Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/32944
Title: Perfusion microbioreactor for CAR-Treg manufacturing
Authors: Edwards, W
Sun, N
Wang, Y
Lu, Y
Wang, C
Mastronicola, D
Scottà, C
Romano, M
Cejas, CM
Espinet, A
Lombardi, G
Chiappini, C
Issue Date: 5-Mar-2026
Publisher: Elsevier
Citation: Edwards, W. et al. (2026) 'Perfusion microbioreactor for CAR-Treg manufacturing', iScience, 115246, pp. 1–29. doi: 10.1016/j.isci.2026.115246.
Abstract: Summary: Manufacturing cell and gene therapies (CGTs) at scale presents challenges in cost, product consistency, and adaptability to personalised treatments. Traditional large-volume bioreactors are designed to support cell growth through controlled nutrient delivery and gas exchange, but are poorly suited to the decentralised, small-batch production required for personalised therapies like Chimeric Antigen Receptor (CAR) T-cells. To address this, we have developed the KCL-Microbioreactor (K-MBR), a closed microbioreactor platform based on microfluidic principles. Engineered in polydimethylsiloxane (PDMS), the K-MBR combines spatial confinement, semi-continuous perfusion, and integrated viral transduction in a compact footprint enabling efficient gene delivery and robust expansion of therapeutic cells. We demonstrate the platform’s utility by generating functional CAR-Tregs targeting HLA-A2, achieving a 92% increase in yield compared to conventional methods. The K-MBR offers a streamlined, solution for CGT manufacturing, with potential to reduce productions cost and enhance scalability across a broad range of cell therapies.
Description: Highlights: • Perfusion microbioreactor achieves Treg expansion comparable to gold standard G-Rex device. • Spatial confinement increases lentiviral transduction efficiency of primary, human cells. • Compact, low-volume platform reduces the physical footprint of cell manufacturing. • Device supports future automation and advances progress toward point-of-care production.
Data and code availability: All data reported in this paper will be shared by Ciro Chiappini upon request; this paper does not report original code. All datasets generated and analysed in this study, including raw flow cytometry files and source data, are available from the lead contact upon reasonable request.
Supplemental Information is available online.
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URI: https://bura.brunel.ac.uk/handle/2438/32944
DOI: https://doi.org/10.1016/j.isci.2026.115246
Other Identifiers: ORCiD: Cristiano Scottà https://orcid.org/0000-0003-3942-5201
ORCiD: Ciro Chiappini https://orcid.org/0000-0002-9893-4359
Appears in Collections:Department of Biosciences Research Papers *

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