Kylie Crompton, David E Godler, Ling Ling, Ngaire Elwood, Francoise Mechinaud-Heloury, Trisha Soosay Raj, Kuang-Chih Hsiao, Jacqueline Fleming, Karin Tiedemann, Iona Novak, Michael Fahey, Xiaofang Wang, Katherine J Lee, Paul B Colditz, Priya Edwards, Dinah Reddihough
{"title":"Umbilical Cord Blood Cell Clearance Post-Infusion in Immune-Competent Children with Cerebral Palsy.","authors":"Kylie Crompton, David E Godler, Ling Ling, Ngaire Elwood, Francoise Mechinaud-Heloury, Trisha Soosay Raj, Kuang-Chih Hsiao, Jacqueline Fleming, Karin Tiedemann, Iona Novak, Michael Fahey, Xiaofang Wang, Katherine J Lee, Paul B Colditz, Priya Edwards, Dinah Reddihough","doi":"10.1159/000527612","DOIUrl":null,"url":null,"abstract":"<p><p>Umbilical cord blood cells have therapeutic potential for neurological disorders, through a paracrine mechanism of action. A greater understanding of the safety and immunological effects of allogeneic donor cord blood cells in the context of a healthy recipient immune system, such as in cerebral palsy, is needed. This study aimed to determine how quickly donor cord blood cells were cleared from the circulation in children with cerebral palsy who received a single intravenous infusion of 12/12 human leucocyte antigen (HLA)-matched sibling cord blood cells. Twelve participants with cerebral palsy aged 2-12 years received cord blood cell infusions as part of a phase I trial of umbilical blood infusion for cerebral palsy. Digital droplet PCR analysis of DNA copy number variants specific to donor and recipient was used to assess donor DNA clearance at five timepoints post-infusion, a surrogate measure of cell clearance. Donor cells were cleared by 3 months post-infusion in 11/12 participants. When detected, donor DNA was at a fraction of 0.01-0.31% of total DNA with no signs of graft-versus-host disease in any participant. The donor DNA clearance times provided by this study have important implications for understanding the safety of allogeneic cord blood cell infusion for cerebral palsy and translational tissue engineering or regenerative medicine research in other disorders.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1159/000527612","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/10/19 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
Umbilical cord blood cells have therapeutic potential for neurological disorders, through a paracrine mechanism of action. A greater understanding of the safety and immunological effects of allogeneic donor cord blood cells in the context of a healthy recipient immune system, such as in cerebral palsy, is needed. This study aimed to determine how quickly donor cord blood cells were cleared from the circulation in children with cerebral palsy who received a single intravenous infusion of 12/12 human leucocyte antigen (HLA)-matched sibling cord blood cells. Twelve participants with cerebral palsy aged 2-12 years received cord blood cell infusions as part of a phase I trial of umbilical blood infusion for cerebral palsy. Digital droplet PCR analysis of DNA copy number variants specific to donor and recipient was used to assess donor DNA clearance at five timepoints post-infusion, a surrogate measure of cell clearance. Donor cells were cleared by 3 months post-infusion in 11/12 participants. When detected, donor DNA was at a fraction of 0.01-0.31% of total DNA with no signs of graft-versus-host disease in any participant. The donor DNA clearance times provided by this study have important implications for understanding the safety of allogeneic cord blood cell infusion for cerebral palsy and translational tissue engineering or regenerative medicine research in other disorders.
脐带血细胞通过旁分泌作用机制,具有治疗神经系统疾病的潜力。我们需要进一步了解异体供体脐带血细胞在受体免疫系统健康的情况下(如脑瘫)的安全性和免疫学效应。本研究旨在确定脑瘫患儿在接受12/12人类白细胞抗原(HLA)匹配的同胞脐带血细胞单次静脉输注后,供体脐带血细胞从血液循环中清除的速度。作为脐带血输注治疗脑瘫 I 期试验的一部分,12 名 2-12 岁的脑瘫患者接受了脐带血细胞输注。对供体和受体特异的DNA拷贝数变异进行数字液滴PCR分析,以评估输注后五个时间点的供体DNA清除率,这是细胞清除率的替代指标。11/12 名参与者的供体细胞在输注后 3 个月清除。检测到的供体 DNA 占总 DNA 的 0.01%-0.31%,没有任何参与者出现移植物抗宿主疾病的迹象。这项研究提供的供体DNA清除时间对于了解异体脐带血细胞输注治疗脑瘫的安全性以及其他疾病的组织工程或再生医学转化研究具有重要意义。