Immunisation Flashcards

1
Q

When may eradictaed diseases reappear?

A

When vacciination stops

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is a possible consequence of stopping vaccinations?

A

Eradicated diseases may reappear

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Describe the applications of immunisation?

A

Prevent infection

Treat infection

Prevent or treat non-infectious conditions (eg. cancer)

Modify immune responses

Modify physiological processes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the two broad types of immunisation?

A

Active

Passive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe the two types of passive immunisation?

Which is more common?

A

Antibodies (more common)

Immune cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Describe the applications of passive immunisation with Ig?

A

Treat and prevent infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Describe the sources of Ig for passive immunisation?

A

Human

Horse

Monoclonal (modified mouse)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe the two types of passive immunisation with Ig?

A

Standard (pooled): derived from plasma (leftover from blood donors)

Hyperimmune: from people that have very high titres of Abs to common infections

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Describe the features of passive immunisation with Ig?

A

Short-lived

Potentially hazardous (can get immune reactions)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

List the living immunising agents for active immunisation?

A

Unattenuated

Empirically attenuated

Rationally unattenuated

Reassortants

Antigen expressed on living vector

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Describe empirically attenuated immunising agents?

Give an example?

A

Grow agent under conditions that it doesn’t like > eventually adapts > won’t be able to grow in humans anymore

e.g. BCG vaccine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Describe rationally attenuated immunising agents?

Give an example?

A

Delete genes/components from agent

None licensed at the moment
Used to have live oral cholera vaccine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Describe how immunising agents can have antigen expressed on a living vector?

Give an example?

A

Take an exisiting living vaccine > clone genes into it for virulence factors of other bugs (e.g. clone genes for e.coli adhesins into attenuated live salmonella typhi > combined travellers diarrhoea vaccine)

No examples yet

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

List the living unattenuated vaccines?

Why don’t they cause disease?

A

Respiratory adenovirus (different route)

Rotavirus (different host - attenuated from other animals)

Vaccinia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

List the living empirically attenuated vaccines for viruses and bacteria?

A

Viruses: polio (Sabin OPV), MMR, VZV, rotavirus, yellow fever

Bacteria: BCG, typhoid (Ty21a)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

List the living rationally attenuated vaccines?

17
Q

List the reassortant vaccines?

A

Rotavirus (RotaTeq)

Influenza (Not in AUS)

18
Q

List the non-replicating immunising agents?

A

Inactivated virion, bacterium

Purified product or component

Product of cloned gene

Synthetic immunogen (experimental only)

DNA vaccine (experimental only)

19
Q

List the inactivated vaccines for viruses and bacteria?

A

Viruses: polio (Salk IPV), influenza, Hep A, Japanese encephalitis, rabies

Bacteria: cholera, typhoid, pertussis, Q fever

20
Q

List the component vaccines for viruses?

A

Hep B (use recombinant DNA)

HPV (use virus-like particles)

21
Q

List the componnt vaccines for bacteria?

A

Acellular pertussis

Toxoids: diptheria, tetanus, (cholera)

Capsular polysaccharide: unmodified (23vPPV, Vi) and modified (Hib, 10vPCV, 13vPCV, MenCCV, 4vMenCV)

22
Q

Which people receive conjugated capsular polysaccahride vaccines?

23
Q

Describe the advantages of living vaccines?

A

Broader, more natural immune response

Local immunity (sometimes)

Ease of administration (sometimes - not in remote areas - need cold chain to keep bug alive)

24
Q

Describe the disadvantages of living vaccines?

A

Disease: back mutation (empirically attenuated can become virulent again), spread (to someone that is not immunised), contamination (another agent may enter, but cannot sterilise)

Failure: dead (need cold chain), pre-existing immunity (passive - from Mum), interference (might prevent immune response if infected with another organism)

25
Describe the advantages of killed vaccines?
Stable Contamination unlikely Can't spread Safe for immune deficient
26
Describe the disadvantages of killed vaccines?
Weaker immune response Higher dose Need adjuvants - more likely to cause some side effects Expensive
27
Why are vaccinations given at specific times on vaccination schedules?
FIND ANSWER Hep B at birth - can be exposed at birth Measles - passive immunity from Mum, so wait until 1 year