Immunisation Flashcards

1
Q

Name the types of vaccines used

A

Whole killed, toxoids, live attenuated

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2
Q

Name the types of immunisation

A

Passive immunisation

active immunisation or vaccination

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3
Q

Define passive immunisation

A

The administration of pre-formed immunity from one person or animal to another person

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4
Q

Passive immunisation advantages, limitations and disadvantages?

A

Advantages - gives immediate protection, effective in immunocompromised pts

Disadvantages - short lived, possible transfer of pathogens, serum sickness on transfer of animal sera

Limitation - antibody mediated

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5
Q

Examples of passive immunisation?

A

Specific immunoglobulin;

  • Human tetanus immunoglobulin = rapid protection
  • Human rabies specific Ig = after rabies exposure to give protection until vaccine effective
  • Human hepatitis B Ig
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6
Q

Passive immunisation backup - Normal immunoglobulin?

A

From pools of at least 1000 donors, contains antibody against measles, mumps, hepatitis A
Done in emergencies

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7
Q

What is active immunisation?

A

Vaccination - divided into:

  • Non-living vaccines
  • Live attenuated vaccines
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8
Q

What are non-living vaccines?

A

The memory immune response
1st response = IgM
2nd exposure to antigen = larger immune response as memory B cells work = mainly IgG

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9
Q

What are whole killed vaccines?

A

Bac or viruses grow in vitro and inactivated using an agent e.g. formaldehyde

  • Non-living vaccine does not cause infec, but antigens cause an immune response that protects against infection
  • Can also be cell-free toxoids-inactivated toxins
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10
Q

Limitations of whole killed vaccines?

A
  • Organism must be growth to high titre in vitro
  • Whole pathogens often cause excessive reactogencity
  • Immune response are not always close to normal response to infec
  • Need at least 2 shots
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11
Q

Examples of non-living vaccines?

A

Bacterial;

  • Diptheria-cell free formaldehyde treated toxin = rendered non-toxic
  • Tetanus, toxoid
  • Cholera - heat killed bac

Viral;

  • Polio vaccine - inactivated virus - IPV
  • Influenza vaccine - inactivated virus
  • Hepatitis A vaccine - inactivated virus
  • Rabies vaccine - inactivated virus
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12
Q

What are live attenuated vaccines?

Define attenuation?

A

Organisms replicate within the host
Induce immune response = protective against the wild-type organism
More protective

Attenuation = Organism is cultured in such a way that it does not cause disease when inoculated into humans

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13
Q

Advantages of live attenuated vaccines?

A
  • Lower doses required, so the scale of in virto growth needed is lower
  • Immune response more closely mimics that following renal infection
  • Route of administration may be more favourable
  • Fewer doses may be required
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14
Q

Limitations of live attenuated vaccines?

A
  • Often impossible to balance attenuation and immunogenicity
  • Live vaccines may not be so attenuated in immunocompromised hosts
  • Transmissibility?
  • Reversion to virulence?
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15
Q

Examples of live attenuated vaccines?

A

Bacterial;

  • BCG - Myobacterium bovis grown over many passages in vitro - gives some protection against TB
  • Salmonella typhi - temp sensitive strain given orally

Viral;

  • Poliomyelitis - bring polio to brink of eradication
  • Measles, mumps and rubella - 3 given together
  • Vaccina virus - eradicate smallpox
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16
Q

Examples of pathogens lacking vaccines?

A

HIV, malaria, Herpes simplex virus, CMV

17
Q

Why do so many pathogens lack vaccines?

A
  • Pathogen too hard to grow
  • Killed pathogen not protective
  • Impossible to obtain attenuated and suitability immunogenic strain
  • Too many strains causing disease
18
Q

Novel approaches?

A

Recombinant proteins, synthetic peptides, live attenuated vectors, DNA vaccines

19
Q

How are recombinant proteins formed?

Examples of recombinant proteins?

A

Produced from bac, yeast, inset or mammalian cells

- Hep B surface antigen, HPV vaccines cervarix

20
Q

Recombinant protein benefits and negatives?

A
Benefit = Avoid problem of having to grow pathogen in vitro
Neg = Major difficulties are finding protective protein(s) and generating a strong immune response
21
Q

Synthetic peptides pos and negs?

A
  • Avoid need to pathogen growth

Negs;
- Identifying protective epitopes and inducing a strong and broad response is a problem

22
Q

Live attenuated vectors?

A

Express protein from the pathogen in a vector which is know to be attenuated and safe
e.g. Vaccina, BCG
Potential problems in immunodeficient people

23
Q

How do live attenuated vectors work?

A

= Attenuated, genetically stable vaccine

  • Vector able to take additional foreign DNA
  • Insert DNA encoding protective antigen of pathogen e.g. HIV
24
Q

How do DNA vaccines work?

A

Express protein from the pathogen in a mammalian expression plasmid which is then injected = protein is expressed

25
Q

Pros and cons of DNA vaccines?

A
  • Avoid need to grow pathogen
  • No live organisms involved
  • Cheap

Neg = poor immunogenicity

26
Q

T independent antigens?

A

Bacterial capsular polysaccharides cannot be processed + presented on MHC class II = No T cell help
Antibody response of low magnitude
Low affinity
Predominantly IgM
Little or no boosting on secondary exposure
Infants respond especially poorly and are major target group for these vaccines
e.g. Haemophilus influenzae
Neisseria meningitidis
Streptococcus pneumoniae

27
Q

Conjugation of TI antigens to proteins?

A
  • Hib polysacc specific B cells bind polysaccharide and internalise whole conjugate, including protein
  • Polysaccharide cannot be processed, but protein is and peptides derived from it are expressed on cell-surface with MHC class II
  • Polysaccharide specific B cell receives help from DT specific T cell
  • Strong antibody response even in infants, including IgG
28
Q

Examples of conjugate vaccines?

A
  • Neisseria meningitidis type C- polysaccharide-protein conjugate vaccine
  • Streptococcus pneumoniae-23-valent polysaccharide vaccine or 7-valent conjugate
  • Haemophilus influenzae type B (HiB)- Polysaccharide protein conjugate vaccine
29
Q

Recent changes to childhood immunisation programme?

A

The addition of a pneumococcal conjugate vaccine (PCV) at 2, 4 and 13 months of age;

A dose of MenC vaccine at 3 and 4 months;

A booster dose of Hib and MenC vaccine (given as a combined Hib/MenC vaccine) at 12 months of age.

HPV vaccine for teenage girls

BCG no longer routinely given to teenagers. Targeted on at risk infants.

30
Q

Do vaccines work?

A

Diptheria - 5 died since vaccine = 99.99% change

Polio - 0 died since vaccine = 99.98% change