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
Live vaccine followed by PPD skin test
28 day separation
26
PPD skin test followed by live vaccine
administer vacc after PPD skin test has been read
27
If the int between vaccine doses in a series is dec
may interfere with antibody response and protection
28
if the int between vaccine doses in a series is inc
doesn't reduce vacc effectiveness but delays protection for the patient
29
contraindication
condition that greatly inc the risk o/ an adverse rxn
30
general rule for contraindications
do not vacc if vacc likely to injure patient
31
Universal contraindication for all vaccines
severe allergic response to a previous dose
32
False contraindications
``` minor illness allergies to prods not in vacc allergies that are not immed & life threatening pregnancy in the household breastfeeding premature birth ```
33
Is it ok to get multiple vaccines in one day
yes - immune system designed to handle it
34
Vaccines and pregnancy
- 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
Vaccines in Immunosuppressed individuals
live vaccines usually not recommended | concern with inactivated vaccines not being effective enough
36
Gen guidelines for immunosupp
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
Min interval on catch up sched
28 days for most
38
Administration slightly earlier
unlikely to interfere with antibody production
39
grace period for sequential dosing of series
4 days - can be administered < or = 4 days before min int
40
grace period applies to
same-antigen live vaccs
41
grace period does not apply to
diff live vaccs (MMRV or MMR and varicella)
42
_ do not have interval rules
oral live vaccs (typhoid and rotavirus)
43
does a vaccine series ever have to be restarted
No