12: Renal Immunology Flashcards

1
Q

Risk factors for kidney injury

A

Age, race, genetic factors, HTN, DM, metabolic syndrome

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2
Q

What does AKI cause?

A

Metabolic acidosis and acute renal failure

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3
Q

Acute renal failure

A

Abrupt decrease in kidney function

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4
Q

How many critically ill patients have AKI?

A

Up to 30%

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5
Q

Early, middle, and late stage AKI: major players

A

Early: Th17, Th1
Middle: M1
Late: Th1

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6
Q

Role of Tregs in AKI

A

Prevent AKI progression and restrict inflammation, promote repair

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7
Q

Autografts, isograft, allografts and xenografts

A
  1. Autografts: from same individual
  2. Isografts: from an identical twin
  3. Allografts: from another human
  4. Xenografts: from another species
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8
Q

How to avoid rejection of a xenografts

A

Human HLA genes inserted into the genomes of donor animals

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9
Q

Microcytotoxicity test for pre-formed Abs steps

A
  1. Recipient serum with Abs added to donor cells
  2. Complement is added
  3. Dye is added
  4. If dye is detected in cells -> mismatch
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10
Q

Microcytotoxicity test for class I HLA compatibility

A
  1. Anti-HLA-A3 Abs are added to recipient cells + separately to donor cells
  2. Complement is added
  3. Dye is added
  4. If dye is found in recipient cell + in donor cell -> match!
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11
Q

Donor-host Ag disparities doesn’t matter in which tissues?

A

Cornea, heart valve, bone, tendon, and SCs

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12
Q

Mixed lymphocyte response for testing class II HLA compatibility

A
  1. Donor cells are irradiated so they cant proliferate
  2. Recipient cells are labeled with thymidine and added to donor cells
  3. If recipient T cells find Ags on donor DCs -> proliferate
  4. Cell proliferation noted by radioactive thymidine present in the cells -> no compatibility
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13
Q

Why are adaptive immune responses greater against grafts than they are against pathogens?

A

Higher frequency of T cells that recognize the graft as non self

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14
Q

Direct and indirect allorecognition **

A
  1. Direct: recipient T cells arrive in graft -> recognize MHC molecules on donor APCs
  2. Indirect: donor MHCs are taken up -> presented by recipient APCs for activation of recipient T cells
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