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儿童干细胞移植受者的腺病毒感染:免疫恢复延迟的幼儿风险增加。

Adenovirus infection in paediatric stem cell transplant recipients: increased risk in young children with a delayed immune recovery.

作者信息

van Tol M J D, Kroes A C M, Schinkel J, Dinkelaar W, Claas E C J, Jol-van der Zijde C M, Vossen J M

机构信息

The Department of Paediatrics, Section of Immunology, Haematology, Oncology, Bone Marrow Transplantation and Autoimmunity, Leiden University Medical Centre (LUMC), Leiden, The Netherlands.

出版信息

Bone Marrow Transplant. 2005 Jul;36(1):39-50. doi: 10.1038/sj.bmt.1705003.

Abstract

Adenovirus (HAdV) infections are a frequent cause of morbidity and mortality after allogeneic human stem cell transplantation (HSCT). We report a retrospective single-centre study on 328 consecutive paediatric recipients of an allogeneic HSCT. During the first 6 months after HSCT, HAdV infection occurred in 37 children (cumulative incidence 12%). The highest incidence was found in young children up to 5 years of age, transplanted after 1994, with >2 log T-cell depletion of a graft of another than an HLA-genotypically identical related donor (actuarial frequency at 6 months 84%). Persistence of HAdV and spreading of the virus over multiple sites showed a trend towards the development of HAdV disease or death, but did not reach significance. Recovery of immunity after HSCT, that is, serum concentrations of IgM and peripheral blood counts of T cells and subsets, was delayed in children with an HAdV infection compared with noninfected children. In seven out of seven patients with HAdV DNA in serum and decreasing lymphocyte counts, the infection had a fatal course. Manipulation of cellular immunity either by tapering of immunosuppression, infusion of donor lymphocytes or immunotherapy using HAdV-specific T cells should be considered in graft recipients at risk for a severe HAdV infection.

摘要

腺病毒(HAdV)感染是异基因人类干细胞移植(HSCT)后发病和死亡的常见原因。我们报告了一项对328例连续接受异基因HSCT的儿科受者的回顾性单中心研究。在HSCT后的前6个月,37名儿童发生了HAdV感染(累积发病率12%)。发病率最高的是1994年后接受移植的5岁以下幼儿,其移植的移植物T细胞耗竭>2 log,供者与受者HLA基因型不完全相同(6个月时的实际发病率为84%)。HAdV的持续存在和病毒在多个部位的传播显示出HAdV疾病发生或死亡的趋势,但未达到显著水平。与未感染儿童相比,发生HAdV感染的儿童HSCT后免疫恢复延迟,即血清IgM浓度以及T细胞及其亚群的外周血计数恢复延迟。在血清中有HAdV DNA且淋巴细胞计数下降的7例患者中,感染均呈致命病程。对于有严重HAdV感染风险的移植物受者,应考虑通过逐渐减少免疫抑制、输注供者淋巴细胞或使用HAdV特异性T细胞进行免疫治疗来调控细胞免疫。

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