Joint lectures ♾️ Flashcards

1
Q

What is the definition of transplantation?

A

Transplantation is the transfer of cells, tissues or organs from one part of the body to another or from one individual to another.

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2
Q

What are the types of grafts?

A

Autograft
Isograft
Allograft
Xenografts

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3
Q

What is each of the following?

autograft
Isograft
Allograft
Xenograft

A

autograft: Graft between 2 sites within the same individual.

Isograft: Graft between 2 genetically identical individuals.

Allograft: Graft between 2 genetically dissimilar animals of the same species.

xenograft: Graft between 2 animals of different species.

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4
Q

what are the genes coding for histocompatibility Antigens divided into?

A
  • MHC where incompatibility leads to rapid rejection.

- Minor transplantation antigens: incompatibility leads to slow rejection.

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5
Q

What are the main complications of organ transplantation?

A

1) Problems with the preservation and reperfusion of the donor organ.
2) Technical/surgical complications.
3) Rejection.
4) Complications of immunosuppressive therapy.
5) Recurrence of the original disease for which transplantation was carried out

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6
Q

What are the types of rejection?

A

1) Hyperacute graft rejection
2) Acute rejection
3) Chronic (long term) rejection

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7
Q

When does hyperacute graft rejection take place?

A

Occurs few hours after transplantation.

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8
Q

What is the cause of hyperacute graft rejection?

A
  • It is due to preformed antibodies, either natural antibodies to blood type antigens or anti-MHC antibodies formed in response to blood transfusions or previous transplants, or developed during pregnancy to the baby’s paternal MHC antigens.
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9
Q

What are the effectors of hyperacute graft rejection and what is the result?

A
  • Antibodies react with antigens on vascular endothelial cells and activate complement inducing its pathway.
  • The resulting damage blocks blood vessels and damages the transplanted organ.
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10
Q

What is a Pathology of hyperacute rejection?

A

Grossly: The kidney rapidly becomes cyanotic, mottled, and flaccid.

Microscopically: Immunoglobulin and complement are deposited in the vessel wall, causing:
1- Endothelial injury and fibrin-platelet thrombi.
2- Neutrophils accumulate within arterioles, glomeruli,
andperitubular capillaries.
3- As these changes become diffuse and intense, the glomeruli undergo thrombotic occlusion of the capillaries, and fibrinoid necrosis occurs in arterial walls.

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11
Q

Where do much of our understanding of the pathological aspects Solid organ transplantation come from?

A

Much of our understanding of the pathologic aspects of solid-organ transplantation is based on studies of renal allografts due to that the kidneys were the first transplanted solid organ and transplanted more than any other organ.

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12
Q

When does acute rejection take place?

A
  • Occurs in few days, weeks or month following transplantation.
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13
Q

What are the characteristics of acute Rejection?

A
  • Cellular or humoral immune mechanisms may predominate.

- Cellular is the most commonly seen.

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14
Q

What causes acute rejection?

A

As grafts contain donor antigen presenting cells that travel to the draining lymph nodes of the recipient and activate recipient T cells.

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15
Q

What are the effectors in acute rejection?

A
  • primarily cytotoxic T lymphocytes.

- These cells migrate to all tissues including the graft causing tissue damage.

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16
Q

What controls acute rejection?

A

has been significantly controlled by immunosuppressive therapy.

17
Q

What is a Pathology of Acute cellular rejection?

A

Microscopically, there may be

1- Extensive interstitial inflammatory cell infiltration and edema as well as mild interstitial hemorrhage.

2- Glomerular and peritubular capillaries contain large numbers of inflammatory cells that may also invade the tubules, causing focal tubular necrosis.

3- In addition to causing tubular damage, CD8+ T cells may injure vascular endothelial cells, causing a so-called endothelitis.

  • The affected vessels have swollen endothelial cells.
18
Q

What is the Pathology of Acute humoral rejection (rejection vasculitis)?

A

This may take the form of:

1- Necrotizing vasculitis with endothelial cell necrosis, neutrophilic infiltration, complement, and fibrin, and thrombosis.

2- Such lesions are associated with extensive necrosis of the renal parenchyma.

19
Q

When does chronic rejection take place?

A

after months or years.

20
Q

What causes chronic rejection?

A
  • Due to uptake of graft antigens by recipient APC.
  • Then, peptides from both MHC and minor histocompatibility antigens are presented by recipient antigen presenting cells.
21
Q

What are the effectors in chronic rejection?

A

Th1 cells that activate macrophages to cause chronic inflammation that leads to tissue injury and scarring.

22
Q

What is the Pathology of chronic rejection?

A

Chronic rejection is dominated by:

1- Vascular changes, interstitial fibrosis, and tubular atrophy with loss of renal parenchyma.

 The vascular changes consist of dense, intimal fibrosis, principally in the cortical arteries.

2- These vascular lesions result in renal ischemia, manifested by glomerular loss, interstitial fibrosis and tubular atrophy, and shrinkage of the renal parenchyma.

3- The glomeruli may show scarring, with duplication of basement membranes; this appearance is sometimes called chronic transplant glomerulopathy.

4- Chronically rejecting kidneys usually have interstitial mononuclear cell infiltrates of plasma cells and numerous eosinophils.

23
Q

Where does graft versus host disease occur?

A

bone marrow transplantation

24
Q

What causes graft versus host disease?

A

 The host possesses histocompatibility antigens that the graft lacks (occur to both MHC and minor H antigens).

 The graft contains immunologically competent cells.

25
Q

What are the symptoms of GVHD?

A

include rashes, diarrhea, and pneumonitis.

26
Q

Mention the procedures done to enhance graft survival.

A

Donor selection
Recipient preparation
Immuno-suppression

27
Q

How are donors selected in graft transplantation?

A

 The most important in donor selection is the MHC identity with the recipient; an identical twin is the ideal donor.

 Grafts from an HLA-matched sibling have 95-100% chance of success.

 Organs from a two or one DR matched cadaver have been used also with some success.

 In every case, ABO compatibility is essential.

28
Q

How is the recipient prepared in transplantation?

A
  • Immune suppression increases the risk of infection so protect the recipient by isolation and prophylactic antibiotics.
29
Q

how does immunosuppression take place in transplantation?

A

 Anti-inflammatory agents: Corticosteroids.

 Cytotoxic drugs:

  • They block DNA synthesis and affect rapidly dividing cells.
  • Azathioprine and cyclophosphamide are the most commonly used.

 Others: Cyclosporin A and tacrolimus