Disorders of immunity Flashcards

1
Q

B-lymphocytes deficiency

A

increased chance of Bacterial infection

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2
Q

T-lymphocyte deficiency

A

fungal & viral infections

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3
Q

primary deficiency disease =

A

1) Burton’s diease (male, B-cell system)
2) Thymic aplasia (diGeorge’s syndrome)
- -defective T-cell system
3) Combo immunodeficiency

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4
Q

secondary deficiencies =

A

1) stress = more glucocorticoids
2) latrogenic = result of treatment (too much advil)
3) senescent = age relates loss of immune

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5
Q

cross reaction =

A

when multiple antigens act with an antibody

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6
Q

hypersensitivities

A

type 1 = anaphylactic
type 2 = antibody depend hypersensitivity
type 3 = immune complex injury
type 4 = delayed hypersensitive

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7
Q

type 2 (antibody depend hypersensitivity)

A

1) complement mediated mech
2) antibody dependent cytotoxicity
- -low antibody
3) antireceptor antibodies
- -block cell membrane r/c (ex-graves mimic TSI)

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8
Q

type 3 (immune complex injury)

A

antigens & antibodies

  • -serum sickness
  • -acute glomerulonephritis
  • -systemic lupus erythematosus (SLE) *
  • -arthus reactions
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9
Q

type 4 (delayed hypersensitivity)

A

cell mediated = skin rashes, contact dermatitis, tuberculosis

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10
Q

HLA (human leukocyte antigens)

A

these are the “flags” that molecules use to signal
MHC = surface protein = major histocompatability antigens
–located on chromosome 6
MHC 1 = on nucleated cells & platelets
MCH 2 = antigen presenting cells (dendritic cells, macrophages, B-cells, active T-cells
MHC 3 = complement system NOT a HLA

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11
Q

HLA disease & associations

A
  • -ankylosing spondylitis = HLA-B27
  • -B8 = autoimmune disease
  • -D2/D3 = lupus
  • -D4 = rheumatoid arthritis
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12
Q

major autoimmune diseases

A

1) single cell disorders
- -graves, hashimotos, myasthenia
2) multisystemic disorders
- -systemic lupus erythematosus, rheumatoid arthritis, enthesopathies, scleroderma, sjogrens syndrome

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13
Q

systemic lupus erythematosus (SLE)

A
  • -chronic inflammation **SKIN, kidney, serosal membrane, joints, heart, CNS
  • -young women 90% are 15-35yrs
  • -Genetic = no actual “lupus” gene tho. & intrinsic factor
  • -proliferation of B cells = inactivated suppressor cells
  • -numerous antibodies (well duh if B cells are increased)

–antibuclear antibodies (ANA) =double-strand DNA & the “SMITH antigen” 1/3 pts have this*

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14
Q

environmental factors for lupus (SLE)

A

1) UV light
2) Drugs
3) psoralens = tanning, cosmetics (P for plastics)
4) Estrogen
5) viruses (which (+) B cell production)
6) parasites = hypersensitivity
7) stress

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15
Q

classic triad associated with lupus (SLE)

A

butterfly rash
joint pain
fever

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16
Q

causes of death due to SLE

A

1) immune deficiency
2) glomerular disease
3) CNS disturbances

17
Q

SCLERODERMA

A

excessive fibrosis!
–elevated Von Willebrand facter
CREST syndrome

18
Q

organ / tissue response of scleroderma

A
  • -skin = raynaud’s phenomenon
  • -aligmentary trac= rubbery hose
  • -muscles = more kinase = weak
  • -kidneys = onion skinning
  • -lungs = restrictive lung disease
19
Q

CREST =

A
Calcinosis
Raynaud's phenomenon
Esophageal dysfunction
Sclerodactyly
Telangiectasias (dilated vessels in skin)
20
Q

Mixed connective tissue disease =

A

combo of lupus, plymyositis, scleroderma

21
Q

fibromyalgia syndrome

A

morning stiffness, trigger points. often disabling

–young woman who dislike alcohol. LOL

22
Q

polymyositis

A

inflammatory disease that damages skeletal muscle

  • -butterfly rash,, heliotrope eyelids, purple bumps on knuckles
  • -affects proximal muscles of extremities (hips, shoulders, neck flexors)
  • *spares extra-ocular muscles