Lecture 6: Vaccines and Vaccinations Flashcards

1
Q

How do vaccines work? general

A

Vaccines work by mimicking disease agents and stimulating the immune system to build up defenses against them.

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2
Q

What is the balance for vaccines

A

Vaccine efficacy and vaccine assosicated risk

Ability of a vaccine to work as intended to protect from illness to the probability of increased adverse event that harm the indiviuals or population

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3
Q

Weighing the risks and benefits of a vaccine

: Areas of consideration

A

he incidence, severity, morbidity and mortality resulting from adverse vaccine reactions,

Case investigation to determine whether the vaccine presents a new suspected risk,

The probable mechanism and underlying cause of any vaccine reactions,

The preventability, predictability and reversibility of the risk of a vaccine reaction occurring,

The risks associated with alternative vaccines that protect against the same disease,

The risks associated with not vaccinating, i.e. the risks arising from the infectious disease in unvaccinated individuals.

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4
Q

Types of vaccines and example

A
  1. Live attenuated
    TB
    Measles
    Yellow Fever
    Rotvirus
  2. Inactivated (killed antigen)
    Whole cell whooping cough
    Inactivated polio virus
  3. Subunit
    Acellular whooping cough
    Hep B

4.Toxiod
Tetanus

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5
Q

Live Attenuated Vaccines (LAV):
Definiation
Immune response

A

LAVs are derived from disease-causing pathogens (viruses or bacteria) that have been weakened under laboratory conditions. They will grow in a vaccinated individual, but because they are weak, they will cause no disease or very mild disease.

Immune response
LAVs stimulate an excellent immune response, that is nearly as good as compared to an infection with the wild-type pathogen.

Live microorganisms provide continual antigenic stimulation giving sufficient time for memory cell production.

In the case of viruses or intracellular microorganisms where cell-mediated immunity is usually desired, attenuated pathogens are capable of replicating within host cells

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6
Q

Live Attenuated Vaccines (LAV):
Safety and Stability

A

Attenuated pathogens have the very rare potential to revert to a pathogenic form and cause disease in vaccinees or their contacts.

Immuno compromised are vunerbale as they can not clear the attenuated pathogen and therefore have the risk of causing the disease that is trying to be vaccinated against eg HIV

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7
Q

LAV:
Immune response vs safety and stability

A

Immune response:
Live micorbes provide continual antigenic stimulation, giving sufficent time for memory cell production

Attenuated pathogens are capable of replicating within the host
EXCELLENT immune response

Safety and Stability
Attenutated Pathogens can revert to orginal form and cause disease
potential harm to people with compromised immune system

Sustained infection

Contamination of tissue culture
immunisation cultures
not given in preg

less safe compared to inactivated

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8
Q

Inactivated (killed antigen) vaccines:
Def
Immune response

A

Definition
Inactivated vaccines are made from microorganisms (viruses, bacteria, other) that have been killed through physical or chemical processes. These killed organisms cannot cause disease.

Immune response
Inactivated whole-cell vaccines may not always induce an immune response and the response may not be long lived.

Several doses of inactivated whole-cell vaccines may be required to prime a sufficient immune response.

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9
Q

Inactivated (killed antigen) vaccines:
Safety and Stability

A

Safety and stability

Inactivated whole-cell vaccines have no risk of inducing the disease they are given against as they do not contain live components.

They are considered more stable than LAV vaccines.

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10
Q

Inactivated (killed antigen) vaccines:
Immune response vs safety and stability

A

IR:
May not give immune response in first dose
Repsonse may not be long lived (many doses)
LESS STRONG immune response than LAV

Safety:
No risk of inducing disease (no live components)
Safer than LAV

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11
Q

Subunit vaccines:
Def
Immune response

A

Definition
Subunit vaccines, do not contain live components of the pathogen. They differ from inactivated whole-cell vaccines, by containing only the antigenic parts of the pathogen. These parts are necessary to elicit a protective immune response.

