Vaccines 1 Flashcards

1
Q

What should you consider before vaccinating an animal?

A
  • Pathogen and protective immune response
  • Age/ colostrol Ab decline
  • Immunosenescence (gradual decline of immune system with age)
  • Health (immunodeficiency?)
  • Management (individual or herd?)
  • Pregnancy status
  • Vaccine efficacy (how long it lasts)
  • Adverse effects/ risks
  • Route of administration and impact (e.g. beef carcass)
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2
Q

Describe passive immunisation

A
  • Colostrum (protect against local pathogens) given orally to foals with low IgG within 24-36hrs of birth
  • Serum or purified Ig: donor animals are hyper immunised against specific pathogen. Their serum or Ig is then purified and given to deficient animals
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3
Q

What are the dangers of giving antibody rich serum?

A
  • Can get serum sickness

- Immune complex disease (type 3 hypersensitivity)

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4
Q

What are the basic characteristics of active immunisation?

A
  • Repeated immunisation with vaccine
  • Commonly with adjuvants
  • Induces long term immunity
  • Memory cell formed
  • Multiple route of administration
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5
Q

What are the different routes of administration for active immunisation?

A
  • Systemic: IM (avoid adverse effects of adjuvants), subcut, intradermal
  • Mucosal (common): aerosol, intranasal
  • Water
  • In ovo
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6
Q

Describe mucosal vaccination

A
  • Given locally to site of pathogen invasion
  • Immunity tends to be shrot lives (weeks)
  • Can be used in combination e.g. equine influenza you give an IM injection the booster it with mucosal vacc
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7
Q

Give examples of some mucosal vaccs

A
  • Oral: salmonella
  • Intranasal: KC, feline calicivirus, Bovine IBR
  • Aerosol: Newcastle disease in chickens
  • Immersion (gills/ oral uptake in fish)
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8
Q

Describe different adjuvants used in vaccs

A
  • Aluminium and calcium salts (very safe)
  • Microbial products
  • Synthetic agents
  • Exogenous cytokines
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9
Q

How do adjuvants help?

A
  • They non specifically enhance Th2 response in inactivated vaccs
  • Enable the slow release of vaccine antigens into body to enhance immune recognition and response
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10
Q

What are the preferred outcomes of vaccination?

A
  • Generate a protective immune response
  • Long term immunity
  • Stimulation of long lives memory (MUST stimulate memory cell production)
  • Rapid secondary response
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11
Q

Is CMI more effective against cytopahtic or non cytopathic viruses?

A

-Non Cytopathic

better against viruses than have no extracellular phase

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12
Q

List the different types of vaccines available

A
  • Live
  • Marker
  • Inactivated
  • Subunit (selected proteins/ peptides of pathogen)
  • Mulivalent (multiple pathogens in one administration)
  • Recombinant proteins
  • Naked DNA
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13
Q

What are the pros/ cons of live vaccine?

A
  • Get both CMI and Ab responses
  • DIVA potential (can distinguish between actual pathogen)
  • Potential to revert to virulence
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14
Q

How do live vaccines work?

A
  • Infect host cell to limited degree

- Results in CTL recognition of virus and memory cell formation

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15
Q

Give examples of live vectored vaccines (recombinant organisms)

A

-Pox viruses (e.g. adenovirus)

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16
Q

Describe inactivated vaccines

A
  • Killed whole OR part of the oragnism
  • Unable to repicate so NO clinical disease
  • Retain degree of antigenicity
  • Benefit: no danger of virulence
  • Cons: only structural proteins present, adjuvant needed
  • Good at stimulating Ab but not CTL
  • Exogenous antigen processing and presentation by class 2 pathway; Th2 responses &cytokines enhance differentiation of B cells into plasma cells, memory cells established
17
Q

Give an example for inactivated vaccine examples

A
  • FELV gp70

- Equine flu

18
Q

What is hypoimmunisation?

A

Allergen testing via IgE ELISA skin test

  • Allergen identified, hypoimmunisation to alter bias of immune response and get a reduction in clinical signs
    (i. e. change bias means switch it to different isotype)