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严重成骨不全症患者宫内移植后胎儿间充质干细胞在骨内的植入

Fetal mesenchymal stem-cell engraftment in bone after in utero transplantation in a patient with severe osteogenesis imperfecta.

作者信息

Le Blanc Katarina, Götherström Cecilia, Ringdén Olle, Hassan Moustapha, McMahon Robert, Horwitz Edwin, Anneren Göran, Axelsson Ove, Nunn Janice, Ewald Uwe, Nordén-Lindeberg Solveig, Jansson Monika, Dalton Ann, Aström Eva, Westgren Magnus

机构信息

Center for Allogeneic Stem Cell Transplantation, Karolinska Institutet, Karolinska University Hospital Huddinge, SE-141 86 Stockholm, Sweden.

出版信息

Transplantation. 2005 Jun 15;79(11):1607-14. doi: 10.1097/01.tp.0000159029.48678.93.

Abstract

BACKGROUND

Mesenchymal stem cells (MSC) are progenitors of mesenchymal tissues such as bone, cartilage, and adipose. Adult human leukocyte antigen (HLA)-matched MSC have been used in cellular therapies of bone disorders such as osteogenesis imperfecta, with promising results.

METHODS

A female fetus with multiple intrauterine fractures, diagnosed as severe osteogenesis imperfecta, underwent transplantation with allogeneic HLA-mismatched male fetal MSC in the 32nd week of gestation. Engraftment analyses of donor cells, immunologic reaction against donor cells, and the well-being of the patient were assessed.

RESULTS

At 9 months of age, on slides stained for osteocalcin or osteopontin, a centromeric XY-specific probe revealed 0.3% of XY-positive cells in a bone biopsy specimen. Whole Y genome fluorescent in situ hybridization staining showed a median of 7.4% Y-positive cells (range, 6.8%-16.6%). Bone histology showed regularly arranged and configurated bone trabeculae. Patient lymphocyte proliferation against donor MSC was not observed in co-culture experiments performed in vitro after MSC injection. Complementary bisphosphonate treatment was begun at 4 months. During the first 2 years of life, three fractures were noted. At 2 years of corrected age, psychomotor development was normal and growth followed the same channel, -5 SD.

CONCLUSIONS

The authors' findings show that allogeneic fetal MSC can engraft and differentiate into bone in a human fetus even when the recipient is immunocompetent and HLA-incompatible.

摘要

背景

间充质干细胞(MSC)是骨、软骨和脂肪等间充质组织的祖细胞。成人人类白细胞抗原(HLA)匹配的MSC已用于诸如成骨不全等骨疾病的细胞治疗,取得了有前景的结果。

方法

一名被诊断为严重成骨不全且有多处子宫内骨折的女性胎儿,在妊娠第32周接受了同种异体HLA不匹配的男性胎儿MSC移植。评估了供体细胞的植入分析、对供体细胞的免疫反应以及患者的健康状况。

结果

在9个月大时,在骨钙素或骨桥蛋白染色的载玻片上,着丝粒XY特异性探针显示骨活检标本中有0.3%的XY阳性细胞。全Y基因组荧光原位杂交染色显示Y阳性细胞的中位数为7.4%(范围为6.8%-16.6%)。骨组织学显示骨小梁排列规则且形态正常。在MSC注射后体外进行的共培养实验中未观察到患者淋巴细胞对供体MSC的增殖。在4个月时开始补充双膦酸盐治疗。在生命的头2年中,记录到3次骨折。在矫正年龄2岁时,精神运动发育正常,生长遵循相同的轨迹,低于平均标准差5。

结论

作者的研究结果表明,即使受体具有免疫活性且HLA不匹配,同种异体胎儿MSC也能在人类胎儿体内植入并分化为骨。

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