在 CAR-T 细胞疗法中冷冻保存初始白细胞前高细胞浓度的优势。

IF 2.4 3区 医学 Q2 HEMATOLOGY
Blood Transfusion Pub Date : 2024-05-01 Epub Date: 2023-09-06 DOI:10.2450/BloodTransfus.542
Diego Carbonell, Silvia Monsalvo, Eva Catalá, Ana Pérez-Corral, Carolina Villegas, Carmen Falero, Gloria Ruano, Monica Martinez, Mi Kwon, Cristina Muñoz-Martínez, José Luis Díez-Martín, Jorge Gayoso, Javier Anguita
{"title":"在 CAR-T 细胞疗法中冷冻保存初始白细胞前高细胞浓度的优势。","authors":"Diego Carbonell, Silvia Monsalvo, Eva Catalá, Ana Pérez-Corral, Carolina Villegas, Carmen Falero, Gloria Ruano, Monica Martinez, Mi Kwon, Cristina Muñoz-Martínez, José Luis Díez-Martín, Jorge Gayoso, Javier Anguita","doi":"10.2450/BloodTransfus.542","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Chimeric antigen receptor (CAR) T-cell therapy is increasingly used in patients affected by B-cell lymphoma and acute lymphoblastic leukemia. For logistical reasons, initial apheresis products may be cryopreserved for shipment to manufacturing centers. Due to the characteristics of these patients, cells are often collected in large volumes, meaning more bags must be cryopreserved. This requires increased storage, time and monetary costs. In this context, we aimed to evaluate a high cell concentration cryopreservation protocol by centrifugation to standardize the initial CAR-T manufacturing procedure.</p><p><strong>Materials and methods: </strong>Sixty-eight processes of leukapheresis of 57 patients affected by refractory/relapsed B cell lymphoma and 9 patients affected by acute lymphoblastic leukemia who were eligible for anti-CD19 CAR-T cell treatment performed between June 2019 and October 2022 were analyzed. Whole blood count, percentage and number of T cells were assessed on the apheresis final product. The apheresis product, which was alternatively stored overnight at 4°C, was centrifuged, adjusting the volume to approximately 40 mL. The product was immediately cryopreserved to achieve a final cell concentration of 50-200×10<sup>6</sup> cells/ml for cryopreservation.</p><p><strong>Results: </strong>Leukapheresis volume was reduced by almost fivefold (median: 185 to 40 mL), resulting in a higher product concentration in one bag. In addition, the number of non-target cells (monocytes, platelets and erythrocytes) was also reduced during the development of CAR-T cell therapy, thereby maintaining T lymphocyte levels and providing a purer starting material.</p><p><strong>Discussion: </strong>The advantages of the protocol include reducing economic costs, saving storage space, simplifying the manufacturing process, and facilitating shipping logistics. In conclusion, we present a validated, simple, and cost-effective cell enrichment processing protocol that provides high-quality cryopreserved products as starting material for the CAR-T cell manufacturing process.</p>","PeriodicalId":49260,"journal":{"name":"Blood Transfusion","volume":" ","pages":"239-245"},"PeriodicalIF":2.4000,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11073629/pdf/","citationCount":"0","resultStr":"{\"title\":\"Advantages of high cell concentration prior to cryopreservation of initial leukapheresis in CAR-T cell therapy.\",\"authors\":\"Diego Carbonell, Silvia Monsalvo, Eva Catalá, Ana Pérez-Corral, Carolina Villegas, Carmen Falero, Gloria Ruano, Monica Martinez, Mi Kwon, Cristina Muñoz-Martínez, José Luis Díez-Martín, Jorge Gayoso, Javier Anguita\",\"doi\":\"10.2450/BloodTransfus.542\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Chimeric antigen receptor (CAR) T-cell therapy is increasingly used in patients affected by B-cell lymphoma and acute lymphoblastic leukemia. For logistical reasons, initial apheresis products may be cryopreserved for shipment to manufacturing centers. Due to the characteristics of these patients, cells are often collected in large volumes, meaning more bags must be cryopreserved. This requires increased storage, time and monetary costs. In this context, we aimed to evaluate a high cell concentration cryopreservation protocol by centrifugation to standardize the initial CAR-T manufacturing procedure.</p><p><strong>Materials and methods: </strong>Sixty-eight processes of leukapheresis of 57 patients affected by refractory/relapsed B cell lymphoma and 9 patients affected by acute lymphoblastic leukemia who were eligible for anti-CD19 CAR-T cell treatment performed between June 2019 and October 2022 were analyzed. Whole blood count, percentage and number of T cells were assessed on the apheresis final product. The apheresis product, which was alternatively stored overnight at 4°C, was centrifuged, adjusting the volume to approximately 40 mL. The product was immediately cryopreserved to achieve a final cell concentration of 50-200×10<sup>6</sup> cells/ml for cryopreservation.</p><p><strong>Results: </strong>Leukapheresis volume was reduced by almost fivefold (median: 185 to 40 mL), resulting in a higher product concentration in one bag. In addition, the number of non-target cells (monocytes, platelets and erythrocytes) was also reduced during the development of CAR-T cell therapy, thereby maintaining T lymphocyte levels and providing a purer starting material.</p><p><strong>Discussion: </strong>The advantages of the protocol include reducing economic costs, saving storage space, simplifying the manufacturing process, and facilitating shipping logistics. In conclusion, we present a validated, simple, and cost-effective cell enrichment processing protocol that provides high-quality cryopreserved products as starting material for the CAR-T cell manufacturing process.</p>\",\"PeriodicalId\":49260,\"journal\":{\"name\":\"Blood Transfusion\",\"volume\":\" \",\"pages\":\"239-245\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11073629/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Blood Transfusion\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2450/BloodTransfus.542\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/9/6 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Blood Transfusion","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2450/BloodTransfus.542","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/9/6 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:嵌合抗原受体(CAR)T 细胞疗法越来越多地用于 B 细胞淋巴瘤和急性淋巴细胞白血病患者。由于物流原因,最初的血液净化产品可能需要低温保存,以便运往制造中心。由于这些患者的特点,细胞收集量往往很大,这意味着必须冷冻保存更多的细胞袋。这就需要增加存储、时间和金钱成本。在这种情况下,我们旨在评估一种通过离心的高浓度细胞冷冻保存方案,以规范最初的 CAR-T 生产程序:分析了2019年6月至2022年10月期间对57名难治性/复发性B细胞淋巴瘤患者和9名急性淋巴细胞白血病患者进行的68次白细胞分离过程,这些患者均符合抗CD19 CAR-T细胞治疗的条件。全血细胞计数、T细胞的百分比和数量都是通过血液净化最终产品进行评估的。离心后,将离心产物的体积调整到约 40 毫升,然后在 4°C 下保存过夜。产品立即进行冷冻保存,以达到 50-200×106 个细胞/毫升的最终细胞浓度:结果:白细胞分离体积减少了近五倍(中位数:从 185 毫升到 40 毫升),从而提高了一袋产品的浓度。此外,在 CAR T 细胞疗法的开发过程中,非靶细胞(单核细胞、血小板和红细胞)的数量也减少了,从而保持了 T 淋巴细胞的水平,并提供了更纯净的起始材料:该方案的优点包括降低经济成本、节省储存空间、简化生产流程和方便物流运输。总之,我们提出了一种经过验证、简单且经济高效的细胞富集处理方案,它能提供高质量的冷冻保存产品,作为 CAR-T 细胞制造工艺的起始材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advantages of high cell concentration prior to cryopreservation of initial leukapheresis in CAR-T cell therapy.

