The Impact of Amotosalen Photochemical Pathogen Inactivation on Human Platelet Lysate

IF 2.1 4区 医学 Q4 CELL & TISSUE ENGINEERING Current stem cell research & therapy Pub Date : 2024-06-24 DOI:10.2174/011574888x307274240610113314
Willem Delabie, Dominique De Bleser, Vicky Vandewalle, Marie-Laurence De Prest, Philippe Vandekerckhove, Veerle Compernolle, Hendrik B. Feys
{"title":"The Impact of Amotosalen Photochemical Pathogen Inactivation on Human Platelet Lysate","authors":"Willem Delabie, Dominique De Bleser, Vicky Vandewalle, Marie-Laurence De Prest, Philippe Vandekerckhove, Veerle Compernolle, Hendrik B. Feys","doi":"10.2174/011574888x307274240610113314","DOIUrl":null,"url":null,"abstract":"Background: Human Platelet Lysate (hPL) is a platelet-derived and growth factor-rich supplement for cell culture. It can be prepared from surplus platelet concentrates initially intended for transfusion. Amotosalen-based photochemical pathogen inactivation of platelet concentrates is used in a number of blood establishments worldwide to minimize the risk of pathogen transmission from donor to patient. Method: This pathogen inactivation method has not been formally validated for direct use on hPL. Here, we have studied the impact of pathogen inactivation on hPL and compared it to untreated hPL prepared from pathogen-inactivated platelet concentrates or control hPL. We used mass spectrometry, ELISA, and in vitro mesenchymal stem cell culture for determining residual amotosalen, final growth factor content, and cell doubling, respectively. Result: The data have shown amotosalen concentrations to be reduced a thousand-fold following pathogen inactivation, leaving trace quantities of photosensitizer molecules in the final hPL product. Some growth factors have been reported to be significantly more impacted in hPL that is directly pathogen-inactivated compared to both control conditions. This has no significant effect on the growth kinetics of adipose-derived mesenchymal stem cells. Conclusion: We have concluded direct amotosalen-based pathogen inactivation to have a measurable impact on certain growth factors in hPL, but this does not outweigh the likely benefits of reducing the odds of donor-to-patient pathogen transmission.","PeriodicalId":10979,"journal":{"name":"Current stem cell research & therapy","volume":"44 1","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current stem cell research & therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/011574888x307274240610113314","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL & TISSUE ENGINEERING","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Human Platelet Lysate (hPL) is a platelet-derived and growth factor-rich supplement for cell culture. It can be prepared from surplus platelet concentrates initially intended for transfusion. Amotosalen-based photochemical pathogen inactivation of platelet concentrates is used in a number of blood establishments worldwide to minimize the risk of pathogen transmission from donor to patient. Method: This pathogen inactivation method has not been formally validated for direct use on hPL. Here, we have studied the impact of pathogen inactivation on hPL and compared it to untreated hPL prepared from pathogen-inactivated platelet concentrates or control hPL. We used mass spectrometry, ELISA, and in vitro mesenchymal stem cell culture for determining residual amotosalen, final growth factor content, and cell doubling, respectively. Result: The data have shown amotosalen concentrations to be reduced a thousand-fold following pathogen inactivation, leaving trace quantities of photosensitizer molecules in the final hPL product. Some growth factors have been reported to be significantly more impacted in hPL that is directly pathogen-inactivated compared to both control conditions. This has no significant effect on the growth kinetics of adipose-derived mesenchymal stem cells. Conclusion: We have concluded direct amotosalen-based pathogen inactivation to have a measurable impact on certain growth factors in hPL, but this does not outweigh the likely benefits of reducing the odds of donor-to-patient pathogen transmission.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
阿莫托沙林光化学病原体灭活对人体血小板裂解液的影响
背景:人血小板裂解液(hPL)是一种血小板衍生的、富含生长因子的细胞培养补充剂。它可以从最初用于输血的剩余血小板浓缩液中制备。全球许多血液机构都在使用基于阿莫托柳林的血小板浓缩物光化学病原体灭活技术,以最大限度地降低病原体从献血者传染给病人的风险。方法:这种病原体灭活方法尚未正式验证是否可直接用于 hPL。在此,我们研究了病原体灭活对 hPL 的影响,并将其与未经处理的病原体灭活血小板浓缩物制备的 hPL 或对照 hPL 进行了比较。我们使用质谱法、酶联免疫吸附法和体外间充质干细胞培养法分别测定了残留的阿莫托沙林、最终生长因子含量和细胞倍增。结果数据显示,在病原体失活后,阿莫托沙林的浓度降低了一千倍,最终的 hPL 产品中还残留着微量的光敏剂分子。据报道,与两种对照条件相比,病原体直接失活的 hPL 对某些生长因子的影响更大。这对脂肪间充质干细胞的生长动力学没有明显影响。结论我们得出结论,基于阿莫托品的直接病原体灭活对hPL中的某些生长因子有可测量的影响,但这并不能抵消降低捐献者向患者传播病原体几率可能带来的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Current stem cell research & therapy
Current stem cell research & therapy CELL & TISSUE ENGINEERING-CELL BIOLOGY
CiteScore
4.20
自引率
3.70%
发文量
197
审稿时长
>12 weeks
期刊介绍: Current Stem Cell Research & Therapy publishes high quality frontier reviews, drug clinical trial studies and guest edited issues on all aspects of basic research on stem cells and their uses in clinical therapy. The journal is essential reading for all researchers and clinicians involved in stem cells research.
期刊最新文献
Deciphering the Immunomodulatory Pathways of Mesenchymal Stem Cells Insights into Suture Stem Cells: Distributions, Characteristics, and Applications A Study on the Role of miR-126 in the Repair Process after Spinal Cord Injury Magnesium Regulates the Migration and Differentiation of NPMSCs via the Integrin Signaling Pathway Salvianolic Acid B Accelerates Osteoporotic Fracture Healing via LncRNA-MALAT1/miR-155-5p/HIF1A Axis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1