Intravenous gammaglobulin (IVIG): A novel approach to improve transplant rates and outcomes in highly HLA-sensitized patients

被引:112
作者
Jordan, SC [1 ]
Vo, AA
Peng, A
Toyoda, M
Tyan, D
机构
[1] Univ Calif Los Angeles, Sch Med, Cedars Sinai Med Ctr, Comprehens Transplant Ctr, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Sch Med, Cedars Sinai Med Ctr, Transplant Immunol Lab, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Sch Med, Cedars Sinai Med Ctr, Transplantat & Immunogenet Lab, Los Angeles, CA 90024 USA
关键词
antibody-mediated rejection; desensitization; HLA antibody; immune modulation; IVIG; kidney transplantation;
D O I
10.1111/j.1600-6143.2005.01214.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Intravenous immunoglobulin (IVIG) products are derived from pooled human plasma and have been used for the treatment of primary immunodeficiency disorders for more than 24 years. Shortly after their introduction, IVIG products were also found to be effective in the treatment of autoimmune and inflammatory disorders. Over the past 2 decades, the list of diseases where IVIG has a demonstrable beneficial effect has grown rapidly. These include Kawasaki disease, Guillain-Barre syndrome, myasthenia gravis, dermatomyositis and demyelinating polyneuropathy. Recently, we have described a beneficial effect on the reduction of anti-HLA antibodies with subsequent improvement in transplantation of highly HLA-sensitized patients as well as a potent anti-inflammatory effect that is beneficial in the treatment of antibody-mediated rejection (AMR). These advancements have enabled transplantation of patients previously considered untransplantable. These studies and relevant mechanism(s) of action will be discussed here.
引用
收藏
页码:459 / 466
页数:8
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