mucosal immunology Flashcards

1
Q

general features of immunity at epithelial barriers

A
  • outer epithelial layer to prevent microbial invasion
  • underlying connective tissue containing immune cells that mediate innate immune response and effector arm of adaptive response (lymphocytes, dendritic cells, macrophages, and mast cells)
  • in mucosal tissues: MALT is secondary lymphoid tissue
  • draining lymph nodes where adaptive immune responses are initiated/amplified
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2
Q

regional immune systems

A
  • mucosal immune systems = GI, bronchopulmonary, and GU mucosal barriers
  • cutaneous (skin) immune system
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3
Q

challenges to and special structures/cells of the GI immune system

A

Challenges

  • tolerance of food antigens
  • tolerance of commensal microbiota
  • large SA

Special structures and cells

  • structures: tonsils, peyer’s patches, lamina propria, follicles
  • intestinal epithelial cells secrete mucus
  • M cells sample antigens in lumen
  • Paneth cells make defensins
  • IgA and IgM neutralize bugs
  • dendritic cells sample lumen/lamina propria for antigen, induce T cell tolerance and B cell IgA class switching, activate effector T cells, imprint gut homing phenotype of B and T cells
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4
Q

challenges to and special structures/cells of the respiratory immune system

A

Challenges

  • exposure to airborne pathogenic and innocuous microbes

Structures and cells

  • structures = tonsils, adenoids
  • ciliated respiratory epithelial cells make mucus and defensin and move mucus
  • IgA, IgM, and IgG neutralize microbes
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5
Q

challenges to and special structures/cells or the cutaneous immune system

A

Challenges

  • large SA

Structures/cells

  • structures: keratinizing stratified squamous epithelial barrier
  • keratinocytes make keratin, cytokines, and defensins
  • langerhans cells sample epidermis for antigens
  • dendritic cells sample dermis for antigen, induce T cell tolerance, activate effector T cells, and imprint skin homing T cell phenotype
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6
Q

organization and function of the GI immune system

A

intestinal barrier to microbes:

  • adjacent epithelial cells connected by tight junctions protect lamina propria
  • extensively glycosylated mucin proteins form viscous physical barrier overlying cells of the GI tract
  • mucins can combine with glycolipids to form a protective glycocalyx

innate immune protection

  • defensins produced by intestinal epithelial cells
  • TLR’s and cytoplasmic NLR’s differentiate between pathogenic and commensal
  • dendritic cells and macrophages in the lamina propria inhibit inflammation
  • IL-17 and IL-22 contribute to immune defense; TGF-B, IL-10, and IL-2 maintain homeostasis

adaptive immune protection

  • GALT = subepithelial lymphoid tissues including tonsils and peyer’s patches
  • M cells sample luminal antigens and transport to GALT APC’s
  • humoral immunity = IgA secretion
  • T cell subsets:
  • Th17 secrete IL-17 and IL-22, enhancing epithelial barrier function
  • Th2 involved in parasite defense
  • Tregs suppress inappropriate responses
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7
Q

organization and function of the respiratory immune system

A

Innate immunity

  • physical barrier = pseudostratified columnar epithelium
  • chemical barrier = mucus, defensins, cathelicidins
  • alveolar surfactants (collectins) and alveolar macrophages

Humoral immunity

  • IgA in the upper airway
  • IgE

Cellular immunity

  • T cell response: dendritic cells present antigens to T cells in peribroncial and mediastinal lymph nodes => Th2 cell differentiation
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8
Q

organization and function of the GU immune system

A

Innate

  • epithelial lining = langerhans, dendritic cells, macrophages

Humoral

  • mainly IgG, even though it is mucosal

Cell mediated

  • B and T cells in genital mucosa
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9
Q

organization and function of cutaneous mucosa

A

Innate

  • physical barrier = keratinized squamous epithelial layer
  • chemical barrier = defensins and cytokines secreted by keratinocytes
  • dendritic cells

Cell mediated

  • langerhans cells activated via TLR engagement => express CCR7 chemokine receptor => migrate to T cell zones through the lymphatic vessels
  • CD4+ and CD8+ effector/memory cells; Th1, Th2, and Th17 cells
  • Th17 cytokines (IL-17 and IL-22) => cathelicidins and defensins
  • Th2 cytokines IL-4 and IL-13 suppress defensins and cathelicidins
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10
Q

celiac disease

A

regional mucosa = small bowel mucosa

immune mediators = gluten and transglutaminase 2A specific IgA and IgG, CD4+ T cell responses to gliadin

pathophys = chronic inflammation, malabsorption, nutritional deficiencies

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11
Q

food allergies

A

regional immune system = GI

immune mediators = Th2 dependent IgE response, activation of mast cells

pathophys = inflammation, anaphylaxis, failure of adaptive immune tolerance to food antigens

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12
Q

MALT lymphoma

A

regional immune system = lymphoid follicles in gastric lamina propria

immune mediators = chronic h. pylori infection

pathophys = malignant transformation of B cells

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13
Q

IBD

A

regional immune system = GI (ulcerative colitis is colonic mucosa)

immune mediators = defects in innate immunity to commensals (polymorphisms in related genes), abnormal Th1/Th17, defective Tregs

pathophys = pain, vomiting, diarrhea, weight loss from chronic inflammation

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14
Q

C. diff colitis

A

regional immune system = colon

immune mediators = alteration to normal flora

pathophys = abx alter gut flora => inflammation

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15
Q

chronic rhinosinusitis

A

regional immune systems = nasal/respiratory airway and mucosa

immune mediators = innate defects (barrier, mucus clearance, antimicrobial peptides), abnormal activation of eosinophils/mast cells/innate lymphoid cells, activated T and B cells

pathophys = chroic inflammation => nasal obstruction, drainage, facial pain/pressure

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16
Q

psoriasis

A

regional immune system = cutaneous

immune mediators = dysregulated innate and T cell responses (Th1 and Th17)

pathophys = too much IFN-a, T cells promote inflammatory cascade at dermis => keratinocyte proliferation => red scaly plaques

17
Q

atopic dermatitis (eczema)

A

regional immune system = cutaneous

immune mediators = innate barrier defects, abnormal/increased food or environmental antigen exposure

pathophys = Th2 response in genetically susceptible (B cell production of IgE => mast cell activation)

18
Q

immune privileged sites, mechanisms, and purpose

A

site = brain, anterior chamber of eye, testis

mechanisms = tight junctions, local production of immunosuppressive cytokines, cell surface molecules that inactive or kill lymphocytes

why = high risk of lethal organ dysfunction or reproductive failure in the event of an immune response