Post-transplant lymphoproliferative disorders

被引:302
作者
Gottschalk, S [1 ]
Rooney, CM
Heslop, HE
机构
[1] Texas Childrens Hosp, Ctr Cell & Gene Therapy, Texas Childrens Canc Ctr, Dept Pediat,Methodist Hosp,Baylor Coll Med, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Ctr Cell & Gene Therapy, Texas Childrens Canc Ctr, Dept Med,Methodist Hosp,Baylor Coll Med, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Ctr Cell & Gene Therapy, Texas Childrens Canc Ctr, Dept Mol Virol & Microbiol,Methodist Hosp,Baylor, Houston, TX 77030 USA
来源
ANNUAL REVIEW OF MEDICINE | 2005年 / 56卷
关键词
lymphoma; Epstein-Bair virus; solid organ transplant; hematopoietic stem cell transplant; immunotherapy;
D O I
10.1146/annurev.med.56.082103.104727
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Post-transplant lymphoproliferative disorder (PTLD) is a life-threatening complication after hematopoietic stem cell or solid organ transplantation. The majority of PTLD is of B-cell origin and associated with Epstein-Barr virus (EBV). During the past decade progress has been made in better understanding the pathogenesis of PTLD, and early detection strategies, such as serial measurement of EBV-DNA load in peripheral blood samples, have assisted in the identification of high-risk patients. In addition, novel immunotherapies have been developed, including the use of monoclonal antibodies and adoptive transfer of EBV-specific T cells. Despite these advances, it remains a major challenge to define indications for preemptive therapies for PTLD and to integrate novel therapeutic approaches with conventional therapies.
引用
收藏
页码:29 / 44
页数:16
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