Bacterial and Viral Vaccines Flashcards

1
Q

Who first tested out the smallpox vaccine?

A

Benjamin Jesty - 1774

Edward Jenner 1796 (MORE POPULAR)

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2
Q

After the smallpox vaccine, when was the next vaccine made?

A

Almost 100 years later in 1885

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3
Q

What is the goal of immunisation?

A

To allow the body to protect itself from infectious diseases

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4
Q

What are the two types of immunity?

A

Innate

Acquired

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5
Q

What are the two types of acquired immunity?

A

Active - Made in own body

Passive - Ready made antibodies

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6
Q

What are the subcategories of active immunity?

A

Natural (disease exposure)

Artificial (Immunisation)

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7
Q

What are the subtypes of passive immunisation?

A

Natural - maternal antibodies

Artificial - exogenous antibodies

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8
Q

At what R0 (the no. of people 1 sick person can affect) is transmission halted?

A

If effective R0 is reduced < 1 then transmission is halted

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9
Q

What is herd immunity?

A

Form of immunity that occurs when vaccination of a significant proportion of a population provides a measure of protection for individuals that are not immune.

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10
Q

What is the Herd immunity threshold?

A

Percentage of fully immune individuals required to stop the spread of disease

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11
Q

How do you calculate the Herd Immunity threshold?

A

HIT = 1 -1/R0

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12
Q

What are the cells in the innate immune system?

A
Macrophage
Dendritic cell
Mast cell
NK cell
Granulocytes
Complement proteins
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13
Q

Which cells are present in the adaptive immune response?

A

B cells - antibodies

T cells - CD4/CD8

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14
Q

What cells overlap between the innate and acquired response?

A

NK cells

gamma delta T cell

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15
Q

How does the body respond to a vaccine?

A

APCs present part of the antigen on the cell surface

APCs present antigen to naive T cells in the LN where they are activated

B cells activate in response to antigens - some B cells become plasma cells which produce specific antibodies and neutralise infection + Ab dependent cellular cytotoxicity

Attenuated Vx = T cell virus clearance

Memory cells produced

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16
Q

Does natural immunity occur after infection?

A

Microbial components give rise to a protective immune response

Vaccines need adjuvants to make it more potent

17
Q

What are inactivated vaccines?

A

Whole microorganism destroyed

[by heat, chemicals, radiation or antibiotics (e.g. Influenza, cholera, polio)]

18
Q

What are the advantages of inactivated vaccines?

A
  • Stable
  • Constituents clearly defined
  • Unable to cause the infection
19
Q

What are the disadvantages of inactivated vaccines?

A
  • Need several doses
  • Local reactions common
  • Adjuvant needed
  • Shorter lasting immunity
20
Q

What are attenuated vaccines?

A
  • Live organisms modified to be less virulent
  • Examples
  • Measles, mumps, rubella, yellow fever
21
Q

What are toxoid vaccines?

A

Inactivated toxic components

Examples: Tetanus, diphtheria

22
Q

What are subunit vaccines?

A
  • Protein component of the microorganisms or synthetic virus like particles.
  • Lacking viral genetic material and unable to replicate.
  • Examples: Hepatitis B, HPV
23
Q

What is a conjugate vaccine?

A
  • Poorly immunogenic antigens paired with a protein that is highly immunogenic (adjuvant)
  • Examples: Haemophilus influenzae type B
24
Q

What is a heterotypic vaccine?

A

Pathogens that infect other animals but do not cause disease or cause mild disease in humans
• Examples: BCG

25
Q

What is a viral vectored vaccine?

A

• Use a modified virus (e.g. adenovirus) to deliver
genetic code for an antigen.
• Examples: Ebola, Janssen and AZ COVID vaccines

26
Q

What is a nucleic acid vaccine?

A
  • Use DNA/RNA from the pathogen.

* Examples: Pfizer and Moderna COVID vaccines

27
Q

What is the difference between monovalent and multivalent?

A
Mono = 1 antigen
Multi = multiple antigen (e.g. pneumococcal which has 21 antigens)
28
Q

What are the components of a vaccine?

A
Active components
Adjuvants
Antibiotics
Stabilisers
Preservatives
Trace components
29
Q

Serious reactions are uncommon

A

Serious reactions are uncommon

30
Q

Why are vaccination programmes important?

A

• Vaccine should be administered before the age
related peak incidence of the disease.
• Targeted vs widespread.
• To eliminate a disease the effective R0 needs to be <1.
• ?requirement for catch up campaigns.
• Endemic vs Epidemic infections.

31
Q

What are the barriers to vaccination?

A

Access
money
Anti vax campaigns

32
Q

What are the prerequisites for successful disease eradication?

A
  • No animal reservoir
  • Antigenically stable pathogen with only one (or small number of) strains
  • No latent reservoir of infection and no integration of pathogen genetic material into host genome
  • Vaccine must induce a lasting and effective immune response
  • High coverage required for very contagious pathogens
33
Q

Do vaccines have a good impact?

A

Yes

34
Q

What are the side effects of vaccines?

A
  • Adenoviral vectored vaccines
  • VITT
  • 14.2 per million doses
  • CLS
  • Pfizer
  • Lymphadenopathy
  • Myocarditis