L28 - Intro To Vaccination Flashcards

1
Q

How was vaccination first discovered

A

Having cowpox decreased chances of acquiring smallpox

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2
Q

What is considered passive immunity? What are the 2 types

A

The transfer of antibodies from an immune to non-immune individual

Natural - mother to child via placenta or colostrum

Artificial - transfer of antibodies derived from blood of immune people

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3
Q

How is therapeutic anti-sera produced

A
  • using donor animal
  • it is immunised with non-lethal doses of an antigen
  • induced immune response produced neutralising antibodies
  • blood from donor animal is collected and antibodies r purified from the blood
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4
Q

What are the current applications of antibody transfers

A
  1. Rapid treatment during acute illness of patients
  2. Preventative measure
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5
Q

Pros and cons of antibody transfers

A

Pros
- quick acting
- support a deficient immune system
- beneficial to high risk individuals

Cons
- protection fades overtime
- intravenous injection
- serum sickness
- expensive
- complicated to manufacture

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6
Q

How are monoclonal antibodies produced

A
  1. Mouse challenged with antigen
  2. WBC (B cells) taken from spleen and fused with myeloma cells
  3. The replicate to produce Abs indefinitely
  4. Harvest monoclonal antibodies
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7
Q

Pros of monoclonal antibodies

A
  • single specificity
  • unlimited supply
  • even Abs w rare specificity can be isolated
  • Abs can be manipulated
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8
Q

How to humanise a mouse monoclonal antibody, why is it needed?

A

Immune recognises mouse antibody as foreign antigen so might cause serum sickness

Replace the CDR (complementarity determining region) of a human monoclonal abs w CDR derived from mouse monoclonal antibody

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9
Q

What is the modern way of making monoclonal antibodies that are easier

A
  • directly from B cells
  • phage display
  • EBV transformation
  • in vitro expansion and selection
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10
Q

What are the 3 principles of vaccination

A
  • introduce immune system to pathogen in controlled environmen t
  • cause immune system to remember the pathogen and respond to it
  • enable effective clear of pathogen to prevent disease
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11
Q

What is the ideal vaccine

A
  • long lasting immunity
  • safe
  • stable in field conditions
  • easy to store and administer
  • Single dose
  • pathogen evolution proof
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12
Q

What is live attenuated vaccine

A

Pathogenic strains in which the virulent genes are deleted or modified

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13
Q

Why is live attenuated vaccine more effective than killed whole organism

A

More effective immune recognises folded proteins. Killed proteins are unfolded

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14
Q

What is the significance of eggs in traditional vaccine technology

A

When virus injected into eggs diff parts of the egg lets diff virus replicate

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15
Q

Limitations to traditional vaccine

A
  • not all grown in culture
  • live (safety for lab people)
  • expense
  • insufficient attenuation
  • reversion to infectious state
  • storage
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16
Q

What is the cons of using live attenuated and killed whole organism

A
  1. Needs to be stored cold
  2. Several doses needed
17
Q

What is toxoid

A

Vaccine using toxin derived from the pathogen

18
Q

Describe the use of subunit for vaccines? Pros n cons?

A

Subunit includes: purified protein, recombinant protein, polysaccharide, peptides)

Don’t use entire pathogen but components
Pros: no extraneous pathogenic particles
Cons: protein may differ when not in Situ, production can be expensive

20
Q

Describe vector vaccine

A

Antigen genes inserted to vaccinia virus able to elicit neutralising antibodies