[3S] Vaccines Flashcards

(54 cards)

1
Q

VACCINE PREVENTABLE DISEASES

Introducing the antigen to a system; natural or induced.

A

Active Immunization

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2
Q

VACCINE PREVENTABLE DISEASES

Our own immune system is responsible for protecting us from a pathogen.

A

Active Immunization

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3
Q

VACCINE PREVENTABLE DISEASES

Protected from a pathogen by immunity gained from someone else.

A

Passive Immunization

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4
Q

Consists of antigen-induced formation of antibodies in the host and cell-mediated immunity.

A

Active Immunization

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5
Q

Requires time to develop → concurrent passive and active
○ Generally inactive at the time of specific exposure.

A

Active Immunization

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6
Q

Generally preferable to ____ immunization.
○ Higher antibody levels for longer periods of time
○ Less frequent immunization
○ Concurrent cell-mediated immunity

A

Passive

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7
Q

ACTIVE IMMUNIZATION

Duration of Immunity

A

Live vaccines > inactive vaccines

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8
Q
  1. Complete prevention of disease
  2. Prevention of the carrier state
  3. Production of prolonged immunity
  4. Absence of toxicity
  5. Mass immunization
    ● Inexpensive
    ● Easy to administer
  6. Easy transport
  7. Easy storage
A

Ideal Immunogen

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9
Q

Consists of transfer of immunity to a host using preformed immunologic products

A

Passive Immunization / Immunoglobulins

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10
Q

Only used for passive immunization due to the difficulty of passive administration of cellular components of the immune system and its association with graft-versus-host reactions.

A

Passive Immunization / Immunoglobulins

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11
Q

Interferons
○ Hematologic
○ Infectious diseases

A

Passive Immunization / Immunoglobulins

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12
Q

Confer temporary immunity

A

Passive Immunization / Immunoglobulins

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13
Q

○ Antibodies from mother to fetus during pregnancy.
○ Breast milk and colostrum.

A

Natural

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14
Q

CLINICAL USES

● Individuals unable to form antibodies.
● Prevention of disease when time does not permit active immunization - post-exposure.
● Treatment of certain diseases normally prevented by immunization.
● Treatment of conditions for which active immunization is unavailable or impractical.

A

Passive Immunization / Immunoglobulins

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15
Q

COMPLICATIONS

Absolute contraindication in passive immunization
○ May develop in individuals with certain immunoglobulin deficiencies.
○ Those with IgE deficiencies are at high risk.

A

Hypersensitivity reactions

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16
Q

● Have a shorter half-life (around 20 days).
● Anaphylaxis to serum sickness

A

Animal Antibodies

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17
Q

T/F: Anaphylaxis to serum sickness is least likely to happen with highly purified immunoglobulins (e.g. rodents or lagomorphs).

A

T

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18
Q

● Lower risk of hypersensitivity reactions.
● Much longer half-life in humans (IgG 23 days vs. 5-7 days.
● Smaller doses can be administered to provide therapeutic concentration for several weeks.

A

Human Antibodies

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19
Q

Preferred option for passive protection whenever
possible.

A

Human Antibodies

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20
Q

STORAGE

Inactivated vaccines
Diluents for lyophilized vaccines (or room temp.)
Live attenuated influenza vaccine nasal spray

A

Refrigerator 2-8°C

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21
Q

STORAGE

Lyophilized-powder live-virus vaccines

A

Freezer -15°C or colder

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22
Q

VACCINE TYPE

● Weakened virus
● Reduce virulence but retain immunogenic antigens.
● Humoral and cellular responses
● Memory cells: One or two doses

