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通过粒细胞输注继以外周血干细胞移植成功治疗慢性肉芽肿病中的侵袭性曲霉病。

Successful treatment of invasive aspergillosis in chronic granulomatous disease by granulocyte transfusions followed by peripheral blood stem cell transplantation.

作者信息

Bielorai B, Toren A, Wolach B, Mandel M, Golan H, Neumann Y, Kaplinisky C, Weintraub M, Keller N, Amariglio N, Paswell J, Rechavi G

机构信息

Department of Pediatric Hematology/Oncology, Sheba Medical Center, Tel-Hashomer, Israel.

出版信息

Bone Marrow Transplant. 2000 Nov;26(9):1025-8. doi: 10.1038/sj.bmt.1702651.

DOI:10.1038/sj.bmt.1702651
PMID:11100285
Abstract

Chronic granulomatous disease (CGD) is a primary immunodeficiency disorder characterized by impaired microbial killing and susceptibility to bacterial and fungal infections. Cure of the disease can be achieved by stem cell transplantation when performed early in its course, and before severe infections have developed. Invasive aspergillosis constitutes a very high risk for transplantation. We report a 4-year-old boy with X-linked CGD who underwent successful HLA-identical peripheral blood stem cell (PBSC) transplantation during invasive pulmonary aspergillosis and osteomyelitis of the left fourth rib, which was unresponsive to antifungal treatment. During the 2 months prior to the transplant he received G-CSF-mobilized granulocyte transfusions (GTX) from unrelated donors three times a week in addition to the antifungal treatment. This resulted in clinical improvement in his respiratory status. He also received GTX during the aplastic period after the conditioning regimen, until he had engrafted. Post-transplant superoxide generation test revealed that neutrophil function was within normal range. One year post transplant the CT scan showed almost complete clearance of the pulmonary infiltrates and a marked improvement in the osteomyelitic process. Based on other reports and our own experience, GTX can serve as important treatment in patients with CGD who have failed conventional anti-fungal treatment and for whom stem cell transplantation is the only chance for cure.

摘要

慢性肉芽肿病(CGD)是一种原发性免疫缺陷疾病,其特征为微生物杀伤功能受损以及易患细菌和真菌感染。若在疾病病程早期且严重感染尚未发生之前进行干细胞移植,可实现疾病的治愈。侵袭性曲霉病对移植构成极高风险。我们报告了一名患有X连锁CGD的4岁男孩,他在患有侵袭性肺曲霉病和左侧第四肋骨骨髓炎且抗真菌治疗无效的情况下,成功接受了 HLA 匹配的外周血干细胞(PBSC)移植。在移植前的2个月里,除抗真菌治疗外,他每周还接受3次来自无关供体的G-CSF动员的粒细胞输注(GTX)。这使他的呼吸状况得到临床改善。在预处理方案后的再生障碍期,他也接受了GTX,直至植入成功。移植后超氧化物生成试验显示中性粒细胞功能在正常范围内。移植后1年,CT扫描显示肺部浸润几乎完全清除,骨髓炎进程明显改善。基于其他报告和我们自己的经验,GTX可作为CGD患者重要的治疗手段,这些患者常规抗真菌治疗失败,且干细胞移植是唯一的治愈机会。

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