Evaluation of a microfluidic chip-based cell sorter in clinical manufacturing processes to deplete or isolate CD4 regulatory T cells.

IF 2.5 3区 医学 Q2 HEMATOLOGY
Transfusion Pub Date : 2025-06-30 DOI:10.1111/trf.18324
Ruud Hulspas, M Felicia Ciuculescu, Carolina Sasso, Baochun Zhang, José A Cancelas, Jerome Ritz
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引用次数: 0

Abstract

Background: Clinical scale manufacturing for cell therapies requires reliable methods to purify specific cell types. Few microfluidic chip-based cell sorters have been integrated into manufacturing processes of therapeutic cells. Reports have highlighted the need to assess current requirements and explore areas for improvement.

Study design and methods: We evaluated Highway1, a new microfluidic chip-based cell sorter in the context of good manufacturing practice (GMP)-compliant manufacturing processes involving purification of CD4 T cell subsets. Tests explored throughput and processing time limits, as required in GMP-compliant purification of regulatory T cells (Tregs) and of CD4 T cells free of CD4 Tregs. Findings were used to establish conditions with the best balance between processing time and yield.

Results: Best average recovery (60%) was obtained when processed at 1-1.5 million cells/mL, purifying a target population of 33%. Weighing recovery against processing time, a sample concentration of 2.0 million cells/mL offers the optimum condition for sorting CD4 T cells free of CD4 Tregs from healthy blood. Similar tests also show that this device allows for shorter overall processing times to purify CD4 Tregs than previously reported for other microfluidic chip-based sorters, with the additional benefit of an essentially user intervention-free operation.

Discussion: The Highway1 allows for reliable selection of a highly pure subpopulation of CD4 T cells in a GMP-compliant, cell therapy manufacturing setting. As with conventional sorters, the purification process for Tregs still needs to be preceded by a pre-enrichment process to keep the total processing time within an acceptable range for clinical-grade cell manufacturing.

评估基于微流控芯片的细胞分选器在临床制造过程中消耗或分离CD4调节性T细胞。
背景:临床规模生产细胞疗法需要可靠的方法来纯化特定的细胞类型。很少有基于微流控芯片的细胞分选器被集成到治疗细胞的制造过程中。报告强调有必要评估目前的需求和探索需要改进的领域。研究设计和方法:我们评估了Highway1,一种新的基于微流控芯片的细胞分选器,该分选器符合良好生产规范(GMP),涉及CD4 T细胞亚群的纯化。试验探讨了符合gmp要求的调节性T细胞(Tregs)和不含CD4 Tregs的CD4 T细胞纯化的吞吐量和处理时间限制。研究结果用于确定加工时间和产量之间的最佳平衡条件。结果:在100 - 150万细胞/mL处理时,平均回收率为60%,纯化目标群体为33%。将回收率与处理时间进行权衡,样品浓度为200万个细胞/mL提供了从健康血液中分选不含CD4 Tregs的CD4 T细胞的最佳条件。类似的测试也表明,与之前报道的其他基于微流控芯片的分选器相比,该设备允许更短的总体处理时间来纯化CD4 treg,并且具有基本上无需用户干预操作的额外好处。讨论:Highway1允许在符合gmp的细胞治疗制造环境中可靠地选择高度纯的CD4 T细胞亚群。与传统的分选器一样,Tregs的纯化过程仍然需要在预处理过程之前进行,以使总处理时间保持在临床级细胞制造可接受的范围内。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Transfusion
Transfusion 医学-血液学
CiteScore
4.70
自引率
20.70%
发文量
426
审稿时长
1 months
期刊介绍: TRANSFUSION is the foremost publication in the world for new information regarding transfusion medicine. Written by and for members of AABB and other health-care workers, TRANSFUSION reports on the latest technical advances, discusses opposing viewpoints regarding controversial issues, and presents key conference proceedings. In addition to blood banking and transfusion medicine topics, TRANSFUSION presents submissions concerning patient blood management, tissue transplantation and hematopoietic, cellular, and gene therapies.
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