Sirolimus and mycophenolate mofetil for calcineurin-free immunosuppression in renal transplant recipients

被引:33
作者
Pescovitz, MD
Govani, M
机构
[1] Indiana Univ, Dept Surg, Indianapolis, IN 46202 USA
[2] Indiana Univ, Dept Immunol Microbiol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Dept Med, Indianapolis, IN 46202 USA
关键词
immunosuppressive therapy; mycophenolate mofetil (MMF); sirolimus; renal transplantation;
D O I
10.1053/ajkd.2001.27506
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
Calcineurin inhibitors, such as cyclosporine and tacrolimus, have been available for almost 20 years. Although these drugs are highly effective and represent the mainstay of transplant immunosuppression, they are associated with acute and chronic nephrotoxicity. Acute nephrotoxicity, which occurs in the early period after transplantation, leads to a higher rate of dialysis, and chronic nephrotoxicity may eventually result in graft loss. Acute and chronic nephrotoxicity Is becoming more common as the use of marginal kidneys for transplantation increases. Two recently available immunosuppressive agents, mycophenolate mofetil and sirolimus (rapamycin), have no nephrotoxicity. The use of these drugs in combination with other agents has led to the development of new paradigms of immunosuppressive therapy. This paper reviews the results of clinical trials that have investigated these new approaches to immunosuppression in renal transplant recipients. (C) 2001 by the National Kidney Foundation, Inc.
引用
收藏
页码:S16 / S21
页数:6
相关论文
共 9 条
[1]   Chronic cyclosporine nephropathy: The Achilles' heel of immunosuppressive therapy [J].
Bennett, WM ;
DeMattos, A ;
Meyer, MM ;
Andoh, T ;
Barry, JM .
KIDNEY INTERNATIONAL, 1996, 50 (04) :1089-1100
[2]   Sirolimus (rapamycin)-based therapy in human renal transplantation -: Similar efficacy and different toxicity compared with cyclosporine [J].
Groth, CG ;
Bäckman, L ;
Morales, JM ;
Calne, R ;
Kreis, H ;
Lang, P ;
Touraine, JL ;
Claesson, K ;
Campistol, JM ;
Durand, D ;
Wramner, L ;
Brattström, C ;
Charpentier, B .
TRANSPLANTATION, 1999, 67 (07) :1036-1042
[3]   Use of anti-CD25 monoclonal antibody in combination with rapamycin to eliminate cyclosporine treatment during the induction phase of immunosuppression [J].
Hong, JC ;
Kahan, BD .
TRANSPLANTATION, 1999, 68 (05) :701-704
[4]  
JARDINE AG, 2001, TRANSPL 2001 SAT S N
[5]   Immunosuppressive effects and safety of a sirolimus/cyclosporine combination regimen for renal transplantation [J].
Kahan, BD ;
Podbielski, J ;
Napoli, KL ;
Katz, SM ;
Meier-Kriesche, HU ;
Van Buren, CT .
TRANSPLANTATION, 1998, 66 (08) :1040-1046
[6]   Sirolimus in association with mycophenolate mofetil induction for the prevention of acute graft rejection in renal allograft recipients [J].
Kreis, H ;
Cisterne, JM ;
Land, W ;
Wramner, L ;
Squifflet, JP ;
Abramowicz, D ;
Campistol, JM ;
Morales, JM ;
Grinyo, JM ;
Mourad, G ;
Berthoux, FC ;
Brattström, C ;
Lebranchu, Y ;
Vialtel, P .
TRANSPLANTATION, 2000, 69 (07) :1252-1260
[7]   The immunosuppressive macrolide RAD inhibits growth of human Epstein-Barr virus-transformed B lymphocytes in vitro and in vivo:: A potential approach to prevention and treatment of posttransplant lymphoproliferative disorders [J].
Majewski, M ;
Korecka, M ;
Kossev, P ;
Li, SY ;
Goldman, J ;
Moore, J ;
Silberstein, LE ;
Nowell, PC ;
Schuler, W ;
Shaw, LM ;
Wasik, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) :4285-4290
[8]  
OSTRAAT O, 2000, 18 INT C TRANSPL SOC
[9]   Can antibody prophylaxis allow sparing of other immunosuppressives? [J].
Vincenti, F ;
Grinyo, J ;
Ramos, E ;
Nashan, B ;
Stuart, F ;
Kuypers, D ;
Brattstrom, C ;
Cho, S ;
Ekberg, H ;
Johnson, R .
TRANSPLANTATION PROCEEDINGS, 1999, 31 (1-2) :1246-1248