Background. Few data exist on the physiological aspects of pig-to-primate r
enal xenotransplantation.
Methods. Use of organs transgenic for human decay accelerating factor has a
llowed assessment of the metabolic and hormonal functions of these xenograf
ts.
Results. Porcine renal xenografts largely maintain plasma electrolyte homeo
stasis. An increase in proteinuria was detected that may result from graft
injury. In contrast to allotransplantation a severe anaemia developed requi
ring recipient treatment with exogenous human erythropoietin.
Conclusions. Our experience provides qualified encouragement for the likely
physiological compatibility of pig and primate species, but identifies are
as where a xenograft may not match the performance of an allograft.