6A: Immune system & Infection Flashcards

1
Q

Microbial factors

A
  • Type of organism (e.g. virus, bacterium, parasite)
  • Dose (degree of exposure)
  • Virulence
  • Route of entry
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2
Q

Host factors

A
  • Integrity of innate barriers
  • Adaptive immune competence
  • HLA, Ig & TCR genes
  • Previous exposure
  • Other infections
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3
Q

Viruses

A
  • Lytic or integrated cycle
  • Capsid antigens
  • Internal structural components (HLA)
  • Metabolic products (HLA)
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4
Q

Bacteria (& fungi)

A
  • Extracellular (e.g. S. aureus) or intracellular (e.g. M. tuberculosis)
  • Structural components
  • Metabolic products & toxins
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5
Q

Parasites

A
  • Large (multicellular) (slower)
  • Life cycle changes
  • Radical changes in antigenicity
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6
Q

Antibody structure

A
  • 2 light chains
  • 2 heavy chains joined with disulphide bonds at hinge region
  • Hypervariable regions on light chains
  • Complement-binding region
  • Fc region (links to receptors)
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7
Q

5 classes of antibodies

A
  1. IgM – first in primary response, large, mostly in bloodstream
  2. IgG – second in primary response, dominates secondary response, most abundant, in most body fluids
  3. IgA – high in mucus, surface protection
  4. IgE – associated with basophils & mast cells, allergies, (parasites)
  5. IgD – surface reception of naïve antigen-sensitive B cells
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8
Q

Cytotoxic T lymphocytes

A
  • Viral peptide is presented by HLA class I

- Cytotoxic T cell recognises HLA class I & binds, killing the target cell

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9
Q

Immune factors

A
  • Direct neutralisation by antibodies
  • Opsonisation & phagocytosis
  • Complement-mediated effects
  • HLA-restricted T cell-mediated cytotoxicity
  • NK cell-mediated cytotoxicity
  • Inflammatory & regulatory cytokines
  • Antiviral cytokines (e.g. interferons)
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10
Q

Antibodies: Effective against antigens outside cells of body

A
  • Viruses (IgA, IgG, IgM)
  • Toxins (IgG, IgM)
  • Extracellular bacteria (IgA, IgM, IgG)
  • Parasites (IgE, IgA)
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11
Q

Cytotoxic T cells: Effective against intracellular protein antigens

A
  • Virus infections (cytoplasmic peptides)
  • Tumour cells
  • Transplanted organs
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12
Q

Immunity to bacteria

A

Antibodies & complement:

  • Enhance bacterial destruction
  • Enhance phagocytosis (opsonisation)

Bacterial resistance:
- Capsule resists opsonisation (e.g. Haemophilus influenzae)
+ Slippery capsule of Haemophilus influenza avoids them being eaten by neutrophils
- Intracellular growth

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13
Q

Antibodies around birth

A
  • When utero baby has maternal antibodies (IgG)

- After birth maternal antibodies decrease and Childs own antibodies develops

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14
Q

Interferon antiviral mechanism

A
  • Interferons send signals from virus infected cells to uninfected cells so the uninfected cells can protect themselves from the virus
  • Interferons activate Natural Killer cells to seek out & kill virus cells more effectively
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15
Q

Cytokines in infection

A
Proinflammatory (IL-1, IL-6, TNF-a)
- Early, induce acute phase proteins
- Temperature (fever) & behavioural changes
- TNF-a triggered by bacterial LPS
- Tissue repair:
\+ Bone resorption
\+ Fibroblast proliferation
\+ Collagenase synthesis
\+ Leukocyte adhesion
- T & B cell activation

Chemokines:

  • Aid chemotaxis (e.g. neutrophils)
  • Direct effector cell traffic

Interferons:

  • Induce transient antiviral state
  • Activate NK cell activity
  • Upregulate HLA expression (improves cytotoxic T cell killing)
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16
Q

Result of hygienic environment

A

Different infections + Different antigens lead to:

  • Different profile of immune responses
  • More allergies & hypersensitvities
  • More inflammatory diseases & autoimmune diseases
17
Q

Vaccines

A

Whole live organisms: E.g. Cowpox, measures, mumps, rubella, BCG

  • Established infection in vaccinated person
  • Immune responses clear infection after 1-2 weeks
  • Prolonged exposure to organism
  • Single dose usually effective at stimulating lifelong immunity

Whole killed organisms or components or organisms: E.g. pertussis, hepatitis B, tetanus, Haemophilus influenzae

  • Briefly expose vaccinated persons to antigens of organism
  • Immune response clear antigens within a few days
  • Three (or more) doses to stimulate good immunity
18
Q

Polysaccharide vaccines

A
  • Streptococcus pneumonia (23-valent)
  • Meningococcus
  • Typhoid
  • Very weak antibody response to polysaccharide antigens
  • Little immunological memory
  • Conjugate vaccine developed
19
Q

Conjugate vaccines

A
  • Polysaccharide attached to a carrier protein
  • Taken up by B cells
  • Protein digested & antigen presented to provide help
  • T cells stimulated to provide help
  • Converts into a T cell dependent antigen
  • Good immunogenicity