19--Practical Immunology Flashcards

1
Q

use ___ assays to exploit Ab-Ag interaction for detection of Ab or Ag

A

serological

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2
Q

what is ELISA?q

A

Enzyme linked immunosorbent assay

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3
Q

how does ELISA work?

A

1) Ag attached to solid support 2) patient serum added–Ab bind to antigen 3) add second Ab (anti-human Ig) which recognizes human Ig and is tagged with enzyme 4) add substrate for tagged enzyme (coloured rxn product is produced if anti-human Ig has bound to Ab-HCV complex)

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4
Q

positive ELISA result means:

A

Ab against certain micro org present in patient serum

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5
Q

what is window period?

A

between first contact w/ microbe and time which first Ab appear (days to weeks)

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6
Q

important tests using antibody-capture ELISA?1

A

pregnancy (free monoclonal Ab specific for hCG)

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7
Q

what is agglutination test used for?

A

discrimnate tween closely related strains of same spp (serotypes)

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8
Q

drugs that stim production of lymphocytes in bone marros (purified cytokines)

A

immunostimulatory drugs

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9
Q

methotrexate is ex. of _____

A

immunosuppressive drug

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10
Q

studied nutr for immunity?

A

zinc, selenium, copper, vits, folic acid

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11
Q

___ in broccoli may boost immune sys

A

DIM (good for ^ cytokines and WBC)

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12
Q

Cold FX claims supported by sci?

A

effects on innate immunity (^ macrophage), fx on acquired immunity (^ cyto and B cells)

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13
Q

evidence for probiotics prevention of cold?

A

noooo

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14
Q

think ___ instead of “boost” IS

A

maintain

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15
Q

principle of vaccines:

A

induce memory B/T cells against microbe so future exposure result in rapid immune response which will eliminate before cause disease

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16
Q

temporary short term immunity that results when Ab admin to person

A

passive immunization

17
Q

examples of passive?

A

immune globulin (prepared from blood of donors w/ high lvl Ig against certain pathogens–>3 wks), maternal Ab (4-6months)

18
Q

longer term immunity due to immune response following exposure to Ag

A

active immunization (vaccines)

19
Q

two types of vaccines

A

whole cell and sub-unit (acellular)

20
Q

why risks of adverse rxn in whole cell?

A

toxic bacterial comps still present (inflammation, fever)

21
Q

ex. of whole cell vaccines?

A

polio, cholera

22
Q

ex. live attenuated whole cell?

A

measles, mumps, rubella

23
Q

how does live attenuated whole cell work?

A

multiply briefly in host but can’t cause disease (cuz of mutations), most closely mimics natural infection so has lifelong immunity

24
Q

slight risk of ___ in live attenuated whole cell

A

back mutation to original non-attenuated microbe

25
Q

ex. of subunit vaccines?

A

whooping cough, diphtheria, tetanus

26
Q

pros of subunit vaccines?

A

fewest advers side effects

27
Q

cons subunit vacc?

A

less likely produce cell mediated immunity, less likely life-long (need booster)

28
Q

most vaccines include ____ to enhance immune response

A

“adjuvants”

29
Q

example of adjuvant?

A

aluminum sulfate, squalene, saponin

30
Q

how do adjuvants work?

A

trap antigen for more sustained/slow release, combine w/ antigen for more efficient activation of T cells, non-specific immune stim. (good for sub-unit vaccines)

31
Q

protection achieved by being part of larger grp that includes lots of immunized ppl

A

herd immunity

32
Q

oral poliovirus vaccine replaced by:

A

salk

33
Q

challenges in vacc development?

A

bundling, finding right one that doesn’t cause probs, better life-long, stability under adverse conditions, improve delivery systems, get people on board with getting vaccines, old diseases keep vaccinating