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间充质基质细胞在儿科造血细胞移植中的作用:一项综述和一项用蜕膜基质细胞治疗急性移植物抗宿主病患儿的初步研究。

Mesenchymal Stromal Cells in Pediatric Hematopoietic Cell Transplantation a Review and a Pilot Study in Children Treated With Decidua Stromal Cells for Acute Graft-versus-Host Disease.

机构信息

Translational Cell Therapy Research (TCR), Division of Pediatrics, Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden.

Division of Pediatrics, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

出版信息

Front Immunol. 2020 Oct 19;11:567210. doi: 10.3389/fimmu.2020.567210. eCollection 2020.

Abstract

Mesenchymal stromal cells (MSCs) are rare precursors in all organs of the body. MSCs have profound anti-inflammatory effects and reduce alloreactivity and . In pediatric allogeneic hematopoietic cell transplantation (HCT), MSCs have mainly been used to treat acute graft-versus-host disease (GVHD). MSCs are commercially available for this indication in Canada, Japan, and New Zeeland. More rare indications for MSCs in pediatric patients include graft failure and chronic GVHD. MSCs from bone marrow, adipose tissue, umbilical cord, Wharton's jelly, placenta tissue, and decidua have been used, but the optimal clinical stromal cell source has not been compared in clinical trials. More experimental clinical indications using MSCs, such as sepsis, acute respiratory distress syndrome, hemorrhages, pneumo-mediastinum, and neuroinflammation have primarily been explored in animal models or adult HCT patients. MSCs have almost no if any side-effects. In this pilot study we report the outcome of six children treated with decidua stromal cells (DSCs) for steroid refractory acute GVHD. At 6 months, complete response was seen in four patients and partial response in two patients. One child with high-risk ALL died from relapse and a boy with sickle cell disease died from a cerebral hemorrhage. Five-year survival was 67% and all survivors showed a Lansky score of 100%. To conclude, MSCs from various organs are well-tolerated and have shown an encouraging outcome for acute GVHD in pediatric patients.

摘要

间充质基质细胞(MSCs)是体内所有器官中罕见的前体细胞。MSCs 具有很强的抗炎作用,可以减少同种异体反应性和移植物抗宿主病(GVHD)。在儿科异基因造血细胞移植(HCT)中,MSCs 主要用于治疗急性移植物抗宿主病(GVHD)。在加拿大、日本和新西兰,MSCs 已可用于治疗这种疾病。儿科患者中 MSCs 的其他罕见适应证包括移植物衰竭和慢性 GVHD。已经使用了来自骨髓、脂肪组织、脐带、华通氏胶、胎盘组织和蜕膜的 MSCs,但在临床试验中尚未比较过最佳的临床基质细胞来源。更多使用 MSCs 的实验性临床适应证,如败血症、急性呼吸窘迫综合征、出血、气胸和神经炎症,主要在动物模型或成人 HCT 患者中进行了探索。MSCs 几乎没有副作用。在这项初步研究中,我们报告了 6 名接受蜕膜基质细胞(DSC)治疗类固醇难治性急性 GVHD 的儿童的结果。在 6 个月时,4 名患者出现完全缓解,2 名患者出现部分缓解。一名患有高危 ALL 的儿童因复发而死亡,一名患有镰状细胞病的男孩因脑出血而死亡。5 年生存率为 67%,所有幸存者的 Lansky 评分均为 100%。总之,来自不同器官的 MSCs 耐受性良好,并且在儿科患者的急性 GVHD 中显示出令人鼓舞的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70a1/7604265/198e4487e842/fimmu-11-567210-g0001.jpg

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