Vaccinations Flashcards

1
Q

What might an ideal vaccine might have

A
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2
Q

How does vaccination work on immune system

A

Prevention of entry - antibodies (neutralisation, opsinisation)

Killing infected cells (CD8

Boosting immune response (CD4 T cells MHC moelcule, make Ig)

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3
Q

What is the R0

A

Number of cases on case generates over the cause of infection period

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4
Q

What are the different types of antigens in vaccination

A

Inactivated protein e.g. tetanus toxoid

Recombinant protein e.g. HepB

Live attenuated pathogen e.g. Polio/BCG

Dead Pathogen e.g. split flu vaccine

Carbohydrate e.g. S pneumoniae

Adjuvant - make vaccine work better

Stabilising agent - buffer

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5
Q

Inactive toxoid vaccines

A

Tetanus toxoid

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6
Q

Recombinant Portein Vaccines

A

Hep B Surface Antigen

Recombinant protein from pathogen

Induces classic neutralising antibodies

Pure and safe

Relatively expnesive, not very immunogenic, not answer to all infections

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7
Q

What is wrong with this structure

A

Antibodies are made against 2nd structure instead of first structure

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8
Q

Whats the problem with bacterial coats

A

Have a capsule made of polysaccharide

Not good at inducing a B cell response (T independent antigen)

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9
Q

Conjugates vaccines

A

S pneumoniae

T cell recognises protein (immunogenic carrier protein)

B cell recognise sugar part

Advantage: imporves immunogenicity, highly effective at controlling bacterial infection

Disadvantage: cost, carrier protein intereference, strain specific, polysaccharide alone is poorly immunogenic

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10
Q

Dead pathogen vaccines

A

Influenza

Induces antibody and T cell response

Leaves antigenic components intact. Immunogenic because of the inclusion of other components. Cheap. Quick

Fixing/killing can alter antigen strucutre, dirty, capacity to grow pathogen,

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11
Q

What is live attenuated vaccines

A

BCG, LAIV, OPV

Pathogens are attenuated by serial passage, loss of virulence

Because they replicate in situ, trigger innate response and boost immune response

Induce strong immune response, can induce a local immune response in site where it occurs

Disafvantages: virulence, can infect immunocompromised, attenuation may lose key antigens, competed out by other infections

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12
Q

What are adjuvants

A

Substances used in combination with a specifi antigen that produced a more robust immune response than antigen alone

Induce danger signals that activate dendritic cells to present antigen to T cells

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13
Q

Types of adjuvants

A
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14
Q

Vaccine barriers

A

Scientific challenges

Injection safety

Time, cost

Public risk free expectation

Logistics/ cold chain

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15
Q

High variation of the target orgnaisms

A

Immune response will only recognise one of the strains

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16
Q

Phases of clincal trials

A

Phase 1 - safety in humans

Phase 2 - safety and efficacy

Phase 3 - More participants

17
Q

How are new vaccines are introduced into the UK schedule

A

Recommended - JCVI

Vaccine policy - DH

Licensing - MHRA

Purchase - DH

Control of vaccine (NIBSC)

Post licensure assessment and changes (PHE/JCVI)

18
Q

Scheduling

A
19
Q
A