Immuno deficiency 2 Flashcards

1
Q

symptoms of di george syndrome

A
  • lack of development of the media stinum
  • cadiac anomalies
  • hypoplastic thymus or complete absence of the thymus
  • hypocalcemia (resulting from parathyroid hypoplasia
  • facial abnormalities eg cleft palate
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2
Q

cause of di george

A

-deletion of chromosome 22

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3
Q

mnemonic for di george syndrome

A

CATCH 22

  • cardiac anomalies
  • abnormal face
  • thymic aplasia
  • cleft palate
  • hypocalcemia
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4
Q

immunological symptoms of di george

A
  • recurrent infection with
  • intracellular bacteria
  • fungi
  • large viruses
  • also pyogenic organisms due to B cell activation by t cells
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5
Q

SCID

A
  • sever combined immune deficiency
  • numerous forms of SCID that can result from any one of several genetic defects
  • both humoral and cell mediated immunity are compromised due to the loss of b cell activation by t cells
  • patients are susceptible to all types of infections
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6
Q

what is the most common form of scid, what causes it?

A
  • mutation of the common chain of the IL2 receptor
  • this is called x linked severe combines immunodeficiency
  • IL2 is still made and functional but it can not bind to the mutated receptor to cause any effect
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7
Q

other forms of scid, other than x linked

-two types that are the most important and then the others are essentially mutations that would cause scid

A
  • ADA def (adenosine deaminase)
  • bare lymphocyte syndrome: your cels either dont have hla class 1 or 2
  • abnormal signal transduction (mutations of protein kinase JAK3 or ZAP70) (RAG1 and RAG2)
  • mutations of the CD3 molecule
  • defective cytokine production
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8
Q

treatment of scid

A
  • reconstitution of the immune system with stem cell transplant
  • BUT beware of GVH disease
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9
Q

wiskott aldridge syndrome

-symptoms and teatment

A
  • immunodef
  • thrombocytopenia (purpura)
  • eczema
  • stem cell transplant
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10
Q

ataxia telangiectasis

A

ataxia

-telangiectasia

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11
Q

secondary immunodeficinecy of the humoral system

A
  • lymphoma
  • myeloma
  • burns (lose antibodies rapidly through the plasma being secreted at the site)
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12
Q

secondary immunodefs of cell mediated immunity

A

-patients taking immunosupresents
-malnutrition
-
viral infections especially HIv
-aging

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13
Q

what does hiv make contact with in order to effect the host

A
  • gp120 on CD4 protein

- gp41 on CCR5 (chemokine receptor)

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14
Q

what are the steps following an untreated hiv infection

A
  • viral load spikes, t cells diminish progressively for 6/7 weeks until it begins to taper off
  • viral load goes back down to nearly nothing by 12 weeks
  • t cells go back up a but and then this stays constant for years until the virus suddenly becomes active and replicated very quickly until the host loses all of their t cells and begins to get opportunistic infections
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15
Q

laboratory diagnosis of HIV

A
  • can detect HIV antigen or antibody in the blood
  • reversal of the normal 2:1 ratio of Cd4 to CD8
  • measure serum levels of HIV RNa to follow progress of the disease
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16
Q

what is the most common immunodeficiency

A
  • aging
  • significant and continuous deficiency
  • decreasing number and function of many cell types such as neutrophils, APC’s, NK cells, and t cells