Lecture 8- Defence and Vaccination against Bacteria Flashcards

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1
Q

What are the different forms of bacterial vaccines?

A
  • Toxoids
  • Conjugates
  • Live attenuated
  • Killed whole cells
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2
Q

What are the two different types of immunities and briefly compare them

A

1) Innate
- first line defence
- rapid
- not very specific (molecular patterns)
- does not require previous expose
- Monocytes and PMLs
- inflammatory
2) Acquired
- takes time
- requires previous exposure
- Lymphocytes (+ other cells involved)

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3
Q

What are the two subclasses of of acquired immunity?

A

1) Humoral
- antibodies
- produced by B lymphocytes
- Plasma cells secret Igs
2) Cell Mediated
- T lymphocytes and NK cells
- involvement of other cells (macrophages)

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4
Q

What are the roles of antibodies?

A
  • Opsonisation
  • Agglutination
  • Neutralisation (of toxins)
  • Complement activation
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5
Q

What are the roles of cell-mediated immunity?

A
  • For intracellular pathogens

- Interaction of T lymphocytes and macrophages

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6
Q

What are the properties of a good vaccine?

A
  • stimulates an effective immune response
  • safe and no adverse reaction
  • inexpensive
  • stable
  • easy to administer
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7
Q

Define the term ‘herd immunity’

A

The effect of immunity within a population where enough people are immune, protecting those who are still susceptible to the disease.

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8
Q

What happens in the different phases of clinical trials?

A

PHASE 1- test for safety and immunogenicity. In a small number of healthy adults
PHASE 2- assess immune response, safety. In small target group
PHASE 3- Placebo controlled double blind trials, check effectiveness.

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9
Q

How do you calculate vaccination efficacy?

A

1 - (Attack rate in vaccinated group/ attack rate in unvaccinated group)
- expressed as a %

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10
Q

During which phase of the clinical trials is vaccination efficiency determined?

A

Phase III

blinded placebo controlled stage

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11
Q

How do you calculate the vaccine coverage needed to achieve the herd effect?

A

(1-1/R0)/ effectiveness

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12
Q

How do you calculate the herd effect?

A

1- (attack rate unvaccinated post-intro/ attack rate unvaccinated pre-intro)

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13
Q

What three things do vaccines contain?

A

1) Antigen- to stimulate the immune response to the target disease
2) Adjuvant- to enhance and modulate the immune response
3) Excipients- buffer, salts, saccharides, protein to maintain pH, osmolarity and stability of the vaccine and preservatives

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14
Q

How do DNA vaccines result in immunity?

A
  • DNA is entered
  • host expresses the desired antigen
  • host mounts its own immune response
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15
Q

What sort of vaccine is DTaP?

A

Tetanus and Diptheria are toxoids= chemically inactivated bacterial exotoxins

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16
Q

What are the advantages of a toxoid vaccine?

A
  • Simple to produce
  • relatively pure
  • safe
  • high protective efficacy
    • very immunogenic
    • appropriate immune response (toxin neutralising antibodies block activity)
17
Q

What is the aP of DTaP?

A
  • pertussis
  • infects ciliated epithelium and releases toxins
  • convulsive cough
  • recovery after antibody production
18
Q

What type of vaccine is the pertussis vaccine?

What are the pros and cons of the vaccine?

A
Whole cell vaccine 
PROS: efficacy rate > 90%
CONS:
- anaphylaxis
- prolonged crying
- febrile seizures
- acute encephalopathy (caused by Na+ channel mutations)

Can also get acellular vaccine

19
Q

Which components of B. pertussis is associated with virulence?

A

1) Attachment to ciliated epithelium
2) Adherence and complement resistance
3) Toxins (pertussis toxin)

20
Q

What is His? What are its symptoms? What sort of vaccine is it?

A

H. influenza type B
- meningitis
- septicaemia
Conjugate vaccine

21
Q

What is the paediatric combination vaccine called? Which antigens does it protect against? What is it adjuvant?

A

VACCINE:
= DTaP- Hib- IPV

ANTIGEN:

  • Diptheria toxoid
  • Tetanus toxoid
  • acellular Pertussis components ( pertussis toxoid, filamentous haemagglutinin, pert actin, fibrine t2/3)
  • Hib PRP- conjugate
  • Inactivated polio virus types 1,2 and 3

ADJUVANT: aluminium phosphate

22
Q

What is the structure of polysaccharide antigens?

A
  • large and linear
  • not readily degraded
  • highly repetitive determinant
23
Q

What is the immune response to a polysaccharide antigen?

A
  • predominantly IgM
  • poor memory effect
  • low avidity antibody
  • T cell independent antigen
24
Q

What are conjugate vaccines?

A

Carbohydrate chemically linked to an immunogenic protein

25
Q

What are the pros and Cons of conjugate vaccines?

A

PROS: highly purified components= safe, simple for licensure and control, effective long-lived bootable immunity, offer herd immunity
CONS: sophisticated technology= expensive