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干细胞移植后 Epstein-Barr 病毒再激活的前瞻性评估:与单克隆丙种球蛋白病的关系。

Prospective evaluation of epstein-barr virus reactivation after stem cell transplantation: association with monoclonal gammopathy.

机构信息

Institute of Haematology, Rome, Italy.

出版信息

J Clin Immunol. 2010 Nov;30(6):894-902. doi: 10.1007/s10875-010-9454-x. Epub 2010 Aug 25.

DOI:10.1007/s10875-010-9454-x
PMID:20737201
Abstract

Epstein-Barr Virus (EBV) reactivation and EBV-related post-transplant lymphoproliferative disease (PTLD) have emerged as a severe complication after stem cell transplantation (SCT). We prospectively evaluated 104 consecutive patients receiving SCT either autologous or allogeneic. Fifty-two patients (50%) presented EBV DNA-emia and five of them developed PTLD proven or probable. PTLD rate was 9.6% among patients with EBV DNA-emia. One patient developed PTLD without EBV DNA-emia (0.96%). Overall PTLD incidence was 5.7%. No PTLD developed after autologous SCT. EBV DNA-emia was significantly more frequent after allogeneic than autologous SCT (60.7% vs 17.4%, p = 0.0002). At EBV reactivation, serum protein electrophoresis and immunofixation were assessed. Global incidence of γ-peak after allogeneic SCT with EBV reactivation was 65.3% (32/49 patients) and monoclonal gammopathy (MG) was identified in 23/28 evaluable patients (82%). All patients with PTLD developed γ-peak and in five of them MG was identified. MG is consistently associated with EBV DNA-emia and may help identification of progression to PTLD after allogeneic SCT.

摘要

题目:移植后 EBV 病毒(EBV)再激活与 EBV 相关的淋巴增殖性疾病(PTLD)已成为干细胞移植(SCT)后的严重并发症。

方法:我们前瞻性评估了 104 例接受自体或同种异体 SCT 的连续患者。

结果:52 例(50%)患者出现 EBV DNA-emia,其中 5 例发生经证实或可能的 PTLD。

结论:PTLD 发生率在 EBV DNA-emia 患者中为 9.6%。1 例患者发生了无 EBV DNA-emia 的 PTLD(0.96%)。

结论:总体 PTLD 发生率为 5.7%。

结论:自体 SCT 后无 PTLD 发生。

结论:同种异体 SCT 后 EBV DNA-emia 明显比自体 SCT 更常见(60.7% vs 17.4%,p = 0.0002)。

结论:在 EBV 再激活时,评估血清蛋白电泳和免疫固定。

结论:同种异体 SCT 后 EBV 再激活时,γ-峰的总发生率为 65.3%(49 例患者中的 32 例),在 28 例可评估患者中,有 23 例(82%)发现单克隆丙种球蛋白病(MG)。

结论:所有发生 PTLD 的患者均出现 γ-峰,其中 5 例患者发现 MG。

结论:MG 与 EBV DNA-emia 一致,可能有助于识别同种异体 SCT 后进展为 PTLD。

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