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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Edwards, W | - |
| dc.contributor.author | Sun, N | - |
| dc.contributor.author | Wang, Y | - |
| dc.contributor.author | Lu, Y | - |
| dc.contributor.author | Wang, C | - |
| dc.contributor.author | Mastronicola, D | - |
| dc.contributor.author | Scottà, C | - |
| dc.contributor.author | Romano, M | - |
| dc.contributor.author | Cejas, CM | - |
| dc.contributor.author | Espinet, A | - |
| dc.contributor.author | Lombardi, G | - |
| dc.contributor.author | Chiappini, C | - |
| dc.date.accessioned | 2026-03-08T10:27:38Z | - |
| dc.date.available | 2026-03-08T10:27:38Z | - |
| dc.date.issued | 2026-03-05 | - |
| dc.identifier | ORCiD: Cristiano Scottà https://orcid.org/0000-0003-3942-5201 | - |
| dc.identifier | ORCiD: Ciro Chiappini https://orcid.org/0000-0002-9893-4359 | - |
| dc.identifier.citation | Edwards, W. et al. (2026) 'Perfusion microbioreactor for CAR-Treg manufacturing', iScience, 115246, pp. 1–29. doi: 10.1016/j.isci.2026.115246. | en-GB |
| dc.identifier.uri | https://bura.brunel.ac.uk/handle/2438/32944 | - |
| dc.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. | en-GB |
| dc.description | 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. | - |
| dc.description | Supplemental Information is available online. | - |
| dc.description | This is a PDF of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability. This version will undergo additional copyediting, typesetting and review before it is published in its final form. As such, this version is no longer the Accepted Manuscript, but it is not yet the definitive Version of Record; we are providing this early version to give early visibility of the article. Please note that Elsevier’s sharing policy for the Published Journal Article applies to this version, see: https://www.elsevier.com/about/policies-andstandards/sharing#4-published-journal-article. Please also note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. | - |
| dc.description.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. | en-GB |
| dc.description.sponsorship | C.C. acknowledges funding from the European Union under the ERC Starting Grant ENBION 759577 and the medical research council under the Confidence in Concept award (MC_PC_18052); Medical Research Council (MRC); MFX (MicrofluidX) Ltd. acknowledges funding from the MRC DTP iCASE Studentship Scheme. | en-GB |
| dc.format.extent | 1–29 | - |
| dc.format.medium | Electronic | - |
| dc.language | en-GB | - |
| dc.language.iso | en | en-GB |
| dc.publisher | Elsevier | en-GB |
| dc.rights | https://creativecommons.org/licenses/by/4.0/ | - |
| dc.rights | Creative Commons Attribution 4.0 International | - |
| dc.title | Perfusion microbioreactor for CAR-Treg manufacturing | en-GB |
| dc.type | Article | en-GB |
| dc.date.dateAccepted | 2026-03-02 | - |
| dc.identifier.doi | https://doi.org/10.1016/j.isci.2026.115246 | - |
| dc.relation.isPartOf | iScience | - |
| pubs.publication-status | Published online | - |
| pubs.volume | 00 | - |
| dc.identifier.eissn | 2589-0042 | - |
| dc.rights.license | https://creativecommons.org/licenses/by/4.0/legalcode.en | - |
| dcterms.dateAccepted | 2026-03-02 | - |
| dc.rights.holder | The Author(s) | - |
| dc.contributor.orcid | Scottà, Cristiano [0000-0003-3942-5201] | - |
| dc.contributor.orcid | Chiappini, Ciro [0000-0002-9893-4359] | - |
| dc.identifier.number | 115246 | - |
| Appears in Collections: | Department of Biosciences Research Papers * | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| FullText.pdf | Copyright © 2026 The Author(s). Published by Elsevier Inc. This is an open access article under a Creative Commons license (https://creativecommons.org/licenses/by/4.0/). | 2.97 MB | Adobe PDF | View/Open |
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