A

LIVE ATTENUATED VACCINES

23
Q

VIRUS

Measles Polio Rotavirus

A

LIVE ATTENUATED VACCINES

24
Q

VIRUS

Yellow fever
Chickenpox

A

LIVE ATTENUATED VACCINES

25
BACTERIA Vibrio cholera Tuberculosis
LIVE ATTENUATED VACCINES
26
DISADVANTAGES ● Must be refrigerated to retain their activity. ● Can mutate in the host virulent and cause disease.
LIVE ATTENUATED VACCINES
27
Contraindications of Live Attenuated
● Immunocompromised individuals ● Pregnancy
28
VACCINE TYPE ● Kill pathogens through: ○ Heat ○ Radiation ○ Chemicals ● Replicate or mutate (safe) ● Can be freeze-dried and transported without refrigeration.
INACTIVATED VACCINES
29
VIRUS Polio Influenza Rabies
INACTIVATED VACCINES
30
BACTERIA Typhoid Plague
INACTIVATED VACCINES
31
DISADVANTAGE ● Weaker immune response ● Multiple doses
INACTIVATED VACCINES
32
VACCINE TYPE ● Component of the microorganism ● Polysaccharides or proteins ● Considered safe because they have no live replicating pathogen present.
SUBUNIT VACCINES
33
VACCINE TYPE Includes: ○ Recombinant subunit vaccines ○ Hepatitis B
SUBUNIT VACCINES
34
DISADVANTAGES ○ Induce a less-robust immune system ○ Lengthy and costly to develop ○ Immunity is not guaranteed
SUBUNIT VACCINES
35
SUBUNIT TYPE ● Sugar antigens ○ Bacterial cell walls (peptidoglycan) ● Bacterial capsule polysaccharide ○ Carrier protein (diphtheria/tetanus toxoid)
Polysaccharide
36
SUBUNIT TYPE Meningococcal infection ■ Neisseria meningitidis - Group A, C, W-135, Y
Polysaccharide
37
SUBUNIT TYPE Haemophilus influenzae type b (Hib) Pneumococcal - PCV7, 10, 13
Polysaccharide
38
DISADVANTAGES ○ Not very immunogenic ○ Suboptimal immune responses (short-term immunity)
Polysaccharide
39
SUBUNIT TYPE ● T-protein-based: Purified proteins ● Includes: ○ Acellular pertussis (aP) ○ Hepatitis B vaccines (envelop protein)
Surface Protein
40
DISADVANTAGES ○ May not be presented in native form ○ Antibodies may not bind efficiently
Surface Protein
41
SUBUNIT TYPE ● Immune response bind and neutralize toxins. ● Prevents cell damage in the patient. ● Safe: No live pathogens ● Stable over a wide range of temperatures and humidities.
Toxoids
42
SUBUNIT TYPE Clostridium tetani Corynebacterium diphtheria
Toxoids
43
DISADVANTAGES Not highly immunogenic ■ Adsorbed to adjuvants (Al or Ca salts) to increase their capacity to stimulate the immune response.
Toxoids
44
VACCINE TYPE ● Antigenic genes: Synthetic DNA ● IM or ID ● APCs ● Both humoral and cellular
DNA VACCINES
45
No risk of infection Cost-effective Stable Long-term protection
DNA VACCINES
46
DISADVANTAGES ● Limit to protein antigens ● Tolerance to antigen (low immunogenicity)
DNA VACCINES
47
VACCINE TYPE Vector: Virus/bacterium ○ Microbial genes ○ Infects or transduces host cells ● The protein code are being packaged. ● Replaces the natural gene with microbial gene.
RECOMBINANT VECTORS
48
Includes: ○ Poxviruses (vaccinia) ○ Adenoviruses
RECOMBINANT VECTORS
49
VACCINE TYPE ● Developed quickly using the pathogen’s genetic code. ● Change the mRNA formulation to target a new antigen.
mRNA VACCINE
50
Non-replicating In vivo self-replicating In vivo dendritic cell non-replicating
RNA-Based
51
Tuberculosis Oral polio vaccine (OPV) Measles Rotavirus Yellow fever
Live Attenuated (LAV)
52
Whole-cell pertussis (wP) Inactivated poliovirus (IPV)
Inactivated
53
Acellular pertussis (aP) Hib Pneumococcal (PCV-7/10/13) Hepatitis B
Subunit
54
Tetanus toxoid (TT) Diphtheria toxoid
Toxoid