13. Lecture Flashcards

1
Q

• Active immunization

A

viral vaccines
• preventive method
• most widespread form to control viral diseases and prevent economic losses
• drawback: coexistence with the virus
→ Most vaccines do not prevent infection!

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2
Q

general rules in viral vaccines/immunization against viral disease

A
  • inhibitory effect of maternal antibodies
  • negative phase
  • vaccination schedules
  • avoid immunosuppression
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3
Q

vaccine types

A
  • monovalent

* polyvalent

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4
Q

live virus vaccines; Virulent virus vaccines

A

(wild type)

•different entry site

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5
Q

natural attenuated vaccines

A

•Naturally occurring mutants (isolation)

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6
Q

Artificially attenuated viruses

A

• serial passages (in alien host, in embryonated eggs, in
cell cultures)
• selection of thermo-sensitive mutants
• genetic modification (deletion mutants)
→ marker, DIVA vaccines (IBR, Aujeszky’s disease)

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7
Q

Heterotypic vaccines

A

are pathogens of other animals that either do not cause disease or cause mild disease in the organism being treated
• Marek’s disease – Turkey herpes
• smallpox – vaccinia virus

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8
Q

Virus-vectored vaccines

A

• introduction antigens into apathogen viruses

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9
Q

Inactivated (killed) vaccines:

A

→ The virus is not able to multiply

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10
Q

adjuvants (enhancing)

A

•slow antigen release, depo-effect
•immunostimulation
•AlOH3
, saponine, oil

boostering is necessary in inactivated vaccines

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11
Q

Route of administration in live and inactivated vaccines

A

live: natural/injection
inactivated: injection

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12
Q

Virus dose (~cost) in live and inactivated vaccines

A

live: low
inactivated: high

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13
Q

Number of doses in live and inactivated vaccines

A

live: single
inactivated: multiple

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14
Q

need of adjuvant in live and inactivated vaccines

A

live: no
inactivated: yes

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15
Q

Duration of immunity: live and inactivated vaccines

A

live: longer
inactivated: shorter

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16
Q

Antibody response: live and inactivated vaccines

A

live: IgG, IgA
inactivated: IgG

17
Q

Cell-mediated response: live and inactivated vaccines

A

live: good
inactivated: poor

18
Q

Heat instability in tropics in live and inactivated vaccines

A

live: yes
inactivated: no

19
Q

Interference: live and inactivated vaccines

A

live: occational
inactivated: no

20
Q

Side effects: live and inactivated vaccines

A

live: occational
inactivated: no

21
Q

Reversion to virulence in live and inactivated vaccines

A

live: possible
inactivated: no

22
Q

Contamination in live and inactivated vaccines

A

live: possible
inactivated: no

23
Q

subunit vaccines

A

•contains only proteins responsible for neutralization

24
Q

production of subunit vaccines

A

•purification after traditional virus production
→chromatography, iscom
• purification of proteins produced by genetically
manipulated bacteria or cells
• synthesis
→ maturation of the polypeptide!

25
Q

advantages of subunit vaccines

A
  • safe (without nucleic acid)
  • opportunity for differentiation (ELISA)
  • in experiments good efficacy
26
Q

Disadvantages of subunit vaccines

A
  • expensive
  • only parenteral administration
  • in vivo usually weaker immune response
27
Q

Anti-idiotype vaccines

A

•epitope and paratope groups
(„key and lock” theory) (receptor parts)
–> receptor only, not the actual virus
•absolutely safe vaccines

28
Q

production of Anti-idiotype vaccines

A

• animal species „A” immunized with viral antigen
→ anti-viral IgG „A” is purified
• animal species „B” is immunized with anti-viral
IgG „A”
→ anti-(IgG „A”) IgG „B” is purified
→Fab of IgG „B” ~ viral antigen
• usually with monoclonal antibodies