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首页> 外文期刊>Stem cells translational medicine. >Allogeneic Human Umbilical Cord Mesenchymal Stem Cells for the Treatment of Autism Spectrum Disorder in Children: Safety Profile and Effect on Cytokine Levels
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Allogeneic Human Umbilical Cord Mesenchymal Stem Cells for the Treatment of Autism Spectrum Disorder in Children: Safety Profile and Effect on Cytokine Levels

机译:同种异体人类脐带间充质干细胞治疗儿童自闭症谱系障碍:安全性概况和对细胞因子水平的影响

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Individuals with autism spectrum disorder (ASD) suffer from developmental disabilities that impact communication, behavior, and social interaction. Immune dysregulation and inflammation have been linked to children with ASD, the latter manifesting in serum levels of macrophage‐derived chemokine (MDC) and thymus, and activation‐regulated chemokine (TARC). Mesenchymal stem cells derived from umbilical cord tissue (UC‐MSCs) have immune‐modulatory and anti‐inflammatory properties, and have been safely used to treat a variety of conditions. This study investigated the safety and efficacy of UC‐MSCs administered to children diagnosed with ASD. Efficacy was evaluated with the Autism Treatment Evaluation Checklist (ATEC) and the Childhood Autism Rating Scale (CARS), and with measurements of MDC and TARC serum levels. Twenty subjects received a dose of 36 million intravenous UC‐MSCs every 12?weeks (four times over a 9‐month period), and were followed up at 3 and 12?months after treatment completion. Adverse events related to treatment were mild or moderate and short in duration. The CARS and ATEC scores of eight subjects decreased over the course of treatment, placing them in a lower ASD symptom category when compared with baseline. MDC and TARC inflammatory cytokine levels also decreased for five of these eight subjects. The mean MDC, TARC, ATEC, and CARS values attained their lowest levels 3 months after the last administration. UC‐MSC administration in children with ASD was therefore determined to be safe. Although some signals of efficacy were observed in a small group of children, possible links between inflammation levels and ASD symptoms should be further investigated.
机译:自闭症谱系障碍(ASD)的个体患有发育障碍,影响了沟通,行为和社会互动。免疫异常和炎症与ASD患儿有关,后者在巨噬细胞衍生的趋化因子(MDC)和胸腺的血清水平以及激活调节的趋化因子(TARC)中表现出来。源自脐带组织(UC-MSC)的间充质干细胞具有免疫调节和抗炎特性,已被安全地用于治疗多种疾病。这项研究调查了被诊断患有ASD的儿童服用UC‐MSC的安全性和有效性。通过自闭症治疗评估清单(ATEC)和儿童自闭症评定量表(CARS)以及MDC和TARC血清水平的测量来评估疗效。每十二周(二十个月内四次)对二十名受试者进行3600万静脉UC-MSC静脉注射,并在治疗完成后的第三个月和十二个月进行随访。与治疗有关的不良事件为轻度或中度,持续时间短。在治疗过程中,八名受试者的CARS和ATEC得分下降,与基线相比,他们的ASD症状类别更低。这八名受试者中有五名的MDC和TARC炎性细胞因子水平也降低了。上次给药后3个月,平均MDC,TARC,ATEC和CARS值达到最低水平。因此,确定在患有ASD的儿童中使用UC‐MSC是安全的。尽管在一小群儿童中观察到一些疗效信号,但应进一步研究炎症水平与ASD症状之间的可能联系。

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