Lecture 14: Immunological Aspects of Renal System (Part 2) Flashcards

1
Q

What are autografts?

A

Grafts exchanged from one part of body to another part in the same individual

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2
Q

What are isograts?

A

Grafts exchanged b/t different individuals of identical genetic constitutions (e.g. identical twins)

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3
Q

What are allografts?

A

Grafts exchanged between nonidentical membrane of same species (e.g. human to human)

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4
Q

What are xenografts?

A

Grafts exchanged between members of different species (e.g. pig to human)

  • more susceptible to rapid attack
  • can insert human genes to donor animals to increase chance of successful transplant
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5
Q

Why should a transplant take place within 36 hours of the donor’s death?

A

Trauma to the donor tissues can have the higher potential to release DAMPs, leading to immediate tissue damage

  • Clotting cascade: generates fibrin, which is a chemoattractant for immune cells
  • Increases local vascular permeability for immune cells to accumulate
  • Bradykinin: increase vasodilation and vascular permeability

*All leads to hyperacute allograft rejection

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6
Q

is ABO compatibility necessary for kidney transplants?

A

Yes (w/o solid immunosuppression)

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7
Q

With what transplants is ABO compatibility non important?

A

Non-vascularized tissue:

  • corneal transplantation
  • heart valve transplantation
  • bone and tendon grafts
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8
Q

How do you perform the Microcytotoxicity Test for for Preformed Antibodies?

A

1) Recipient serum with antibodies added to donor cells
2) Complement added after washing
3) Dye Added
4) If existing antibodies already existed, they are present

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9
Q

Why is HLA matching important?

A

Prevents graft rejection

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10
Q

What are convenient sources of lymphocytes for HLA typing

A

Cadaver: spleen or lymph node

Peripheral blood

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11
Q

How do you test for Class I HLA compatibility?

A

1) In separate dishes, antibodies to a specific antigen are added to donor are recipient cells.
2) Complement is added after washing –> Macs form pores in cells
3) Dye is added
4) Accumulation of dye in both cells mean there is compatibility

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12
Q

What happens if there is no compatibility when testing for Class I HLA compatibility?

A

Only donor cells will develop pores due to MAC complex and have dye accumulated in cells

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13
Q

Why is class II HLA compatibility not too important?

A

Class II only present on antigen presenting cells

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14
Q

What is mixed lymphocyte response?

A

1) Donor cells undergo radiation and do not proliferate.
2) These donor cells are mixed with recipient cells and 3H-thymidine.
3) If there is compatibility, proliferation of recipient cells does not occur.

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15
Q

What is a host versus graft disease?

A

Recipient rejects donor tissue

  • adaptive immune response: very strong
  • High frequency of T cells
  • immune memory plays role
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16
Q

What is direct allorecognition?

A

Donor APC cells present to recipient T cells

-recipient recognizes unprocessed allogeneic MHC molecules on graft APCs

17
Q

What is indirect allorecognition?

A

Donor alloantigens recognized by recipient class II molecules after they are processed by recipient APC

18
Q

How does host versus graft response occur?

A

1) DAMPs activate endothelial cells
2) T cells eventually enter allograft
3) T cells release cytokines, activating greater immune response

19
Q

Humoral rejection of transplants utilize what effector mechanism?

A

Th2 cells

-releases cytokines IL-4, IL-5, IL-10

20
Q

Cellular rejection of transplants utilize what effector mechanism?

A

Th1 cells

-releases IL-1, IFN-γ

21
Q

Describe hyperacute rejection.

A

Onset: Immediate

Mechanism: Preformed antibodies in recipient immediately attacks donor tissue

Presentation: Normally in accidental ABO incompatibility

22
Q

What type of hypersensitivity are hyperacute rejections?

A

Type II

23
Q

Describe acute rejection.

A

Onset: Weeks to months

Mechanism: Donor DC cells migrate to lymph nodes, triggering immune response in recipient —> leads to T cell mediated process. Also activation of classical complement pathway.

Presentation: Inflammation and leukocyte infiltration of graft vessels

24
Q

Describe chronic rejection

A

Onset: Months to years

Mechanism: T-cell mediated process - foreign MHC similar to self MHC carrying antigen. Macrophages infiltrate tissue

Presentation: Intimal thickening and fibrosis of graft vessels

25
Q

What type of hypersensitivity are acute and chronic rejections?

A

Type IV

26
Q

What is a graft versus host disease?

A

Donor tissue rejects recipient

27
Q

How does graft versus host response occur?

A

Mostly occurs in immunocompromised patients

-donor cytotoxic T cells attack allo-antigens of host either by Fas-FasL or perforins

28
Q

Where do graft versus host response normally occur?

A

Small bowel
Lung
Liver

29
Q

What is an acute graft versus host response?

A

Epithelial cell death in skin, liver, or GI

  • rash
  • jaundice
  • diarrhea
  • GI hemorrhage
30
Q

What is an chronic graft versus host response?

A

Fibrosis and atrophy of affected organ

-dysfunction of affected organ

31
Q

What type of hypersensitivity is graft versus host response?

A

Type IV