Ch 17 Infectious Diseases and Vaccines Flashcards

1
Q

Emerging Disease

A

something new, not previously observed

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2
Q

example of an emerging disease

A
  • New strains of influenza

- SARS-CoV-2

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3
Q

Re-emerging disease

A

something old, coming back again

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4
Q

example of a re-emerging disease

A

measles in the US

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5
Q

What factors can increase the likelihood of emerging diseases?

A
  • increases in international travel
  • mass distribution of contaminated food
  • improper antibiotic use
  • spread of humans into previously uninhabited areas, introducing to novel microbes
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6
Q

What factors can increase the likelihood of re-emerging diseases?

A
  • combinations of diseases (HIV and TB)

- laxity in vaccination program adherence

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7
Q

Example of re-emergence combinations of diseases

A

HIV and TB

  • in the 90s, it was thought that TB would soon disappear as a problem in the US
  • the AIDS epidemic resulted in a large increase in immunocompromised individuals, who subsequently became sick with Mycobacterium
  • regular treatment of immunocompromised patients with antibiotics resulted in resistant TB strains
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8
Q

Example of re-emergence of disease due to laxity in vaccination program adherence

A
  • diptheria in Soviet Union
  • Whooping cough in US
  • Measles in US
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9
Q

Passive immunization

A

delivery of preformed antibody

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10
Q

Protective immunity can be achieved by ___ or ____ immunization.

A

active;passive

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11
Q

Conditions that warrant passive immunization

A
  • immune deficiency
  • toxin or venom exposure with immediate threat to life
  • exposure to pathogens that can cause death faster than an effective immune response can develop
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12
Q

Why can passive immunization lead to Type I or III hypersensitivities?

A

Ab agents are typically made from animals

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13
Q

What is the goal of vaccination?

A

to provide a primary exposure to a safer form of an antigen, either by exposing to a protein/polysaccharide or by exposure to a weakened (attenuated) form of the pathogen

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14
Q

The goal of vaccination is to provide a ____ ______ to a safer form of an antigen.

A

primary exposure

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15
Q

Vaccinations provide _____ ______ without the potential negative consequences of a natural infection.

A

active immunity

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16
Q

Side effects of vaccines, when present, are usually indicators of ____ _____ to a novel pathogen

A

immune reaction

17
Q

Herd immunity

A

resistance to the spread of an infectious disease within a population that is based on pre-existing immunity of a high proportion of individuals as a result of previous infection or vaccination

18
Q

Basic reproductive number values

A

the infectibility of a disease

19
Q

Simplified calculation for finding the percentage of people that need active immunity against an agent to achieve herd immunity is based on the:

A

basic reproduction number (R0) of the agent

20
Q

How do you calculate the approximate level of herd immunity required based on the R0 value?

A

Herd immunity= 1 - 1/R0

21
Q

Once a vaccine is approved, what other safety measures are in place to ensure that vaccine is still as safe as possible?

A

after approval by the FDA, every lot of vaccine must be tested before release and manufacturing facilities are checked regularly for compliance of safety and manufacturing procedures

22
Q

Live attenuated vaccine components

A

pathogens are weakened by continuous growth in conditions outside of their ‘ideal’

23
Q

Pros of live attenuated vaccines

A
  • retain their ability to replicate, promoting both humoral and cell-mediated responses
  • often do not need boosters
24
Q

Cons of live attenuated vaccines

A
  • may mutate back (revert) to pathogenic form
  • may have more side-effect complications
  • may also require a “cold chain” for stability during transport
25
Q

Inactivated vaccine components

A

heated or chimically treated to inactivate pathogen

26
Q

Pros of inactivated vaccines

A
  • no reversion to pathogenic form

- often more stable/easy to store and transport

27
Q

Cons of inactivated vaccines

A
  • require booster shots
  • don’t replicate in host, so often don’t induce cell-mediated immunity well (humoral only)
  • possible chemical exposures/adjuvants often required
  • potentially dangerous if not all pathogen is killed/inactivated
28
Q

Subunit vaccine components

A
  • use purified macromolecules derived from pathogen
  • inactivated exotoxins/toxoids
  • inactivated capsular polysaccharides
  • inactivated surface glycoproteins (or recombinant protein Ag_
29
Q

Pros/cons of subunit vaccines

A

similar to those of innactivated vaccines

30
Q

Conjugate/multivalent subunit vaccines

A

some molecules aren’t strong enough Ags on their won to stimulate a good response

  • couple them with something else that is (conjugate)
  • deliver them in a mixture of proteins (multivalent)
  • have to deliver Ag into cells for presentation in MHC I