Host Defense Mechanisms of the Lung Flashcards

1
Q

upper airway and bronchi defense?

A
anatomic barriers
cough
mucociliary apparatus
airway epithelium
secretory IgA
dendritic cells, lymphocytes, and neutrophils
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2
Q

alveolar space defense?

A

alveolar macrophage
immunoglobulins, opsonins, surfactants
lymphocyte mediated immunity
neutrophils and eosinophils

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3
Q

greater than 10 microns?

A

tonsils and adenoids

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4
Q

2-10 microns?

A

mucokinesis and coughing

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5
Q

less than 2 microns?

A

alveolar macrophages

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6
Q

cough reflex?

A

deep inspired
shut off air (close glottis)
expiratory effort, builds pressure
release high pressure trapped air

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7
Q

airway epithelial cells?

A

barrier function

  • release bacterostatic molecules
  • regulation of immune response

secrete IgA

**toll like receptors

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8
Q

secretory IgA

A

produced by plasma cells

  • heterodimer
  • secreted into lumen

**important for defense at mucosal surfaces

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9
Q

dendritic cells

A

trap antigen and present to other cells in lymphoid strictures

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10
Q

BALT

A

bronchial associated lymphoid tissue

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11
Q

GALT

A

gut associated lymphoid tissue

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12
Q

mucociliary clearance

A

2-10 microns deposited on mucus of upper airways

altered in asthma, chronic bronchitis, and cystic fibrosis

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13
Q

mucus contains?

A

IgA, lysozyme, lactoferrin, peroxidase

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14
Q

gel-on-brush model

A

propose model for mucus clearance

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15
Q

cystic fibrosis

A

mutant in CFTR gene
-cystic fibrosis transmembrane conductance regulator

-prevents chloride transport out of cell (Cl- and Na+ abnormalities)

accumulation of thick and viscous mucus - difficult to move it out (it is actually dehydrated)

increased risk of infecton

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16
Q

mucus in cystic fibrosis?

A

dehydrated**

normal - Kmucus less than Kpcl
dehydrated - Kmucus equals Kpcl

17
Q

common pathogens in cystic fibrosis?

A

pseduomonas aeruginosa
burkholderia cepacia
staphylococcus aureus
haemophilus influenza

18
Q

CFTR gene mutations?

A

pathogens can embed in mucus and survive in these suitable microenvironments

19
Q

defense in alveoli?

A

IgA and IgG
surfactant, fibronectin, C reactive protein
lymphocyte antibody production
neutros and eosinos

20
Q

protease/antiprotease in respiratory system?

A

neutrophil elastase
metalloproteinase
alpha-1 antitrypsin

imbalance can cause problems

21
Q

epithelial cell recognition of pathogens?

A

ligation of toll like receptors

recognize flagellin, LP5, etc.

22
Q

innate immune response?

A

dendritic cells
neutrophils
NK cells

23
Q

adaptive immune response?

A

effector T cells

24
Q

pathology of pneumonia?

A

lung inflammation associated with alveoli filling in response to lung infection

25
Q

predisposing factors of pneumonia?

A

age - increases with age
immune status - immuno compromised
presence of lung disease - CF, chronic bronchitis

26
Q

pneumonia?

A

V/Q mismatch

  • vasoconstriction in edematous areas
  • will develop hypoxemia
  • CO2 levels should be fine
  • pain with chest wall movement
27
Q

no change amines?

A

dopamine
adrenaline
histamine

28
Q

inactivated amines?

A

5-hydroxytryptamine

noradrenaline

29
Q

activated peptide?

A

ANG I

-converted to ANG II in lung**

30
Q

no change peptides?

A

ANG II
oxytocin
vasopresin

31
Q

ANG 1 - 2

A

in lung**

32
Q

inactivated peptides?

A

bradykinin
ANP
endothelins

33
Q

activated arachidonic acid derivatives?

A

arachidonic acid

34
Q

no change arachidonic acid derivative?

A

PGI2

PGA2

35
Q

Inactivated arachidonic acid derivative?

A

PGD2, PGE2, PGF2a

36
Q

inactivated purine derivatives

A
leukotrienes
adenosine
ATP
ADP
AMP