INF2 - E. IMMUNITY AND VACCINATION-COVERED Flashcards

1
Q

what innate immune defences do we have

A
  • skin
  • enzymes in saliva and tears
  • phagocytes
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2
Q

what are the 2 parts of acquired immune defences

A
  • natural
  • artificial
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3
Q

passive immunisation

A
  • injection of pathogen-specific pooled human immunoglobulins
  • good for post-exposure prophylaxis or if immunocompromised and can’t make antibodies
  • doesn’t confer long-term protection (antibodies degrade and break down once used)
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4
Q

active immunisation

A
  • induces immune system to make antibodies
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5
Q

natural acquired immunity (active)

A
  • contact with the disease
  • induces immune system to make antibodies through B-cells and create memory cells
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6
Q

natural acquired immunity (passive)

A
  • placenta: mother’s milk
  • antibodies transferred from milk
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7
Q

monoclonal antibodies

A
  • molecule mimics natural antibodies to neutralise a virus/bacteria
  • protects against infection or an illness
  • works immediately
  • potential to last months or longer
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8
Q

vaccines

A
  • weakened pathogen or particle that starts an immune response to make antibodies
  • helps body prevent infection
  • immune response develops after few weeks
  • provides long-term protection (boosters?)
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9
Q

artificial acquired immunity (active)

A
  • vaccines
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10
Q

artificial acquired immunity (passive)

A
  • monoclonal antibodies
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11
Q

live attenuated vaccines

A
  • triggers long-term protection without boosters
  • strongest immune response
  • whole virus or bacterium
  • avoided in immunosuppressed
  • MMR, chickenpox vaccine
  1. viruses (in host cells)/bacteria grown in culture and passaged through rounds of culture
  2. low virulence strains selected (ie - no toxins produced)
  3. attenuated/weakened strains reproduced in says chick embryo so they don’t as easily infect us but still recognised by our immune system
  4. immune response similar to natural-active, mild symptoms (we want immunogenic vaccine, not pathogenic)
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12
Q

inactivated vaccines

A
  • whole virus or bacterium
  • fewer side effects than life-attenuated
  • less vigorous immune response
  • safer for immunocompromised
  • polio, influenza vaccine
  1. viruses/bacteria cultured and killed with heat or chemicals
  2. immune response triggered but incapable of causing disease
  3. multiple doses may be needed
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13
Q

subunit vaccines

A
  • weaker immune response than live attenuated and inactivated vaccines
  • made from a piece of a pathogen, not whole organism
  • use adjuvants as immune stimulus - help vaccine work better ie - complex bit of pathogen with a metal
  • parts of bacteria/virus which are immunogenic:
    protein-based
    polysaccharide- based
    conjugate bases
  • safe for immunocompromised, elderly, young
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14
Q

toxoid vaccines

A
  • use inactivated toxins = toxiods (from bacteria) treated with heat or chemicals
  • toxoids can’t bind to cells but trigger similar immune response as toxins
  • trains immune system to neutralise toxins produced by pathogens (ie neutralises toxic activity created)
  • doesn’t target bacteria directly or microbe
  • use adjuvants as immune stimulus
  • can prevent toxin-mediated diseases
  • booster shots recommended periodically every 10 years
  • diphtheria and tetanus
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15
Q

viral vector vaccines

A
  • gene delivery systems which use harmless viruses
  • contain gene for making certain protein
  • genetic code of antigen delivered to host cells
  • host cell makes protein
  • immune response triggered upon recognition of protein ‘this is not our protein’
  • strong immune response
  • Ebola, Astrazeneca Covid vaccine
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16
Q

nucleic acid vaccines (ie - messenger mRNA vaccines)

A
  • pathogen DNA or RNA delivered via insoluble nanoparticle capsules
  • no viral vector used
  • capsules fuses with host cell membrane and release nucleic acid
  • protein made inside cell using host machinery
  • presented one surface to activate immune response
  • adaptable technology: pick whatever gene from a microbe
  • Pfizer for Covid
17
Q

vaccine boosters

A
  • pathogens evolve and mutate so new vaccine may be required ie - flu vaccine
  • booster as protection deteriorates overtime