Background: Chimeric antigen receptor (CAR) T-cell therapy is increasingly used in patients affected by B-cell lymphoma and acute lymphoblastic leukemia. For logistical reasons, initial apheresis products may be cryopreserved for shipment to manufacturing centers. Due to the characteristics of these patients, cells are often collected in large volumes, meaning more bags must be cryopreserved. This requires increased storage, time and monetary costs. In this context, we aimed to evaluate a high cell concentration cryopreservation protocol by centrifugation to standardize the initial CAR-T manufacturing procedure.

Materials and methods: Sixty-eight processes of leukapheresis of 57 patients affected by refractory/relapsed B cell lymphoma and 9 patients affected by acute lymphoblastic leukemia who were eligible for anti-CD19 CAR-T cell treatment performed between June 2019 and October 2022 were analyzed. Whole blood count, percentage and number of T cells were assessed on the apheresis final product. The apheresis product, which was alternatively stored overnight at 4°C, was centrifuged, adjusting the volume to approximately 40 mL. The product was immediately cryopreserved to achieve a final cell concentration of 50-200×106 cells/ml for cryopreservation.

Results: Leukapheresis volume was reduced by almost fivefold (median: 185 to 40 mL), resulting in a higher product concentration in one bag. In addition, the number of non-target cells (monocytes, platelets and erythrocytes) was also reduced during the development of CAR-T cell therapy, thereby maintaining T lymphocyte levels and providing a purer starting material.

Discussion: The advantages of the protocol include reducing economic costs, saving storage space, simplifying the manufacturing process, and facilitating shipping logistics. In conclusion, we present a validated, simple, and cost-effective cell enrichment processing protocol that provides high-quality cryopreserved products as starting material for the CAR-T cell manufacturing process.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Blood Transfusion
Blood Transfusion HEMATOLOGY-
CiteScore
6.10
自引率
2.70%
发文量
91
审稿时长
2 months
期刊介绍: Blood Transfusion welcomes international submissions of Original Articles, Review Articles, Case Reports and Letters on all the fields related to Transfusion Medicine.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信