T1 L8: Vaccines Flashcards

1
Q

What is variola?

A

The virus that caused small pox before it was eradicated

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2
Q

What are some examples where passive immunisation is used?

A
  • Immunoglobulin replacement in antibody deficiency
  • VZV prophylaxis eg. during exposure during pregnancy
  • Anti-toxin therapies after a snake bite
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3
Q

Which type of immunisation is temporary?

A

Passive immunisation because the antibodies will be metabolised

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4
Q

What is VZV?

A

Chicken pox

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5
Q

What is the effect if chicken pox during pregnancy?

A

Can cause foetal complications

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6
Q

What is active immunisation?

A

It stimulates an adaptive immune response without any apparent infection because the pathogen is inactive

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7
Q

What are some infections that the body can’t produce long-lasting protective immunity against?

A

TB
HIV
Malaria

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8
Q

What are the possible components of a vaccine?

A

Antigen
-Stimulates an antigen-specific T and B-cell responses

Adjuvants
-Immune potentiators to increase the immunogenicity of the vaccine

Excipients
-Various diluents and additives required for vaccine integrity

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9
Q

What does attenuated mean?

A

Weakened

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10
Q

What are some examples of live-attenuated vaccines?

A
Measles
Mumps
Rubella
Polio (Sabin)
BCG
Cholera
Zoster
VZV
Live influenza
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11
Q

How can organisms be attenuated?

A

-Prolonged culture ex vivo in non-physiological conditions

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12
Q

What are the positives of a live vaccine?

A
  • They replicate within the host to create highly effective and durable responses
  • Good CD8 response
  • Repeated booting not required
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13
Q

What are some negatives of using live vaccines?

A
  • Hard to store because they have a short half-life
  • May revert to wild type Eg. vaccine associated poliomyelitis
  • Immunocompromised people may develop clinical disease
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14
Q

What is Poliomyelitis?

A

An enterovirus that establishes infections in the oropharynx and Gi tract but then spreads via lymphatics and then through the blood

1% of patients develop neurological symptoms leading to denervation and flaccid paralysis because the virus replicated in the NS

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15
Q

What is the Sabin oral polio vaccine (OPV)?

A
  • A live-attenuated vaccine
  • Highly effective
  • 1 in 750,000 develop vaccine associated paralytic polio

Viable virus can be recovered from stool after immunisation so it establishes some protection in non-immunised people

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16
Q

What is the Salk injected polio vaccine (IPV)?

A

An inactivated vaccine

Better suited for endemic area where benefits of higher efficacy outweigh risks of vaccine-associated paralysis

UK switched to IPV in 2004

17
Q

What is a Ghon focus?

A

The calcified TB lesion visible in a chest X-ray

18
Q

What does BCG stand for?

A

Bacille Calmett-Guerin

19
Q

How does the BCG vaccine work?

A

It increases IFN-gamma cell responses to mycobacterium bovis therefore creating protection against mycobacterium tuberculosis

It 80% prevents dissemination but has little to no effect on pulmonary TB

20
Q

How are pathogens in vaccines inactivated?

A

The entire organism is used but physical or chemical methods are used to destroyed viability
Eg. Formaldehyde

21
Q

What effect does an inactivated vaccine have on B-cells and T-cells?

A

The inactivated organism stimulates B-cells and is taken up by antigen-presenting cells to stimulate antigen-specific CD4 T-cells

Minimal CD-8 response

Responses are less robust compared to live-attenuated vaccines

22
Q

What are some advantages of killed vaccines?

A
  • No potential for reversion
  • Safe for the immunocompromised
  • Stable in storage
23
Q

What is pathogen reversion?

A

When it turns back to it’s original active virulent form

24
Q

What are some disadvantages of killed vaccines?

A
  • Response is weaker compared to live vaccines

- No CD8 response so responses are less durable and boosters are needed

25
Q

What is antigenic drift?

A

Slow accumulation of mutations

26
Q

What is antigenic shift?

A

When major antigens combine Eg. Spanish flu

27
Q

What are toxoids?

A

Toxins that have been chemically detoxified to toxoids

28
Q

What is the function of polysaccharide capsules?

A

They make the pathogen immune to phagocytosis

29
Q

What are subunit vaccines with polysaccharide capsules?

A

Vaccines for organisms formed of purified polysaccharide capsules which aim to improve opsonisation

30
Q

What is vaccine conjugation?

A

Combines a strong antigen with a weak one to boost response

Eg. protein carrier attached to polysaccharide antigen

31
Q

What are some positives of subunit vaccines?

A
  • Extremely safe
  • Works well where primary infection can be prevented by an antibody response
  • Works well where virus cannot be easily cultured Eg. HPV and Hep B
32
Q

What are some negatives of subunit vaccines?

A
  • Development requires detailed knowledge of virology, pathogenesis, and immunology
  • Specialised and expensive production
  • Weaker immune responses so boosting is often needed
33
Q

What are some novel adjuncts?

A

Toll-like receptor ligands (CPG repeats)

34
Q

How do mRNA vaccines work?

A

A genetic sequence is delivered and then the host cells produce encoded antigens which stimulates an immune response

35
Q

How is a viral vector used in vaccines?

A

Viral vector vaccines use a modified version of a virus that is different from the virus being targeted to deliver important instructions to our cells