Introduction to SOT Flashcards

1
Q

Is being an organ donor now opt in or out?

A

You now have to opt out of being an organ donor, this changed in May 2020.
Therefore you can receive organs from either a living or a dead donor

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1
Q

What are some of the types of organ transplants you can undergo?

A

Heart
Liver
Lung
Pancreas
Bowel
Kidney
SPK - simultaneous pancreas and kidney
Multi-viscreal

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2
Q

What are the two types of donors?

A

You can either receive an organ from somebody you know (directed) or from anyone (altruistic) via the organ transplant list

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3
Q

What are some of the exclusions for being an organ donor?

A

CJD (Creutzfeldt–Jakob disease)
Ebola
Active cancer
HIV - but you can between two HIV patients

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4
Q

What is the first process of organ transplant?

A

Assessment and identification of patients that are in the inclusion criteria for receiving a transplant.
Transplant is usually the last choice for example in patient with dialysis failure

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5
Q

How do patients become entered on the transplant list?

A

The patients have to undergo an assessment with the MDT including consultants, surgeons but also including the Pharmacist
The patient’s inclusion criteria is assessed in addition to identifying any exclusion criteria to determine whether they are put on the transplant list.

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6
Q

What are some of the exclusion criteria for receiving an organ donation?

A

For example a life expectancy less than 2 years and conditions that would qualify the patient as being ‘too sick for transplant’

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7
Q

What is a transplant match dependent upon?

A

Recipient blood group matching
HLA compatibility

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8
Q

What is the aim for transplant?

A

To increase the life expectancy and quality of life for the patient

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9
Q

What is the main barrier to successful transplant with the organ efficiency optimised?

A

The patient’s own immune system due to it perceiving the transplanted organ as a foreign substance with risk of acute and chronic rejection.
A degree of immunosuppression must be received which can slowly be reduced over time as tolerance builds.

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10
Q

What are the different types of grafts?

A

Xenografts
Autografts
Isografts
Allografts

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11
Q

Define xenografts.

A

A graft between different species which has the greatest immune response.

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12
Q

Define autografts.

A

One part of the body being transplanted to another, no rejection occurs. This includes a skin graft.

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13
Q

Define isografts.

A

When a graft is between genetically identical individuals (identical twins)

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14
Q

Define allografts.

A

Between members of the same species, varied response due to the type of organ transplanted and the type of organ.

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15
Q

What aspect of the immune system is responsible for rejection?

A

Human leukocyte antigens (HLA) which are genes in major histocompatibility complexes (MHC) that help code for proteins that differentiate between self and non-self and therefore are the cause of rejection.

16
Q

Where are the two major histocompatibility complexes expressed?

A

MHC-I is expressed on the cell surface of all nucleated cells
MHC-II on antigen presenting cells such as macrophages and B cells

17
Q

How many signals are required for T-cell activation?

A

3 signals are required for T-cell activation. When they are activation they undergo clonal expansion and differentiate to express further effector functionals.
This results injury and cell death to the transplanted organ.

18
Q

What is the first signalling pathway?

A

Interaction between the TCR binding to the antigen presenting on the MHC complex.

19
Q

What is the second signalling pathway?

A

Co-stimulatory receptor/ligand interaction between the T-cell and the antigen presenting cell.
This is usually CD28 and CD80 and 86 and/or CD40 and the ligand

20
Q

Which pathways are activated by the co-stimulatory pathway?

A

Calcium-calcineurin pathway
MAPK
Protein kinase C - nuclear factor kappa B activation

This is responsible for transcription factor activation, bringing about these T-cell functions

21
Q

What is the third signalling pathway?

A

These involves growth factors present for cell cycle progression
This involves activation of PI-3K pathway and mTOR

22
Q

How is the host response to the transplant controlled?

A

HLA compatibility - poor compatibility, risk of the rejection is higher. Close match is required to ensure graft is accepted for longer.
Immunosuppression

23
Q

What genes are MHC I encoded by?

A

HLA-A, HLA-B, HLA-C

24
Q

What genes are MHC II encoded by?

A

HLA-DP, DQ or DR

25
Q

What are the strongest determinants for HLA compatibility?

A

HLA-DR more so than A or B region
Would want this match to be as close as possible

26
Q

What are the benefits of HLA-compatibility?

A

Better graft function
Fewer episodes of rejection
Longer graft survival due to less damage to the transplanted organ
Reduced immunosuppression and potency
Decreased risk of sensitisation

Mismatch can be overcome by immunosuppression