淋巴增殖性病變
医学
移植后淋巴增生性疾病
免疫学
爱泼斯坦-巴尔病毒
造血干细胞移植
干细胞
单克隆
过继性细胞移植
移植
单克隆抗体
发病机制
病毒
免疫系统
抗体
T细胞
淋巴瘤
内科学
生物
遗传学
作者
Stephen Gottschalk,Cliona M. Rooney,Helen E. Heslop
标识
DOI:10.1146/annurev.med.56.082103.104727
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.
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