Immunisation Flashcards

1
Q

Define immunisation

A

The process where a susceptible individual is rendered immune to an infection.

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2
Q

Describe the immune response following immunisation.

A
  • Vaccines take advantage of the active immune system’s ability toremember an infection through memory B cells.
  • Vaccine is injected & immune system recognises & responds to it by producing pro-inflammatory cytokines & pro-inflammatory chemokines which attract immune cells to the site of injection.
  • Dendritic cells recognise PAMPs. Dendritic cells take up & present the antigens on their surface & migrate towards the lymph nodes.
  • At lymph nodes, Dendritic cells interact w/ Cytotoxic T Cells (CD8) & Helper T Cells (CD4).
  • T Helper Cells assist w/ differentiation of naive B Cells to produce Memory B Cells
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3
Q

What is active immunity? What is passive immunity?

A

Passive - preformed antibodies from another individual, giving temporary protection.
- Mother will pass IgG antibodies across placenta & through breast milk.
- You can give immunoglobulins which are taken from donors* (people who have already had the disease or vaccine).

Active - involves the person’s immune system - longer lasting & involves memory.

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4
Q

Types of active vaccines?

A

Live attenuated vaccines

Inactivated whole cell vaccines

mRNA

Viral vector

Inactivated toxin

Subunit recombinant proteins

Subunit chemically purified

Polysaccharides

Conjugated polysaccharides

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5
Q

What are live attenuated vaccines? Examples? Pros & cons? Who is it not suitable for?

A

Pathogen is capable of replicating but is in weakened state.
- Attenuated by serial passage through tissue culture or an animal model - becomes more adapted to these environments & less adapted to cause illness in humans.

Examples:
- Rotavirus vaccine
- MMR vaccine
- Influenza vaccine
- Shingles vaccine
- Chickenpox vaccine (varicella zoster)
- BCG vaccine against TB
- Yellow fever vaccine
- Oral typhoid vaccine (not the injected vaccine)
- Oral polio vaccine

Pros:
- Pathogen replicates in recipient = strong & memorable immune response = fewer doses.
- More closely resembles natural infection.

Cons:
- Potential for reversion - a mutated version can become the full version
- Potential for sustained vaccine strain infection
- Vaccine that is live can be spread in faeces

Not suitable for:
1. Immunocompromised patients
2. Pregnant women - risk of live vaccine crossing the placenta & infecting the baby!!

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6
Q

What are Inactivated whole cell vaccines? Examples? Pros vs Cons?

A

Grow pathogen then kill it by chemical or physical processes

Examples:
- Hepatitis A
- Polio
- Rabies
- Inactivated polio (Salk)

Pros:
- Cannot cause disease because pathogen is dead.
- Can be given to immunocompromised patients.

Con:
-Doesn’t usually provide protection that is as strong as live vaccines, so several booster jabs could be required.

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7
Q

How do mRNA vaccines work? Examples?

A

mRNA from vaccine is translated into antigen proteins when inside the cell.
- stimulates an immune response.

Examples
- Pfizer BioNTech COVID-19
- ModernaCOVID-19

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8
Q

What are viral vector vaccines? Examples?

A

Modified version of a different virus is used to trigger an immune response.
- works by attaching target antigens onto a host which is unable to cause disease in humans.

Example
-AstraZenecaCOVID-19

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9
Q

What is an inactivated toxin vaccine? Examples?

A

Toxins from bacteria are chemically treated to eliminate toxicity whilst maintaining immunogenicity.

Examples
- Diphtheria
- Pertussis

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10
Q

What are subunit recombinant proteins? Examples? Pros vs cons?

A

Specific viral protein (antigen) is produced in either yeast or insect cell systems.

Examples
- Hepatitis B
- Human Papillomavirus (HPV)
- Meningitis B

Pros:
- only injecting the antigen so vaccine can’t cause disease.

Cons:
- don’t have such long lasting immunity as live vaccines.
- Require adjuvants which strengthen & lengthen immune response, increasing chance of sore arm.

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11
Q

What are Subunit chemically purified vaccines? Examples?

A

components of a pathogen are purified for use in a vaccine

Example
- Influenza

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12
Q

What are polysaccharide vaccines? Examples? Pros vs cons?

A

Purified bacterial polysaccharide.

Examples
- Some meningococcal vaccines
- Some pneumococcal vaccines
- Salmonella

cons
- Produce poor immune response in young children.
- B cell receptors link when attaching to polysaccharide & produce a plasma cell that makes antibodies-doesn’t involve any T-cells so response is smaller

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13
Q

What are conjugated polysaccharide vaccines? Examples? Pro?

A

Purified bacterial polysaccharide linked to a protein conjuagte.
- Usually diptheria or tetnus toxin.

Examples
- Haemophilus Influenzae type b (Hib)
- Pneumococcal
- Meningococcal e.g. MenC & MenACYW

Pros
- T-cell dependent response = gives memory response = last longer & works for children.

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14
Q

What are adjuvants?

A

Agents that stimulate the immune system

e.g. Aluminium phosphate & hydroxide

Thought to sequester antigen & cause inflammation = attracting immune cells.

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15
Q

How are vaccines most commonly used? Who gets which vaccines?

A

Prophylaxis - pre-exposure

Children - according to the UK vaccine schedule.

Adults:
- 65 yrs - flu vaccine every year
- 65 yrs - pneumococcal
- 70 yrs - varicella zoster (shingles vaccine)

Pregnant women - flu vaccine & pertussis (whooping cough) from 16 week gestation - mainly given to provide passive immunity to baby- were getting whooping cough when they were too young to be vaccinated.

Adults & children at high risk due to underlying health conditions.

Those at risk due to occupation, lifestyle or contacts

Travellers

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16
Q

Use of vaccine post exposure

A

Immunoglobulins & some vaccines can be given after an exposure to reduce the chance of an individual developing disease or reducing the severity.

Examples of when:
- Wounds at high risk of tetanus = specific immunoglobulin
- Potential rabies exposure = course of vaccine +/- specific immunoglobulin.
- Unvaccinated contact w/ confirmed measles case = vaccine (or if contraindicated - consider normal immunoglobulin).

17
Q

What are adverse effects related to vaccines?

A

Most common- local reactions: pain, swelling, redness

General systemic effects: fever, headache, malaise

Rash - e.g. MMR, VZV

Anaphylaxis is rare

Other rare adverse events specific to a vaccine:
- Yellow Fever - encephalitis (inflammation of the brain).
- BCG - osteitis(inflammation of bone)
- Rotavirus - potential increased risk of intussusception(telescoping of the intestine causing a blockage).

18
Q

Contraindications- people who cannot receive vaccines?

A

Consider:
- History of anaphylaxis
- Immunosuppression
- Pregnancy

Immunisations may need to be deferred when:
- Acutely unwell
- Other vaccines given recently
- immunoglobulin therapy

19
Q

What can cause vaccine failure?

A

Primary vaccine failure: fails to mount an immune response
- Vaccine factors e.g. administration error, manufacturing error, incomplete strain coverage.
- Host factors e.g. immunodeficiency
- Inappropriate vaccine schedule

Secondary vaccine failure: immunity develops initially but then wanes.

20
Q

The UK vaccine schedule?

A

Vaccines begin at 8 weeks!

8 weeks:
- pertussis (whooping cough)
- polio
- influenza B
- Hep B
- Rotavirus

12 weeks:
- same
- first dose of MMR - given IM

16 weeks:
- same + MenB

4-6 years:
- second dose of MMR