医学
移植
干细胞
造血干细胞移植
间充质干细胞
再生障碍性贫血
造血
脐带血
再生障碍
胃肠病学
免疫学
外科
内科学
骨髓
病理
生物
遗传学
作者
Katarina Le Blanc,Håkan Samuelsson,Britt Gustafsson,Mats Remberger,Berit Sundberg,Johan Arvidson,Per Ljungman,Helena Lönnies,Silvia Nava,Olle Ringdén
出处
期刊:Leukemia
[Springer Nature]
日期:2007-05-31
卷期号:21 (8): 1733-1738
被引量:437
标识
DOI:10.1038/sj.leu.2404777
摘要
Seven patients underwent treatment with mesenchymal stem cells (MSCs), together with allogeneic hematopoietic stem cell transplantation (HSCT). MSCs were given to three patients for graft failure and four patients were included in a pilot study. HSCT donors were three human leukocyte antigen (HLA)-identical siblings, three unrelated donors and one cord blood unit. The conditioning was myeloablative in four patients and reduced in three patients. MSC donors were HLA-identical siblings in three cases and haploidentical in four cases. Neutrophil counts >0.5 × 109/l was reached at a median of 12 (range 10–28) days. Platelet counts >30 × 109/l was achieved at a median of 12 (8–36) days. Acute graft-versus-host disease (GVHD) grade 0–I was seen in five patients. Two patients developed grade II, which in one patient evolved into chronic GVHD. One severe combined immunodeficiency (SCID) patient died of aspergillosis, the others are alive and well. One patient, diagnosed with aplastic anemia had graft failure after her first transplantation and severe Henoch–Schönlein Purpura (HSP). After retransplantation of MSCs and HSCs, she recovered from both the HSP and aplasia. Thus, co-transplantation of MSC resulted in fast engraftment of absolute neutrophil count (ANC) and platelets and 100% donor chimerism, even in three patients regrafted for graft failure/rejection.
科研通智能强力驱动
Strongly Powered by AbleSci AI