SciVaxx Flashcards

1
Q

How long does it take for antibody response when vaccinated?

A

→5-7 days

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2
Q

How long does it take for gull response when vaccinated?

A

→2 weeks

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3
Q

How long does it for full protective response when vaccinated?

A

→7 days

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4
Q

What type of response for polio?

A

→antibodies

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5
Q

What type of response for tuberculosis?

A

→cell mediated

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6
Q

Where does response have to be induced for influenza?

A

→mucosal sIgA

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7
Q

Where does response have to be induced for yellow fever?

A

→systemic

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8
Q

What is a parenteral vaccine?

A

→given by injection

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9
Q

What are oral vaccines processed by?

A

→mucosal associated lymphoid tissue (MALT) - good IgA production

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10
Q

What is the incubation period for cholera?

A

→short

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11
Q

Which antibody is found in breast milk?

A

→sIgA

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12
Q

What are monotypic pathogens?

A

→Surface antigens have remained the same to date.

→Vaccination or infection gives lifelong immunity

→eg. measles

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13
Q

What is antigenic drift?

A

→accumulation of mutations in genes that code for virus surface proteins with time

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14
Q

What is antigenic shift?

A

→recombination of viral strains to produce a different subtype with a mixture of surface antigens from the original strains

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15
Q

How are live attenuated vaccines made?

A

→serial culture in foreign host ‘passage’ e.g. Measles: 10 years of serial passage in tissue culture to transform wild virus into attenuated vaccine virus

→chemical mutagenesis and selection of phenotypes e.g Salmonella typhi TY21a

→genetic engineering to create knockouts lacking genes for virulence e.g. Vibrio cholerae

→Live attenuated vaccines can be useful for producing CTL memory cells as they can infect APCs

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16
Q

What are some dangers with live attenuated vaccines?

A

→reversion to virulence

17
Q

What do live attenuated vaccines require?

A

→cold chain to keep them alive

18
Q

How are inactivated organism vaccines made?

A

→Killed with heat or chemicals e.g. formalin or β-propiolactone

19
Q

What do killed vaccines require?

A

→booster for continued protection

20
Q

Examples of live attenuated vaccines

A

→BCG,
→polio
→MMR

21
Q

Examples for killed vaccines

A

→pertussis

→polio

22
Q

What are the types of subunit vaccines?

A

→- proteins (often surface antigen e.g. Hep B)

→ toxoids (diphtheria; tetanus)

→peptides (synthetic) e.g. M-001 Influenza vaccine being trialled
→polysaccharide poor antigens

23
Q

What molecules on bacteria is poorly recognised by children under 2?

A

→polysaccharide

24
Q

What are the disadvantages of bacterial capsular polysaccharides as vaccines?

A

→short term memory

→no T-cell immunity

25
Q

How is immunogenicity enhanced in capsular polysaccharides as vaccine?

A

→protein conjugation
→polysaccharide from bacteria and conjugate to a carrier protein
→taken into the cell and peptides presented to TH cell to produce antibody response and memory B cells

26
Q

Examples of capsular polysaccharide vaccines

A

→MenC

→Hib

27
Q

What are vaccine adjuvants?

A

→Chemicals added to vaccine to make them more immunogenic

→ promote uptake and antigen presentation

stimulate correct cytokine profiles

28
Q

Example of a vaccine adjuvant

A

→Aluminium salts (Alum
→form trapped particles (depot)
→slow release of antigen

29
Q

Why is it so difficult to produce a vaccine for HIV?

A

→High mutation rate

→Best way to do this is with an attenuated live vaccine but danger of reversion to virulence (especially with high mutation rate)

30
Q

What are passive vaccine treatments?

A

→Passive immunity: maternal transfer.

→Treatment with antibody from another source: serum

→Prophylaxis and/or treatment Rapid Short effect

31
Q

Describe rabies post exposure treatment

A

→injection with antibodies from serum of individuals who have been vaccinated against rabies into the wound site. HRIG – human rabies immunoglobulin