Intro to Host Defense Flashcards

1
Q

3 external immune mechanisms

A
  1. Special anatomical structures
  2. Behavioral adaptations
  3. Reproductive bursts
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2
Q

3 internal immune mechanisms

A
  1. Dealing with invading pathogens
  2. Removing worn-out cells
  3. Identify and remove abnormal or mutant cells
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3
Q

Primary cellular elements of adaptive immunity

A

T & B lymphocytes

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4
Q

3 functions of acquired immunity

A
  1. Specific recognition of foreign antigens
  2. Immunological memory of infection
  3. Pathogen-specific adaptor proteins
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5
Q

3 bad things that come from acquired immunity

A
  1. Allergies
  2. Autoimmunity
  3. Tissue graft rejection
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6
Q

Innate immune system distinguishes between?

A

“Infectious non-self” and “non-infectious self”

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7
Q

3 cells which trigger innate immunity (via inflammatory responses mainly)

Via what receptors?

A
  1. Neutrophils
  2. Macrophages
  3. Mast cells

Via host defense surveillance receptors

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8
Q

Adaptive immune response is generally mediated by the same cells used for innate immunity, but in what different way?

A

Molecularly-specific receptor systems

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9
Q

Innate immune mechanisms are abundant in what tissue?

A

Barrier tissues:

  1. Skin
  2. Epithelial tissues of gut and respiratory
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10
Q

Innate immune mechanisms delay need for acquired immune response how and for how long?

A

3-5 days for clonal expansion and differentation of effector lymphocytes

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11
Q

General mechanisms of innate immunity

A
  1. Barrier tissue and glands
  2. Inflammation
  3. Complement system
  4. Interferons (antiviral effector proteins)
  5. NK cells
  6. Symbiotic bacteria (“natural flora”)
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12
Q

How does epidermis contribute to innate immunity?

A
  1. Keratinized epithelial cells form physical barrier and chemically detoxifies potential carcinogens
  2. Melanocytes absorb UV light
  3. Keratinocytes are immune-sensing
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13
Q

How does dermis contribute to innate immunity?

A
  1. Sweat and sebaceous glands secrete antimicrobial peptides

2. Abundant blood vessels participate in inflammation

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14
Q

How does genitourinary system contribute to innate immunity?

A
  1. Mucus
  2. High salt
  3. Low pH
  4. Normal flora
  5. Antimicrobial peptides
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15
Q

How does respiratory tract contribute to innate immunity?

A
  1. Filtering mechanisms in nasal passages
  2. Mucus
  3. Cilia (mucus escalator)
  4. Alveolar macrophages
  5. Antimicrobial peptides (in upper and lower respiratory tract)
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16
Q

How does GI tract contribute to innate immunity?

A
  1. Paneth cells (epithelial cells in upper GI which produce antimicrobial peptides)
  2. Lysozyme in saliva
  3. Gastric acid
  4. Commensal flora in upper GI, rumen and/or large intestine
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17
Q

Paneth cells

A

Epithelial cells in upper GI which produce antimicrobial peptides

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18
Q

Classic signs of inflammation

A
  1. Tumor (swelling)
  2. Rubor (redness)
  3. Calor (heat)
  4. Dolor (pain)
  5. Loss of function
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19
Q

Rubor

20
Q

Calor

21
Q

Dolar

22
Q

Goals of inflammatory response

A
  1. Isolate, destroy and/or inactive invaders
  2. Remove debris
  3. Prepare tissue for healing and repair
23
Q

Histamine functions

A
  1. Increase local blood flow → increases delivery of inflammatory cells and mediators
  2. Increase capillary permeability to deliver inflammatory mediators to extracellular space
24
Q

Mast cells are resident in tissue and do what functions:

A
  1. Release histamine

2. Release cytokines

25
Cytokines
Attrach other inflammatory cells (macrophages and neutrophils)
26
Localized edema arises from?
1. Increased colloid osmotic pressure in extracellular space 2. Increased capillary blood flow 3. Increased capillary permeability
27
How does localized edema contribute to pain?
Distends tissue
28
What is inflammation (in a very micro sense)
Leaked plasma in interstitial space clots
29
Locations of pattern recognition receptors
1. Cell surfaces 2. Intracellular compartments 3. Secreted into bloodstream and tissue fluids
30
Principal specific functions of pattern recognition receptors
1. Opsonization 2. Activation of complement and coagulation pathways 3. Phagocytosis 4. Activation of proinflammatory signaling pathways 3. Apoptosis induction
31
Acute-phase proteins are produced by?
Liver during early stages of infection and inflammation
32
Acute-phase secreted pattern recognition proteins
1. Mannan-binding lectin (MBL) 2. Serum amyloid protein (SAP) 3. C-reactive protein (CRP)
33
2 proteins that can function as opsonins
1. CRP | 2. SAP
34
How do CRP and SAP function as opsonins?
Binding to phosphatidylcholine on bacterial cell surfaces
35
In addition to acting as opsonins, CRP and SAP can also do what?
Initiate classical complement pathway
36
What does MBL do?
1. Bind to terminal mannose residues on microbial surfaces | 2. Associates with complement-initiating serine protease
37
Why is there a need for intracellular pattern recognition proeins?
Viruses and some bacterial pathogens can gain access to intracellular compartments like cytosol
38
Protein kinase R (PKR) function
Binds to and is activated by dsRNA (produced during viral infection) → inactivates eIF2 via phosphorylation
39
Muramyl dipeptide (MDP)
Bacterial cell wall component → binds to and activates NOD2 (nucleotide-binding oligomerization domain)
40
TLR4 (toll-like receptor 4) KNOW ME
Recognies LPS
41
LPS
Lipopolysaccharide → component of bacterial cell walls (mainly gram-neg) which induces powerful inflammatory responses, shock and death
42
TLR2 recognizes:
1. Bacterial cell-wall peptidoglycan 2. Bacterial lipoproteins 3. Some LPSs 4. Glycophosphotidylinositol from T. cruzi 5. Yeast cell wall zymosan
43
TLR5 (KNOW THIS)
Recognizes flagelin
44
Flagellin
Protein found in bacterial flagellae (on cell surface)
45
TLR9
Recognizes unmethylated CpG motifs present in bacterial or viral DNA
46
How do TLRs signal?
Via pathogen-associated molecular patterns (PAMPs)
47
MyD88
PAMP receptor → causes inflammation, costimulation and antimicrobial genes