Vaccine Control Flashcards

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1
Q

What are the aims of vaccines?

A

To elicit an immune response that will prevent or limit disease upon encounter with the target organism/antigen.

  • Prevention of disease
  • Prevention of transmission
  • Eradication of disease
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2
Q

What are examples of successful vaccines?

A
  • Smallpox
  • Polio (salk-inactivated virus, sabin-attenuated virus)
  • Diphtheria (toxoid - inactivated toxin)
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3
Q

What is the difference between passive and active immunisation?

A

Passive or active immunisation?
• Passive immunisation
• Transfer of immune sera/cells to provide protection
• Protection is immediate but short term
• Example: Rabies immune globulin- given to individuals who have been scratched/bitten/licked by rabies-infected animals
• Maternal antibodies transferred to newborn
• Transplancental transfer of IgG (acts systemically)
• Wanes by 6-9 months
• De Novo IgG production evident between 3-6 months
IgA from sucking (probably only acts in gut)

Active immunisation-vaccines
• The introduction of foreign material into a host to stimulate an adaptive immune response
• Typically involves
• The administration of a preparation that contains one or more microbial antigens
• The administration of a vector that directs the expression of one or more microbial antigens

You need a good immune response to have an effective vaccine:
• T cells
• B cells
Innate immunity (dendritic cells)

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4
Q

What does a good vaccine typically need?

A
  • Something to stimulate the innate immune system
  • T cell epitopes
  • B cell epitopes

• Live attenuated vaccines are usually more potent than subunit or inactivated immunogens
• Pathogen replication creates strong innate immune signals
• Diverse range of antigens expressed
• Higher antigen loads
Better T cell responses

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5
Q

What is an attenuated vaccine?

A
  • Attenuation of pathogens tends to be more potent
  • In can be achieved through in vitro passage (humans- monkey - human)
  • Attenuation of pathogens can be achieved through targeted deletion of virulence genes/determinants
  • Resulting virus is viable but avirulent and so it can be used as a vaccine
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6
Q

What is a subunit vaccine?

A
  • Immunise with components of pathogens rather than the whole organism
  • Hepatitis B vaccine is an example of this
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7
Q

What are toxoid vaccines?

A
  • Immunisation with inactive forms of toxins (diphtheria/tetanus)
  • Antibodies bind to native toxin and block activity
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8
Q

What are conjugate vaccines?

A
  • Consist of an antigen coupled to a carrier (can’t stimulate a T cell response and so it needs to be coupled to a protein which is termed carrier)
    Eg. Neissera meningitis -> bacterial meningitis coupled to diphtheria toxoid
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9
Q

DNA vaccines

A

DNA vaccines in the form of plasmids can also be used

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10
Q

Features of effective vaccines

A

• Safe -> vaccine must not itself cause illness or death
• Protective -> vaccine must protect against illness resulting from exposure to live pathogen
• Gives sustained protection -> protection against illness must last for several years
• Induces neutralising antibody -> some pathogens infect cells that cannot be replaced - neutralising antibody is essential to prevent infection of such cells
• Induces protective T cells -> some pathogens, particularly intracellular, are more effectively dealt with by cell-mediated responses
Practical considerations -> low cost per does - biological stability - ease of administration - few side effects

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11
Q

What is the process of sub-cloning?

A

• Sometimes it is not possible to directly clone your gene of choice into the appropriate expression vector
• Maybe due to size limitation
• Due to additional restriction sites within your gene and those used for cloning
• Or simply just technical issues associated with cloning
• To facilitate this process we can use an intermediate or shuttle plasmid in a process termed sub-cloning
• Shuttle plasmids are generally quite small
Have a greater range of restriction sites

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12
Q

What does prokaryotic expression involve?

A
  • Delivery of DNA into bacteria

- Heat shock or electroporation (calcium and heat vs voltage gradient)

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