Unit I - Immune System (Part 1) Flashcards

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
Q

the proteins are called

A

immunoglobulins

26
Q

IgG

A

80% of antibodies in circulating fluids, most abundant

27
Q

IgM

A

usually first immunoglobulin to be produced, may be an IgG precursor

28
Q

IgA

A

attached to mucosal surfaces

29
Q

IgE

A

attached to mast cells, mediates allergies, reaction to parasites
*strongest immune reactions

30
Q

IgD

A
  • activates young B cells sequestered in the spleen

- usually used with IgM

31
Q

L chains

A
  • depend on amino acid sequence, but are not considered in classifying the antibody

kappa - 65%
lambda - 35%

32
Q

Myelodysplastic syndrome

A
  • bone marrow failure
  • not making platelets or WBCs
  • prone to infection and internal bleeding
  • pre leukemia
33
Q

L chains may appear in the urine as

A

Bence Jones Protein (BJP) in multiple myeloma

34
Q

myeloproliferative diseases

A
  • too many plasma cells

- blood too sticky, too viscous

35
Q

multiple myeloma

A
  • malignant cancer of bone marrow
  • over production of plasma B cells, immunoglobulins
  • blood hyper viscosity (stains the heart)
  • sometimes characterized by acronym CRAB
36
Q

CRAB

A
C = blood calcium (elevated)
R = renal failure
A = anemia
B = bone lesions
37
Q

Waldenstrom’s macroglobulenemia

A

(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
Q

Waldenstrom’s macroglobulenemia treatment

A
  • plasmapheresis

- progressive, 6.5 years survival