Preservation of Peripheral Blood Stem Cells (CD34+/CD38-) for Bone Marrow Transplantation in Thai Lymphoma Patients

S. Anuchapreeda, Banphot Shaengkhamnang, Pawaret Panyajai, S. Chiampanichayakul, Singkome Tima, P. Klangsinsirikul, P. Vongchan, A. Tantiworawit
{"title":"Preservation of Peripheral Blood Stem Cells (CD34+/CD38-) for Bone Marrow Transplantation in Thai Lymphoma Patients","authors":"S. Anuchapreeda, Banphot Shaengkhamnang, Pawaret Panyajai, S. Chiampanichayakul, Singkome Tima, P. Klangsinsirikul, P. Vongchan, A. Tantiworawit","doi":"10.12982/nlsc.2023.044","DOIUrl":null,"url":null,"abstract":"Abstract Hematopoietic stem cell transplantation (HSCT) is one method of lymphoma therapy. Peripheral blood stem cell (PBSC) separation, preservation, cell viability, and cell function before transplantation are important factors in the success rate of stem cell transplantation. This study aims to separate and estimate the efficiency of deep-freezing preservation in autologous PBSCs (CD34+/CD38-) from lymphoma patients undergoing stem cell transplantation. PBSCs were separated and collected by leukapheresis before being cryopreserved and stored in liquid nitrogen. The number of CD34+/CD45dim cells was investigated and compared with the subpopulation of CD34+/CD38- cells using conventional trypan blue exclusion method and 7-AAD before and after cryopreservation. Colony-forming units (CFUs) were determined to indirectly assess the viability and potency of the PBSCs. The result showed that CD34+/CD38– cells constituted 35.56% of total CD34+ cells and 0.05% of total nucleated cells (TNCs). After thawing, the number of CD34+/CD38- cells did not demonstrate significant differences compared with pre-storage. The percentage of CFU recovery was 94.74%. In this study, the storage process of deep-freezing cryopreservation demonstrated high-quality recovery of CD34+/CD38- cells from PBSCs for autologous hematopoietic stem cell transplantation in lymphoma patients. This result showed novel data about the preservation of CD34+/CD38- cells. Keywords: Lymphoma, Autologous peripheral blood stem cell, Blood cryopreservation, Bone marrow transplantation","PeriodicalId":132692,"journal":{"name":"Natural and Life Sciences Communications","volume":"21 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural and Life Sciences Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12982/nlsc.2023.044","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Abstract Hematopoietic stem cell transplantation (HSCT) is one method of lymphoma therapy. Peripheral blood stem cell (PBSC) separation, preservation, cell viability, and cell function before transplantation are important factors in the success rate of stem cell transplantation. This study aims to separate and estimate the efficiency of deep-freezing preservation in autologous PBSCs (CD34+/CD38-) from lymphoma patients undergoing stem cell transplantation. PBSCs were separated and collected by leukapheresis before being cryopreserved and stored in liquid nitrogen. The number of CD34+/CD45dim cells was investigated and compared with the subpopulation of CD34+/CD38- cells using conventional trypan blue exclusion method and 7-AAD before and after cryopreservation. Colony-forming units (CFUs) were determined to indirectly assess the viability and potency of the PBSCs. The result showed that CD34+/CD38– cells constituted 35.56% of total CD34+ cells and 0.05% of total nucleated cells (TNCs). After thawing, the number of CD34+/CD38- cells did not demonstrate significant differences compared with pre-storage. The percentage of CFU recovery was 94.74%. In this study, the storage process of deep-freezing cryopreservation demonstrated high-quality recovery of CD34+/CD38- cells from PBSCs for autologous hematopoietic stem cell transplantation in lymphoma patients. This result showed novel data about the preservation of CD34+/CD38- cells. Keywords: Lymphoma, Autologous peripheral blood stem cell, Blood cryopreservation, Bone marrow transplantation
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
外周血干细胞(CD34+/CD38-)在泰国淋巴瘤患者骨髓移植中的保存
摘要造血干细胞移植(HSCT)是淋巴瘤的治疗方法之一。外周血干细胞(Peripheral blood stem cell, PBSC)在移植前的分离、保存、细胞活力和细胞功能是影响干细胞移植成功率的重要因素。本研究旨在分离和评估干细胞移植淋巴瘤患者自体PBSCs (CD34+/CD38-)的深度冷冻保存效率。PBSCs经白细胞分离收集,冷冻保存于液氮中保存。采用常规台锥蓝排除法和7-AAD检测冷冻前后CD34+/CD45dim细胞数量,并与CD34+/CD38-细胞亚群进行比较。测定菌落形成单位(cfu),间接评估PBSCs的活力和效力。结果表明,CD34+/CD38 -细胞占总CD34+细胞的35.56%,占总有核细胞(TNCs)的0.05%。解冻后,CD34+/CD38-细胞数量与保存前无显著差异。CFU回收率为94.74%。在本研究中,深度冷冻保存的储存过程表明,PBSCs高质量地恢复CD34+/CD38-细胞用于淋巴瘤患者的自体造血干细胞移植。这一结果为CD34+/CD38-细胞的保存提供了新的数据。关键词:淋巴瘤,自体外周血干细胞,血液冷冻保存,骨髓移植
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
CiteScore
0.20
自引率
0.00%
发文量
0
期刊最新文献
Population Structure and Functional Diversity of Rice Landraces: A Review Terminalia bellirica Extract Suppresses SARS-Cov-2 Nucleocapsid-Induced Inflammation in A549 Cells Skeletal Growth Status Agreement in a Group of Thai Children and Adolescents: A Comparative Analysis of Fishman's Skeletal Maturation and Baccetti's Cervical Vertebral Maturation Indices Optimization of Rice Flour, Corn Starch and Modified Tapioca Starch to Produce Gluten Free Cookies Potential use of Polyphenol-Enriched Extract from Moringa oleifera Leaves as an Active Ingredient in Sunscreen
×
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