Vaccines Flashcards

1
Q

What is the difference between Innate & Adaptive immunity?`

A
Innate Immunity:
- Basic resistance to disease (immunity)
- Provides immediate protection
- Same response regardless
- No memory
(Eg. Phy barriers (Skin/mucosa), Physiologic factors (Gastric acid), Process (Inflmm), Cells of immune system)

Adaptive Immunity:

  • Protection develops more slowly (days)
  • Developed after exposure to antigen
  • Effective only against specific antigen
  • Has memory (enhanced ability to deal with recurring antigen)
  • -> Upon 1st exposure, developement of pri immune response with proliferation of activated B cells & T cells into effector cells, and some to memory B & T cells
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2
Q

LO1: How do vaccines elicit an immune response & provide protection?

A
  • Prime the adaptive immune system to provide a long-lasting targeted response that prevents infection
  • By memory from the Adaptive Immunity (Basis of vaccination)
  • -> Activation of memory cells –> Secondary response with shorter lag time between exposure & production of response + Heightened state of activity
  • -> Faster & stronger immune response
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3
Q

What does it mean by ‘Vaccination is a form of active immunization’

A

Provide immunization before host even comes into contact with the pathogen

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4
Q

LO2: Characteristics & distinctions of LIVE VACCINES

A

What: Weakened virus, often by repeatedly passing through tissue culture in which it replicates poorly

  • > Immunogenic: Activates killer T Cells
  • 1/2 doses can provide lifelong immunity
  • Temp-sensitive: Must be refrigerated
  • < safe for people with weakened immune system
  • Need to be given spaced apart from other live vaccines
  • Not generally given to infants

Eg: Measles, mumps, rubella, varicella, rotavirus

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5
Q

LO2: Characteristics & distinctions of INACTIVATED VACCINES (non-living)

A

What: Inactivated by treating with heat/chemicals to kill it

  • Easy to store & transport
  • Low risk of causing infection
  • Elicits weaker immune response
  • May require several doses/boosters to attain adequate response

Eg: Polio, Rabies, Hep A

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6
Q

LO2: Characteristics & distinctions of SUBUNIT VACCINES (non-living)

A

What: One/more parts of the pathogen are isolated & used to evoke an immune response

  • Low risk of causing adverse reaction
  • Can be used in people with weakened immune systems
  • Can be difficult to manufacture
  • May require boosters to attain adequate response

Eg: Hep B, Influenza, Pertussis Pneumococcus

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7
Q

LO2: Characteristics & distinctions of TOXOID VACCINES (non-living)

A

What: Toxin produced by pathogen is deactivated & used to produce the immune response

  • Unable to cause disease/ spread
  • Stable, easy to distribute
  • May require boosters to maintain immunity

Eg: Diphtheria, tetanus

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8
Q

LO2: Characteristics & distinctions of RECOMBINANT VACCINES (non-living)

A

What: Produced using genetic engineering. May contain no actual virus/ modified strain of virus (as with live oral typhoid)

Eg: Hep B, HPV

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9
Q

Precautions with live vaccines

A
  • Avoid in pregnancy/ severely immunocompromised
  • -> Concern for uncontrolled replication -> Cause actual clinical infection
  • Not usually given to infants
  • Avoid giving another live vaccine within 28 days
  • Space 3-10 mths apart from other ab-containing products
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10
Q

LO3: List vaccines available for infections transmitted by RESPIRATORY route

A
  • Influenza
  • Pneumococcus
  • Meningcoccus
  • H. influenzae
  • BCG (Tuberculosis)
  • MMR (Measles,Mumps,Rubella), Chickenpox
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11
Q

LO3: List vaccines available for infections transmitted by FOOD & WATER route

A
  • Hep A
  • Typhoid
  • Cholera
  • Rotavirus
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12
Q

LO3: List vaccines available for infections transmitted by VECTOR-BORNE route

A
  • Yellow fever

- Jap Encephalitis Dengue

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13
Q

LO3: List vaccines available for infections transmitted by BLOOD & BODILY FLUIDS route

A
  • Hep B

- HPV

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14
Q

LO3: List vaccines available for infections transmitted by CONTACT route

A
  • Tetanus
  • Rabies
  • Shingles
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15
Q

LO4: Describe principles of Herd Immunity

A

High vaccination rate in population such that most community members are protected, even the unimmunized individuals

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16
Q

What is the diff between Primary & Booster dose?

A

Pri: Single/Few doses
Booster: Additional dose of vaccine to maintain protective levels of antibody

17
Q

LO5: List vaccines in NCIS

A
  • BCG
  • Hep B
  • DTap
  • Tdap
  • MMR
  • VAR
  • IPV
  • Hib
  • INF
  • PCV10/PCV13
  • HPV2/HPV4
18
Q

LO5: List vaccines in NAIS

A
  • Hep B
  • MMR
  • VAR
  • HPV (Females 18-26yo)
  • Tdap (1x during each pregnancy)
  • INF (1x anually/season for >65yo or if have indication)
  • PCV13 & PPSV23 (1x for >65yo or if have indication)
19
Q

LO6: Discuss the general considerations for vaccine use

Effectiveness & Adverse Effects

A
  • Effectiveness (Varies by vaccine)
  • Site vaccine given (Eg. Hep A/B IM in deltoid, not gluteus)
  • Patient age & immune status
  • Cold chain problems

Adverse effects:
Common - Pain @ inj site, headache, myalgia
Uncommon - Fever, hematoma
Rare (Severe) - Anaphylaxis, Hypersensitivity

20
Q

LO6: Discuss the general considerations for vaccine use

Contraindications & Precautions

A
  • Allergy
  • Moderate/severe illness (Fever > 38C)
  • Bleeding risk (Caution with administration)
  • Pregnancy (Live vaccines)
  • Immunocompromised (Live vaccines)
21
Q

LO6: Discuss the general considerations for vaccine use

Simultaneous administration & Missed Doses

A
  • Mostly no problem
  • EXCEPTION: PCV vaccine & meningcoccal conjugate vaccine shld be given 4 weeks apart for pts with functional/anatomical asplenia
  • Missed dose: Dose given as soon as possible
22
Q

LO7: Other components in vaccine

A

1) Stabilisers (Sorbitol, Mg Sulfate)
- To ensure components stable & effective

2) Preservatives (Thiomersal)
- Prevent contamination

3) Adjuvants (Al hydroxide/phosphate)
- Enhance body’s immune response
- Thought to help keep antigens near site of injection (?)

4) Antibiotics (Gentamicin, Neomycin)
- Prevent bacterial contamination
- Later removed, only residual qty remain after production process

5) Trace components (Formaldehyde)
- Left-over from production