Vaccinology Flashcards

1
Q

True or False. Vaccines are usually used as a key metric in level of development.

A

True

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2
Q

True or False. Vaccines are the most cost-effective method for dealing with infectious threats to human populations,

A

True

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3
Q

How is immunological memory/ vaccine response measured?

A

IgG titre

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4
Q

What is immune memory?

A

It is the increased ability to proliferate of memory T/B cells post infection

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5
Q

What is R in vaccinology?

A

Rate of Ab decay/Rate of Ab synthesis

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6
Q

How does the Abs produced after vaccination change upon multiple doses?

A

1st dose: primarily IgM, some IgG later on
Subsequent doses: Early IgG response&raquo_space;» IgM prod.

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7
Q

Responses to vaccines in a population are _____.

A

Heterogenous

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8
Q

What is herd immunity?

A

It is when individuals who are not immune to a pathogen are protected from exposure by the large amounts of immune individuals within the community

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9
Q

When does pathogen spread stop?
(In relation to infection and critical threshold)

A

When P(infection)<critical threshold

threshold is pathogen & population specific

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10
Q

Higher pathogenicity is associated with ____ critical threshold?

A

Higher

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11
Q

What type of vaccines typically completely block infections?

A

Live attenuated

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12
Q

Does a vaccine protect a person from infection or from severe disease?

A

Mostly protection from severe disease

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13
Q

How do vaccines protect a person from severe disease?

A

1) Vaccines are usually delivered IV/IM (cos its easier) but many pathogens infect mucosal sites
- localised dmg limited by systemic immunity

2) Systemic vax → ↓no. pathogens in bodily secretions → ↓ transmisibilty

3) Hybrid immunity
- vax + recovery from mild infection
→ ↑ immunity + longer term

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14
Q

What are 3 variables that complicate public vaccination policy?

A

1) Poverty/ social structure/ politics/ infrastructure
2) costs
3) public complacency and mistrust

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15
Q

What are some requirements for an effective vaccine?

A

1) Safety
2) Induce protective immunity
3) Long-lasting protection
4) Low cost
5) Genetic stability
6) Storage stability
7) Delivery (Oral/needle)

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16
Q

What are the 5 types of vaccines in order of decreasing safety but increasing efficacy?

A

1) Live attenuated (mimic natural infection)
2) Killed/dead viral pathogens
3) Pseudoviruses/virus-likes proteins
4) Viral-proteins and peptides sub-unit vaccines
5) DNA/RNA vaccines

17
Q

What is the relationship between vaccine safety and efficacy?

A

Inverse/negative relationship

18
Q

What are 2 examples of vaccine cocktails?

A

1) MMR/MMR-V
2) 6-in-1 (Diptheria, Tetanus toxoid, acellular Pertussis, Haemophilus influenzae B, Polio, Hep B)

19
Q

What are some limitations of live attenuated vaccines?

A

1) need to ensure 0 contamination
2) hazardous production
3) possible reversion to virulence*
4) req. proper refrigeration
5) not safe for immuno-compromised

20
Q

What are some limitations of killed pathogens vaccines?

A

1) need to ensure successful killing
2) adverse effects (eg. TAB → fever malaise, whole cell pertussis → febrile convulsions)

21
Q

What are some limitations of purified component vaccines?

A

1) tedious prod. and purification
2) expensive
3) low yield
4) need adjuvant/carrier

22
Q

What are some routes of vaccine administration?

A

1) Hypodermis
2) Transcutaneous
3) Oral
4) Nasal

23
Q

What are the differences between Mucosal and Systemic vaccination?

A

Mucosal:
- CD4+ > CD8+
- Nasal/oral administration
- prevents both initial stages and blocks development
- BOTH IgA and IgG
- induces local and systemic immune response
- immunity @ distant mucosal sites (via homing receptors

Systemic:
- CD8+ > CD4+
- Needle (cross-contamination + training)
- block disease development only AFT pathogen cross mucosal barrier and establish infection
- only IgG
- only systemic immunity

24
Q

Why aren’t all vaccines for respiratory infection made for mucosal administration?

A

It’s not always possible based on form and f(x) of the vaccine construct.

25
Q

What is an adjuvant?

A

An agent w/o any specific antigenic effect but may be immunogenic to ↑ response to vaccines

26
Q

Which form of vaccines require adjuvants?

A

Purified proteins and sub-units vaccines

27
Q

Why do purified proteins, sub-units, vaccines require adjuvants?

A

because they are poorly immunogenic and readily degraded by proteolytic system

28
Q

What are the some possible functions of adjuvants?

A

1) ↑Immunogenicity
2) Prolong exposure to the immune system
3) Ag sparing (↓ Ag/dose)
4) Dose sparring (↓doses needed)
5) Stimulate innate immunity → augment adaptive response

29
Q

What are the 2 types of vaccine adjuvants?

A

1) Mineral salts (Aluminium salts but can cause Al intoxication)
2) Emulsions (allows slow Ag release but ↑toxicity)