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供体淋巴细胞输注治疗异基因造血干细胞移植后爱泼斯坦-巴尔病毒相关淋巴增殖性疾病的疗效与安全性

[The efficacy and safety of donor lymphocyte infusion to treat Epstein-Barr virus associated lymphoproliferative diseases after allogeneic hematopoietic stem cell transplantation].

作者信息

Xu Lan-ping, Liu Dai-hong, Liu Kai-yan, Chen Huan, Han Wei, Wang Yu, Wang Jing, Shi Hong-xia, Huang Xiao-jun

机构信息

Institute of Hematology, People's Hospital, Beijing University, Beijing 100044, China.

出版信息

Zhonghua Nei Ke Za Zhi. 2010 Nov;49(11):955-8.

Abstract

OBJECTIVE

To analyse our series patients' data to assess its efficacy and safety of donor lymphocyte infusion (DLI) for Epstein-Barr virus (EBV) associated post-transplant lymphoproliferative disorders (PTLD) after allogeneic hematopoietic stem cell transplantation (HSCT).

METHODS

Patients received HSCT from November 2006 to November 2009 and diagnosed as EBV associated PTLD by pathological or clinical methods were enrolled in this study. Lymphocyte was prepared by COBE collector. Related haplo-donors were the alternative if the original donors was unavailable. A range of mononuclear cell (MNC) dose of (0.5 - 1.0) × 10(8)/kg was designed and the expected number of T lymphocyte included was at level of 10(7)/kg. Cyclosporine (CsA) trough concentration was kept in a therapeutic level.

RESULTS

Nine patients with PTLD received DLI 13 times, the median number of PBMC infused was 0.8 (0.16 - 1.03) × 10(8)/kg, CD(3)(+)T cell number was 4.2 (1.6 - 5.7) × 10(7)/kg. Seven patients received peripheral blood mononuclear cells (PBMC) from original haplo-identical donors, with 7 response and 6 complete remission. Defervescence occurred after 2 (1 - 5) d, and adenopathy began to recover in 6 (1 - 14) d after the initial infusion of leukocytes. Graft versus host diseases (GVHD) occurred in 6 recipients out of 7 evaluable patients, and all were controlled successfully. Three patients survived for 38, 23 and 3 months after PTLD.

CONCLUSION

In this small series cases, infusion of controlled dose of lymphocyte from primary donor is an effective and safe therapy for EBV associated PTLD after mismatched/haploidentical HSCT while the optimal regimen needs to be further studied.

摘要

目的

分析本系列患者的数据,以评估供体淋巴细胞输注(DLI)治疗异基因造血干细胞移植(HSCT)后与EB病毒(EBV)相关的移植后淋巴细胞增殖性疾病(PTLD)的疗效和安全性。

方法

选取2006年11月至2009年11月接受HSCT且经病理或临床方法诊断为EBV相关PTLD的患者纳入本研究。淋巴细胞通过COBE采集器制备。若原供体不可用,则选用相关单倍体供体。设计了一系列(0.5 - 1.0)×10⁸/kg的单个核细胞(MNC)剂量,预期包含的T淋巴细胞数量为10⁷/kg水平。环孢素(CsA)谷浓度维持在治疗水平。

结果

9例PTLD患者接受了13次DLI,输注的外周血单个核细胞(PBMC)中位数为0.8(0.16 - 1.03)×10⁸/kg,CD3⁺T细胞数量为4.2(1.6 - 5.7)×10⁷/kg。7例患者接受了来自原单倍体相同供体的外周血单个核细胞(PBMC),7例有反应,6例完全缓解。发热在初始输注白细胞后2(1 - 5)天消退,淋巴结病在6(1 - 14)天开始恢复。7例可评估患者中有6例发生移植物抗宿主病(GVHD),均成功得到控制。3例患者在PTLD后分别存活了38、23和3个月。

结论

在这个小系列病例中,输注来自主要供体的控制剂量淋巴细胞是治疗错配/单倍体相同HSCT后EBV相关PTLD的一种有效且安全的疗法,而最佳方案有待进一步研究。

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