Immun Flashcards

1
Q

How many types of immunity are there?

A

Innate and Acquired

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2
Q

Innate Immunity involves

A
Physical barriers
Physiological factors (pH, temp, stomach acid)
Protein secretions
Inflammation process and
Macrophages
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3
Q

Macrophages

A

Recognize antigen as foreign, engulf it, break it down, and deliver it to helper T cells which release cytokines

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4
Q

Acquired Immunity involves

A

cells circulating from prev exposures (T cells and B cells)

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5
Q

T cells offer

A

cellular immunity

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6
Q

T cells come from

A

the thymus

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7
Q

Types of T cells

A

Helper T cells and Cytotoxic T cells

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8
Q

Helper T cells

A

attach to antigen and release cytokines (messengers) which generate a B-cell response

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9
Q

Cytotoxic T cells

A

attaches to antigen and destroys it

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10
Q

B cells offer

A

humoral immunity

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11
Q

B cells come from

A

bone marrow

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12
Q

B cells

A

mature to antibody producing cells (plasma cells)

and some cells remain circulating (as memory cells)

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13
Q

Plasma cells

A

which produce antigen-specific antibodies that attach to antigen and mark it for destruction

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14
Q

Memory cells

A

activate immune response upon re-exposure to antigen. Rapidly produces antibodies which eliminate antigen.
They may wane over time.

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15
Q

Vaccines and the Immune response

A

Vaccines contain antigens which are recognized by the immune system and evoke an immune response

B cells and T cells are activated

T cell activation also leads to B cell activation and B cell activation results in the production of antibodies which mark antigens for destruction.

The antigen is eliminated and Memory B and T cells are formed

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16
Q

Vaccine Types

A

Live attenuated and Inactivated

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17
Q

Both vaccine types are made from

A

viruses or bacteria

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18
Q

Live attenuated vaccines

A

made from whole virus or bacteria.

must replicate to work. Replication mimics natural infection, which stimulates an immune response

19
Q

Inactivated vaccines

A

can be made from various fractions of virus or bacteria

They do not replicate because they are killed - the antigen load stimulates immune response

May contain adjuvants to enhance immune response

20
Q

Polysaccharide vaccines

A
  • b cells stimulated w/out use of helper t cells

- short-lived, no booster effect, not consistently immunogenic in children < than 2 yrs

21
Q

Conjugate polysacc vaccines

A
  • helper t cells involved, memory cells produced, booster effect upon subsequent exposure, inc immunogenicity in children < 2 yrs
22
Q

Two live vaccines if not simultaneous

A

28 day separation

23
Q

Live vaccines followed by blood products

A

2 week separation

24
Q

Blood product given before live vaccine

A

interval varies

25
Q

Live vaccine followed by PPD skin test

A

28 day separation

26
Q

PPD skin test followed by live vaccine

A

administer vacc after PPD skin test has been read

27
Q

If the int between vaccine doses in a series is dec

A

may interfere with antibody response and protection

28
Q

if the int between vaccine doses in a series is inc

A

doesn’t reduce vacc effectiveness but delays protection for the patient

29
Q

contraindication

A

condition that greatly inc the risk o/ an adverse rxn

30
Q

general rule for contraindications

A

do not vacc if vacc likely to injure patient

31
Q

Universal contraindication for all vaccines

A

severe allergic response to a previous dose

32
Q

False contraindications

A
minor illness
allergies to prods not in vacc
allergies that are not immed &amp; life threatening
pregnancy in the household
breastfeeding
premature birth
33
Q

Is it ok to get multiple vaccines in one day

A

yes - immune system designed to handle it

34
Q

Vaccines and pregnancy

A
  • encourage vaccines prior to or after pregnancy
  • only inac flu vacc during pregnancy if pregnant during flu season, and Tdap for every pregnancy (after 20 weeks gestation)
35
Q

Vaccines in Immunosuppressed individuals

A

live vaccines usually not recommended

concern with inactivated vaccines not being effective enough

36
Q

Gen guidelines for immunosupp

A

vaccines 4 weeks prior to immunosupp

healthy indiv who reside in a household with patients can receive inac and most live vacc with cautions in place

37
Q

Min interval on catch up sched

A

28 days for most

38
Q

Administration slightly earlier

A

unlikely to interfere with antibody production

39
Q

grace period for sequential dosing of series

A

4 days - can be administered < or = 4 days before min int

40
Q

grace period applies to

A

same-antigen live vaccs

41
Q

grace period does not apply to

A

diff live vaccs (MMRV or MMR and varicella)

42
Q

_ do not have interval rules

A

oral live vaccs (typhoid and rotavirus)

43
Q

does a vaccine series ever have to be restarted

A

No