Immunisation Flashcards

1
Q

What are the two types of immunisation?

A

Active and passive

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2
Q

What does immunisation involve?

A

using vaccines or antibody-containing preparations to provide immune
protection to provide immune protection against specific diseases

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3
Q

Describe passive immunisation

A

immediately active, effective for post-exposure prophylaxis, no memory, no need for
fully-functional immune system (eg. use in immunocompromised hosts, young, elderly)

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4
Q

Describe active immunisation

A

Vaccines - long-duration, lag before it is active, usually requires multiple immunisations

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5
Q

Describe passive immunisation

A

Passive immunisation is via immunoglobulins – provides immediate protection
 Standard immunoglobulins (human, animals) – non-specific, pooled plasma from donors,
immunoglobulins vs. many common infections
 Human hyperimmune serum (high titre) – specific, from donor with high titres of antibodies to a
specific virus, against specific (single) pathogen or antigen

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6
Q

Examples of when passive immunisation is used

A

rabies

hep b

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7
Q

What are the types of active vaccination?

A

Live attenuated vaccines
Killed and subunit vaccines
Vectored vaccines
Adjuvants

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8
Q

Goal of active vaccination

A

stimulating the
vaccinee’s immune system, to mount an adaptive
immune response to a specific pathogen

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9
Q

Describe live attenuated vaccines

A

May be attenuated form of virulent organism (eg. Measles, Sabin polio vaccine) or an
immunologically-related organism (eg. vacccinia)

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10
Q

Good things about live attenuated

A

Can still replicate - can spread to vaccines family

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11
Q

Bad things about live attenuated

A

Reversion to full virulence

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12
Q

Describe killed or ‘inactivated’ vaccines

A

May be whole organism, subunit, isolated toxins – antigen preparation chemically treated to
inactivate infectivity and toxicity

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13
Q

Describe whole organisms killed vaccines

Examples of whole organism killed vaccines

A

Heat or formaldehyde inactivated
shorter term immunity than attenuated vaccines (need boosters)
e.g. Cholera , Perussis

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14
Q

Describe subunit vaccines

Examples of subunit vaccines

A
  • antigenic viral surface components are isolated
  • these elicit a neutralising antibody response

Examples:
Influenza
Genetically engineered protein subunit from HBV
HPV

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15
Q

Example of inactivated exotoxin

A

Tetanus toxoid - need boost every 10 years

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16
Q

Describe conjugate vaccines

A

Antigenic polysaccharide from bacterial cell wall covalently-coupled (conjugated) to protein carrier
(eg. tetanus toxin); gives higher antibody titres than unconjugated polysaccharide vaccine
- Upon vaccination, the protein carrier provides peptides for MHC presentation, thus providing T cell
help for polysaccharide-specific B cells to make antibodies

17
Q

Describe toxoid vaccines

A

Inactivated derivatives of bacterial endotoxins (eg. diphtheria toxin, tetanus toxin – Clostridium
tetani)
- Rendered non-toxic by chemical (formalin) treatment or genetic engineering, but remain immunogenic

18
Q

Describe recombinant vaccines

A

Created via genetic engineering; the gene encoding a viral protein is inserted into a different, non-
pathogenic virus
- When the carrier virus replicates, the vaccine protein is produced, eliciting an immune response
- Examples are the hepatitis B vaccine, and human papillomavirus vaccine (HPV: a recombinant virus-
like particle is created in yeast, expressing single proteins of four different HPV strains, thus inducing
immunity to all four strains at once)

19
Q

MMR vaccine issues

A

 Adverse reactions, rarely serious – 10% of children develop fever, malaise, and a rash 5-21 days
after the first vaccination
 3% develop joint pain lasting on average 18 days
 Anaphylaxis is a rare but serious side effect
 Controversy: Andrew Wakefield, 1998 – MMR vaccine linked to autism and enterocolitis;
discredited, but led to decline in vaccination rates and increase in disease rates

20
Q

What are adjuvants?

A

Addition of substances that create a state of inflammation, helps stimulate effective immune
response