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Unit I - Immune System (Part 1) Flashcards

(38 cards)

1
Q

innate immunity

A

body’s first line of defense to prevent entry of pathogens; present at birth

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2
Q

2 basic systems of innate immunity

A
  1. skin/mucosal barriers

2. inflammatory response

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3
Q

acquired immunity

A

body’s immune system to recognize and inactivate foreign substances without injury to other host tissue

  • occurs after exposure to a foreign substance after birth
    ex) breast feeding, infections
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4
Q

innate immunity also utilizes

A

natural killer (NK) lymphocytes

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5
Q

function of natural killer (NK) lymphocytes

A

surveillance
recognize abnormal cells and kills them
secrete performs and Granenzymes

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6
Q

factors that activate natural killer (NK) lymphocytes

A

cytokines, FcR molecule for Fc antibodies, FcR receptor (see pg 12)

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7
Q

cells for defense - foreign invaders

A

T and B lymphocytes

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8
Q

passive immunity

A

acquired by receiving antibodies from another person

ex) breast feeding and vaccines
* quick/effective but temporary

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9
Q

active immunity

A

resistance that occurs as a result of contact with the foreign body itself

ex) infection
* slow onset, but long term

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10
Q

3 steps of the immune response

A
  1. recognition
  2. elimination
  3. resolution
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11
Q

any foreign body is referred to as an

A

antigen (high molecular weight, usually a protein)

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12
Q

Haptens

A

act as antigens, but smaller molecular weight that binds to a large protein carrier

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13
Q

antigens are determined by their

A

major histocompatibility complex (MHC) - genetic cell marker (in humans located on 6th chromosome)

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14
Q

MHC determines

A

epitopes - surface antigens

  • located on cell surface
  • recognized as “foreign”
  • allows immune recognition
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15
Q

antigenic recognition: Dissemination (2 routes)

A
  1. lymphatic system

2. blood vascular system

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16
Q

lymphatic system process

A
  • antigen is taken to lymph nodes and sequestered
  • stimulate “naive” lymphocytes –> release cytokine called transfer factor (TF), –> effector lymphocytes produced –> sensitized memory lymphocytes produced, immune response initiated
17
Q

Phase 2 (elimination) 2 components

A
  1. cell mediated immunity response

2. humoral immunity response

18
Q

cell mediated response works from ___ and the humeral response works from ____

A

T-lymphocytes that are “thymic educated”

B-lymphocytes

19
Q

cell mediated response pathway

A

antigen reacts with the CD4 helper T lymphocytes, which are activated and release lymphokines. these activate CD8 (cytotoxic) lymphocytes, which become macrophages and release perforins, which cause the antigen to break down

20
Q

humeral mediated pathway

A

antigen reacts with B-lymph and CD4 helper T lymphocytes are activated and release lymphokines. B-lymph forms plasma cells, which produce antibodies, activated immune complement system (soluble mediator), terminates in formation of Membrane Attack Complex, which forms transmembrane channels

21
Q

immune complement system function - goal 1

A

forms membrane attack complex (MAC) - forms transmembrane channels that disrupts the cell membrane
lysis (destruction) of the foreign body

22
Q

immune complement system function - goal 2

A

opsonization of the antigen - complement fragments and antibodies coat the antigen; antigen phagocytized by macrophages

23
Q

order of anitbody formation

A
  • IgM, IgG, IgA
24
Q

antibodies

A

proteins produced by plasma cells to combat a specific foreign agent

25
the proteins are called
immunoglobulins
26
IgG
80% of antibodies in circulating fluids, most abundant
27
IgM
usually first immunoglobulin to be produced, may be an IgG precursor
28
IgA
attached to mucosal surfaces
29
IgE
attached to mast cells, mediates allergies, reaction to parasites *strongest immune reactions
30
IgD
- activates young B cells sequestered in the spleen | - usually used with IgM
31
L chains
- depend on amino acid sequence, but are not considered in classifying the antibody kappa - 65% lambda - 35%
32
Myelodysplastic syndrome
- bone marrow failure - not making platelets or WBCs - prone to infection and internal bleeding - pre leukemia
33
L chains may appear in the urine as
Bence Jones Protein (BJP) in multiple myeloma
34
myeloproliferative diseases
- too many plasma cells | - blood too sticky, too viscous
35
multiple myeloma
- malignant cancer of bone marrow - over production of plasma B cells, immunoglobulins - blood hyper viscosity (stains the heart) - sometimes characterized by acronym CRAB
36
CRAB
``` C = blood calcium (elevated) R = renal failure A = anemia B = bone lesions ```
37
Waldenstrom's macroglobulenemia
(same as multiple myeloma but no bone destruction) - B cells and IgM are overproduced - grows in lymph nodes - males 50+, may show monoclonal peak
38
Waldenstrom's macroglobulenemia treatment
- plasmapheresis | - progressive, 6.5 years survival