Vermylen C, Cornu G
Department of Pediatric Hematology, Cliniques Universitaires St. Luc, Catholic University of Louvain, Brussels, Belgium.
Am J Pediatr Hematol Oncol. 1994 Feb;16(1):18-21.
In Belgium and France, 42 patients underwent bone marrow transplantation (BMT) for treatment of sickle cell disease.
The patients were young and symptomatic, but without chronic organ damage. Engraftment occurred in all patients and was sustained in 36. These 36 patients became free of symptoms and had a change in electrophoresis of their hemoglobin toward the donor's pattern.
In five patients, engraftment was followed by bone marrow rejection. Two of these five patients underwent a second transplant, one at 62 days and the other at 21 months after the first transplant, and they are both doing well. The other three patients had autologous recovery of their own bone marrow. One patient died 3 months after marrow transplant of complications of graft-versus-host disease (GVHD). All the other patients are alive, with follow-up ranging from 1 to 75 months.
Concerning the long-term side effects, six patients had chronic GVHD disease. So far, eight patients returned to Africa where they are continuing to do well.
在比利时和法国,42例患者接受了骨髓移植(BMT)以治疗镰状细胞病。
患者均为年轻人且有症状,但无慢性器官损害。所有患者均实现植入,36例患者的植入得以维持。这36例患者症状消失,血红蛋白电泳向供者模式转变。
5例患者植入后发生骨髓排斥。这5例患者中有2例接受了第二次移植,分别在第一次移植后62天和21个月进行,目前情况良好。另外3例患者自身骨髓实现自体恢复。1例患者在骨髓移植后3个月死于移植物抗宿主病(GVHD)并发症。所有其他患者均存活,随访时间为1至75个月。
关于长期副作用,6例患者患有慢性GVHD疾病。到目前为止,8例患者返回非洲,他们在那里情况仍然良好。