Vaccines Flashcards

1
Q

Variolation

A

[deliberate infection with smallpox]

Dried smallpox scabs were blown into the nose of individual who contracted mild form of disease

Upon recovery, they were immune to smallpox

Between 1-2% of those variolated died as compared to 30% when they contracted the disease naturally

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2
Q

NO mass vaccination

A

each host in contact with infected host becomes infected (with a certain probability)

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3
Q

WITH mass vaccination

A

outbreak attenuated/averted by lack of susceptible hosts

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4
Q

heard immunity threshold

A

when the proportion of immune individuals in a population reaches threshold, the spread of disease to non-immune population can be interrupted

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5
Q

concept of vaccinology

A

When exposed to a pathogen for the first time, we have no specific IgG antibodies against the pathogen -> infection can progress to disease

Over time, we produce antigen specific IgG antibodies i.e. memory immune response

Next time we’re exposed to this pathogen, we will be protected from the disease

If we were exposed to a pathogen that didn’t progress to a disease, then our bodies response would simply the generation of immune memory

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6
Q

Basic concepts of vaccines

A

Deliver to body some part/all of disease organism that imitates the pathogen but isn’t pathogenic

Both bacteria and viruses contain antigenic components that can be suitable for generating vaccines

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7
Q

types of vaccines

A
  1. Live-attenuated vaccines - e.g. measles, mumps, rubella
  2. Inactivated - e.g. hepatitis A, influenza
  3. Recombinant sub-unit - e.g. hepatitis B
  4. Toxoid - e.g. tetanus
  5. Conjugate polysaccharide-protein - e.g. meningococcal

^ a single disease may have vaccines from several types

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8
Q

Live-attenuated vaccines

A

Derived from disease-causing virus/bacteria

small dose given (enough to stimulate immune response)

immune response = identical to natural infection

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9
Q

Live-attenuated vaccines - advantages/disadvantages

A

Cheap
Adjuvants not necessary

Potential to cause pathology
Stability

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10
Q

Inactivated vaccines

A

Not alive and can’t replicate - can’t cause disease or infection even in an immunodeficient person

Dose administered by injection

First dose “primes” immune system; 2nd/3rd dose = protective immune response

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11
Q

Inactivated vaccines - advantages/disadvantages

A

Generally safer
Easy to manufacture
Improved stability

Can be costly
Hypersensitivity

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12
Q

Recombinant sub-unit vaccines

A

Comprised of one antigenic part of pathogen

Unique type of inactivated subunit vaccine that is composed of long chains of molecules that make up surface capsule of certain bacteria

Immune response to a pure polysaccharide vaccine = T-cell dependent
- Able to stimulate B cells without assistance of T-helper cells

DNA vaccines = type of recombinant vaccine

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13
Q

Toxoids vaccines

A

Toxins = major virulence factors for some bacteria which cause disease

Toxoids = forms of chemically altered toxin that are no longer pathogenic

Antibodies produced in the body neutralise toxic moiety produced during infection rather act upon organism itself

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14
Q

Toxoids vaccines - advantages

A

Highly efficacious

Safe

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15
Q

Conjugate polysaccharide vaccines

A

Prepared from extracted cellular fractions

As carbohydrates don’t illicit T-cell response, the polysaccharides are often chemically attached to a carrier protein (often toxoids)

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16
Q

Monovalent vaccine

A

designed to immunise against a single antigen/pathogen

17
Q

multivalent vaccine

A

designed to immunise against 2 or more strains of the same microorganism or against 2 or more microorganisms

18
Q

vaccine production - live attenuated vaccines

A

Pathogen passaged many times under stress conditions

Stress conditions pressure the virus to replicate differently
- Slower replication
- Loss of virulence factors

Causes virus to be attenuated -> no longer disease causing

Virus then purified and formulated

19
Q

vaccine production - inactivated vaccines

A

Whole pathogen grown and killed - heat/chemical modification (formaldehyde)

20
Q

vaccine production - Recombinant sub-unit vaccines

A

Identify sub-unit being targeted

Insert pathogenic gene into host-organism for production

Express protective antigen in safe easy-to-grow organism

Purify antigenic sub-unit and formulate

21
Q

vaccine production - Toxoid vaccines

A

Toxins are isolated from pathogen and purified

Toxins converted to toxoids (inactivated toxin) by chemical treatment

Toxoid then formulated

22
Q

vaccine production - conjugate polysaccharide vaccines

A

[Phase I]

  • Surface polysaccharide from pathogen is grown (fermentation) and isolated
  • Carrier protein is grown up separately and purified

[Phase II]

  • Any toxins on polysaccharide are chemically removed
  • Carrier protein and polysaccharide are then covalently attached together (chemical crosslinking)
  • “conjugate” then purified and formulated
23
Q

Formulation of vaccines

A

[Crucial for efficacy and stability]

  1. Active components
  2. Adjuvants
  3. Antibiotics
  4. Stabilisers
  5. Preservatives
  6. Trace components
24
Q

why do we need adjuvants?

A
  1. Stronger and longer - enhance immune response
    • Promotes rapid, long-lasting and broad immunity
    • Improves immune memory
  2. Antigen-sparing - to induce protective antibody responses with less antigen
  3. Cross-reactive immunity - induce a “broader” immune response, directed against strains/subtypes not included in vaccine
  4. Overcome weakened immunity - in elderly and immunocompromised individuals
25
Q

how do adjuvants work?

A

Slow antigen release - maintains antibody levels

Inflammatory response - stimulates DC maturation; better utilisation of antigens; induction of CD4+ (Th1)

Immunostimulation