Immune response
This precision comes at a cost, as antigenic properties of the various potential subunits of a pathogen must be examined in detail to determine which particular combinations will produce an effective immune response within the correct pathway.

Often a response can be elicited, but there is no guarantee that immunological memory will be formed in the correct manner.

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12
Q

Subunit Safety and stability

A

Like inactivated vaccines, subunit vaccines do not contain live components and are considered as very safe.

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13
Q

Subunit
Immune response vs safety

A

IR:
Must determine which combination of antigenic properties will make an effective immune response with the correct pathway

A response may be elicted but with no guarantee that memory will form for future repsonses

LESS STRONG THAN LAV

Safety:
Have no live components - no risk of infection
Safer than LAV

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14
Q

Toxiod vaccine Defination

A

Definition
Toxoid vaccines are based on the toxin produced by certain bacteria (e.g. tetanus or diphtheria). The toxin invades the bloodstream and is largely responsible for the symptoms of the disease.

The protein-based toxin is rendered harmless and used as the antigen in the vaccine to elicit immunity.

To increase the immune response, the toxoid is adsorbed to aluminium or calcium salts, which serve as adjuvants.

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15
Q

Toxoid vaccine safety and stability

A

Safety and stability

Toxoid vaccines are safe because they cannot cause the disease they prevent and there is no possibility of reversion to virulence.

The vaccine antigens are not actively multiplying and do not spread to unimmunised individuals.

They are stable, as they are less susceptible to changes in temperature, humidity and light.

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16
Q

Toxoid vaccine
immune response vs safety

A

IR:
Several doses and needs adjuvant
not highly immunogenic

Safety:
Cant cause disease it prevents
rare local and systemic effects
stable and long lasting

17
Q

RNA vaccine

A

RNA coding for protein antigens of the pathogen (for example spike protein antigens of SARS-CoV-2 causing Covid 19) is injected into the person having the vaccine
This RNA is translated into the pathogen proteins
There is no risk of catching Covid 19 because its not the whole, viable organism
Your body recognises the proteins as foreign and makes antibodies

18
Q

Combination vaccines: Def and benefit

A

Combination vaccines consist of two or more antigens from different pathogens in the same preparation, eg MMR

Combination products simplify vaccine administration and allow for the introduction of new vaccines without requiring additional health clinic visit and injections.

19
Q

Combination vaccine 3 benefits

A

1 - Reducing the cost of stocking and administering separate vaccines,

2 - Reducing the cost of extra health care visits,

3 - Facilitating the addition of new vaccines into immunization programmes.

20
Q

Components of vaccines

A

Vaccines include a variety of ingredients including active component (whole pathogen, antigens,toxoid or mRNA) stabilizers, adjuvants, antibiotics, and preservatives.

21
Q

Stabilisers:
purpose
effect if not present
factors on stability
example

A

Stabilisers are used to help the vaccine maintain its effectiveness during storage.

Instability can cause loss of antigenicity and decreased infectivity of LAV.

Factors affecting stability are temperature and acidity or alkalinity of the vaccine (pH).

Stabilizing agents include MgCl2

22
Q

Adjuvants:
purpose
Example

A

Adjuvants have been used for decades to improve the immune response to vaccine antigens, most often in inactivated (killed) vaccines.

In conventional vaccines, adding adjuvants into vaccine formulations is aimed at enhancing, accelerating and prolonging the specific immune response to vaccine antigens.

EXAMPLE: Aluminium salts
They slow the escape of the antigen from the site of injection, thereby lengthening the duration of contact between the antigen and the immune system (i.e. macrophages and other antigen-receptive cells).

23
Q

Antibiotics
purpose

A

Antibiotics (in trace amounts) are used during the manufacturing phase to prevent bacterial contamination of the tissue culture cells in which the viruses are grown.

24
Q

Preservatives
Purpose
Example

A

Preservatives are added to vaccines to prevent bacterial and fungal growth.

They include a variety of substances, for example Thiomersal, Formaldehyde, or Phenol derivatives.