Immunology 1 Flashcards

1
Q

Define pathogen

A

A microorganism that causes disease when it infects a host

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2
Q

Define zygomen

A

Inactive form of an enzyme, usually protease. Modified to become active

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3
Q

Define chemokine

A

A small chemoattractant protein that stimulates the migration and activation of cells

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4
Q

Define cytokine

A

A small protein affecting behaviour of other cells - if secreted by lymphocytes, they’re called interleukins

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5
Q

What are the layers of defence as the pathogen attacks

A

Layer 1 - Physical (skin, hair)
Layer 2 - Soluble factors (breathe in)
Layer 3 - Innate arm (first response to pathogen)
Layer 4 - Adaptive arm (secondary response)

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6
Q

What barriers to infection do surface epithelia provide (layer 1 - physical)

A
  • Mechanical
  • Chemical
  • Microbiological
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7
Q

Describe layer 2 (soluble factors)

A
  • Bacterial walls contain peptidoglycan (polymer of 2 sugars)
  • Lysozymes in saliva are most active against gram +ve bacteria as they break the beta 1-4 glycosidic bond - exposes lipid bilayer of bacterial membrane to other antimicrobial agents
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8
Q

What are defensins?

What do defensins do?

A
  • Short, cationic peptides
  • Insert into membrane and generate pores so membrane becomes leaky
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9
Q

What are cathelicidins?

What do cathelicidins do?

A
  • Peptides that don’t contain disulphide bonds
  • In neutrophils, they’re only activated when needed
  • Amphipathic
  • Carboxy-terminal peptide disrupts membrane
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10
Q

What are histatins?

What do histatins do?

A
  • Peptides produced by parotid, submandibular and sublingual salivary glands
  • Active against pathogenic fungi (e.g. yeast)
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11
Q

What is the difference between the innate arm and adaptive arm in terms of:
- Response speed
- Recognition of self (host) and non-self (pathogen)
- Lasting protection/memory

A
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12
Q

What are the stages of the compliment system

A
  1. Activation occurs on surfaces e.g. bacterium surface
  2. Pattern recognition receptors of antibodies detect the antigen pathogen
  3. Antibodies activate the initial zymogen
  4. Creates a cascade of proteolysis where complement zymogens become proteolytically cleaved + activate many molecules of the next zymogen in the pathway
  5. Therefore, even if small numbers of pathogens are detected, a rapid response is produced
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