Tregs.

22
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How do DCs respond to commensals?

Activate Tfh cells → promote secretory IgA production.

23
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Where are lymphocytes found?

Peyer’s patches, ILFs, lamina propria, epithelium.

24
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What do gut-homing lymphocytes express?

CCR9 (binds CCL25) + α4β7 integrin (binds MAdCAM-1).

25
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What are IELs (intraepithelial lymphocytes)?

IELs are a unique population of lymphocytes that reside within the epithelial lining of various tissues, most notably the gastrointestinal tract. They are primarily T cells (both \alpha\beta and \gamma\delta T cells) that play a critical role in immune surveillance, maintaining epithelial barrier

26
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How is sIgA produced?

B cells activated in GALT → IgM → switch to dimeric IgA.

27
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Role of sIgA?

Neutralizes microbes, traps them in mucus, prevents epithelial attachment.

28
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What happens to T/B cells activated in MALT/GALT?

Gain integrin α4β7, lose CCR7 and L-selectin → home to mucosal tissues.

29
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Can activated cells migrate to other mucosal sites?

Yes, activated cells acquire specific homing receptors (e.g., \alpha4\beta7 integrin and CCR9) that direct them to other mucosal sites.