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使用人类白细胞抗原(HLA)匹配的同胞供者进行异基因造血干细胞移植后晚期巨细胞病毒感染的危险因素:供体淋巴细胞输注和早期巨细胞病毒感染既往史。

Risk factors for late cytomegalovirus infection after allogeneic stem cell transplantation using HLA-matched sibling donor: donor lymphocyte infusion and previous history of early CMV infection.

作者信息

Kim D H, Kim J G, Lee N Y, Sung W J, Sohn S K, Suh J S, Lee K S, Lee K B

机构信息

Department of Hematology/Oncology, Kyungpook National University Hospital, Daegu 700-721, Korea.

出版信息

Bone Marrow Transplant. 2004 Jul;34(1):21-7. doi: 10.1038/sj.bmt.1704528.

Abstract

An increased incidence of late cytomegalovirus (CMV) infection has been reported during the last decade since the introduction of ganciclovir (GCV) prophylaxis or GCV pre-emptive therapy. Given that a donor lymphocyte infusion (DLI) can induce more severe GVHD, this may predispose a patient to late CMV infection. In all, 64 patients (median age 36, M/F 38/26) underwent allogeneic stem cell transplantation (SCT) using a matched sibling donor with bone marrow (n=9) or peripheral blood stem cells (n=55). The overall incidence of CMV infection, early and late CMV infection was 46.9 (30/64), 42.2 (27/64), and 16.4% (9/55), respectively. Early CMV infection was treated with GCV pre-emptive therapy that produced a 92.6% success rate. Among the 20 patients who received 35 DLIs, late CMV infection developed in eight (42.1%) of 19 evaluable cases with a median onset at 127 days post transplant. Risk factors for late CMV infection in a logistic regression analysis included DLIs (P=0.001) and a previous history of CMV infection (P=0.006). In conclusion, late CMV infection was strongly associated with DLIs and a previous history of early CMV infection. Accordingly, extended surveillance of CMV antigenemia is recommended for patients receiving DLIs or who have a previous history of CMV infection.

摘要

自引入更昔洛韦(GCV)预防或GCV抢先治疗以来,在过去十年中已报告晚期巨细胞病毒(CMV)感染的发生率有所增加。鉴于供体淋巴细胞输注(DLI)可诱发更严重的移植物抗宿主病(GVHD),这可能使患者易发生晚期CMV感染。共有64例患者(中位年龄36岁,男/女为38/26)接受了同种异体干细胞移植(SCT),供体为匹配的同胞,采用骨髓(n = 9)或外周血干细胞(n = 55)。CMV感染、早期和晚期CMV感染的总发生率分别为46.9%(30/64)、42.2%(27/64)和16.4%(9/55)。早期CMV感染采用GCV抢先治疗,成功率为92.6%。在接受35次DLI的20例患者中,19例可评估病例中有8例(42.1%)发生了晚期CMV感染,中位发病时间为移植后127天。逻辑回归分析中晚期CMV感染的危险因素包括DLI(P = 0.001)和既往CMV感染史(P = 0.006)。总之,晚期CMV感染与DLI和既往早期CMV感染史密切相关。因此,建议对接受DLI或有既往CMV感染史的患者延长CMV抗原血症监测。

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