Induction Immunosuppressive Therapy in Kidney Transplantation

被引:11
作者
Bakr, Mohamed Adel [1 ]
Nagib, Ayman Maher [1 ]
Donia, Ahmed Farouk [1 ]
机构
[1] Mansoura Univ, Urol Nephrol Ctr, Mansoura, Egypt
关键词
End-stage renal disease; Antithymocyte globulin; Rituximab; Interleukin; 2; receptor; Acute rejection; Delayed graft function; RABBIT ANTITHYMOCYTE GLOBULIN; HIGHLY SENSITIZED PATIENTS; DELAYED GRAFT FUNCTION; PEDIATRIC RENAL-TRANSPLANTATION; CONTAINING TRIPLE THERAPY; LOW-DOSE CYCLOSPORINE; POSITIVE CROSS-MATCH; ANTI-HLA ANTIBODIES; BASILIXIMAB INDUCTION; HEPATITIS-C;
D O I
10.6002/ect.25Liver.L58
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Induction therapy after kidney transplantation is intensive immunosuppression in the initial days after transplant when the immune system of the recipient has the first contact with donor antigens. Initial intensive immunosuppression may be required to prevent acute rejection and graft loss, and subsequent immuno-suppression may be decreased to minimize adverse events associated with immunosuppressive drugs. Induction agents include lymphocyte-depleting antibodies such as rabbit antithymocyte globulin, alemtuzumab, muromonab-CD3, rituximab, and bortezomib; lymphocyte-nondepleting antibodies such as interleukin 2 receptor antibodies; and other discontinued or investigational agents such as efalizumab and alefacept. Induction therapy may be adjusted for special situations such as living-donor kidney transplant, pediatric transplant, hepatitis C virus-seropositive recipients, recipients who require desensitization, patients who are at risk for developing delayed graft function, and old donors. The optimal immunosuppressive regimen may vary, and clinical practice guidelines are available.
引用
收藏
页码:60 / 69
页数:10
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