Organ transplantation is considered to be one of the greatest
achievements in modern medicine during the last decades. Improvements in
tissue typing for the human leukocyte antigens (HLA) class II antigens,
organ preservation, surgery, and the use of immunosuppressive drugs
made organ transplantation the treatment of choice for patients with
end-stage organ failure.
The success of organ transplantation has led to a marked increase in the
number of transplantations. However, with only a limited number of
transplantable organs available from living donors, the demand for donor
organs has far exceeded the supply. To expand the organ donor pool, the
transplant community searched for alternatives e.g. through the use of
donors after cardiac death. Organs donated after cardiac death are
considered less than optimal. The extended time from the termination of
the circulation, to the actual moment of death, to organ recovery, and,
finally, to the initiation of perfusion with cold preservation solutions
results in the initiation of irreversible ischemia/reperfusion (I/R)
injury. On transplantation in the recipient, reperfusion of the graft
triggers apoptotic cell death, and promotes the activation of an
inflammatory response, resulting in profound injury of the graft. Hence,
I/R injury is considered a risk factor for the development of delayed
graft function, primary non-function, and acute rejection of the graft.
The treatment of I/R injury is still unsatisfactory. Therefore, new
therapeutic interventions to reduce or prevent I/R injury remain
warranted.
The studies in this thesis describe two novel treatments to ameliorate
I/R injury: genetic and nutritional preconditioning.
http://repub.eur.nl/res/pub/30631/111202_Verweij%2C%20Marielle%20-%20BEWERKT.pdf
http://repub.eur.nl/res/pub/30631/111202_Verweij%2C%20Marielle%20-%20BEWERKT.pdf
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