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慢性肉芽肿病中来自匹配无关供者的造血干细胞移植

Hematopoietic stem cell transplantation from matched unrelated donors in chronic granulomatous disease.

作者信息

Schuetz C, Hoenig M, Gatz S, Speth F, Benninghoff U, Schulz A, Debatin K M, Friedrich W

机构信息

Department of Paediatrics, University Hospital Ulm, Paediatrics Eythstrasse 24, 89075, Ulm, Germany.

出版信息

Immunol Res. 2009;44(1-3):35-41. doi: 10.1007/s12026-008-8068-3.

Abstract

We report on 12 patients with chronic granulomatous disease transplanted with hematopoietic stem cells from matched unrelated (n = 9) or matched sibling donors (n = 3). The most common infectious complication was pulmonary aspergillosis, which nine patients had previously developed. Only 5 of 12 individuals had normal lung function prior to transplantation. At a mean follow-up of 53 months 9 of the 12 patients are alive including 7 of 9 following matched unrelated donor (MUD) transplantation. One patient died from ARDS, another from systemic BK virus infection, the third from complications of chronic graft-versus-host disease. Seven of nine surviving patients have normal lung function now. HSCT from a MUD is an option worth considering when no matched family donor is available. Restricted lung function prior to HSCT does not appear to be a limiting factor for such treatment.

摘要

我们报告了12例接受造血干细胞移植的慢性肉芽肿病患者,供者为匹配的无关供者(n = 9)或匹配的同胞供者(n = 3)。最常见的感染并发症是肺曲霉病,9例患者此前已发生。12例患者中只有5例在移植前肺功能正常。平均随访53个月时,12例患者中有9例存活,其中9例接受匹配无关供者(MUD)移植的患者中有7例存活。1例患者死于急性呼吸窘迫综合征(ARDS),另1例死于全身性BK病毒感染,第3例死于慢性移植物抗宿主病的并发症。9例存活患者中有7例目前肺功能正常。当没有匹配的家族供者时,来自MUD的造血干细胞移植是一个值得考虑的选择。造血干细胞移植前有限的肺功能似乎不是这种治疗的限制因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c32a/7102039/1b230323f525/12026_2008_8068_Fig1_HTML.jpg

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