Physiological aspects of pig-to-primate renal xenotransplantation

被引:62
作者
Soin, B
Smith, KG
Zaidi, A
Cozzi, E
Bradley, JR
Ostlie, DJ
Lockhart, A
White, DJ
Friend, PJ [1 ]
机构
[1] Univ Oxford, Nuffield Dept Surg, John Radcliffe Hosp, Oxford OX3 9DU, England
[2] Univ Cambridge, Dept Nephrol, Cambridge, England
[3] Addenbrookes Hosp, Cambridge, England
[4] Univ Wales, Dept Cardiothorac Surg, Cardiff CF1 3NS, S Glam, Wales
[5] Heath Hosp, Dept Cardiothorac Surg, Cardiff, S Glam, Wales
[6] Univ Cambridge, Addenbrookes Hosp, Dept Surg, Cambridge CB2 2QQ, England
[7] Imutran Ltd, Nova Pharmaceut AG Co, Cambridge, England
[8] Mayo Clin Scottsdale, Dept Surg, Scottsdale, AZ USA
关键词
allograft; xenograft; renal transplantation; zoonotic infection; cross-species transplant; immunosuppression therapy; organ donation; interspecies physiology;
D O I
10.1046/j.1523-1755.2001.00973.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Few data exist on the physiological aspects of pig-to-primate renal xenotransplantation. Methods. Use of organs transgenic for human decay accelerating factor has allowed assessment of the metabolic and hormonal functions of these xenografts. Results. Porcine renal xenografts largely maintain plasma electrolyte homeostasis. An increase in proteinuria was detected that may result from graft injury. In contrast to allotransplantation a severe anaemia developed requiring recipient treatment with exogenous human erythropoietin. Conclusions. Our experience provides qualified encouragement for the likely physiological compatibility of pig and primate species, but identifies areas where a xenograft may not match the performance of an allograft.
引用
收藏
页码:1592 / 1597
页数:6
相关论文
共 25 条
[1]  
BAINTNER K, 1989, ACTA VET HUNG, V37, P69
[2]  
BARNAS U, 1997, KIDNEY INT S63, V52, pS78
[3]   Aspartate 171 is the major primate-specific determinant of human growth hormone - Engineering porcine growth hormone to activate the human receptor [J].
Behncken, SN ;
Rowlinson, SW ;
Rowland, JE ;
ConwayCampbell, BL ;
Monks, TA ;
Waters, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (43) :27077-27083
[4]   FUNCTIONAL STRUCTURE OF GLOMERULAR-FILTRATION BARRIER AND PROXIMAL TUBULI IN DEVELOPING FETAL AND NEONATAL PIG KIDNEY [J].
BERGELIN, ISS ;
KARLSSON, BW .
ANATOMY AND EMBRYOLOGY, 1975, 148 (03) :223-234
[5]  
Boesken W H, 1975, Proc Eur Dial Transplant Assoc, V11, P333
[6]   DIRECT ANTIGBM ANTIBODY INDUCED ALTERATIONS IN GLOMERULAR PERMSELECTIVITY [J].
BOYCE, NW ;
HOLDSWORTH, SR .
KIDNEY INTERNATIONAL, 1986, 30 (05) :666-672
[7]   GLOMERULAR CHARGE ALTERATIONS IN HUMAN MINIMAL CHANGE NEPHROPATHY [J].
BRIDGES, CR ;
MYERS, BD ;
BRENNER, BM ;
DEEN, WM .
KIDNEY INTERNATIONAL, 1982, 22 (06) :677-684
[8]   COMPLEMENT-INDEPENDENT NEPHROTOXIC NEPHRITIS IN GUINEA-PIG [J].
COUSER, WG ;
STILMANT, MM ;
JERMANOVICH, NB .
KIDNEY INTERNATIONAL, 1977, 11 (03) :170-180
[9]  
Cozzi E, 2000, TRANSPLANTATION, V70, P15
[10]  
EVANS DB, 1990, BIOTECHNOL APPL BIOC, V12, P161