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MINI REVIEW article

Front. Bioeng. Biotechnol.

Sec. Cell and Gene Therapy

Volume 13 - 2025 | doi: 10.3389/fbioe.2025.1613836

This article is part of the Research TopicDesign Strategies and Equipment Requirements for Efficient Process Development and Robust Manufacturing of Cell TherapiesView all 11 articles

The Potential of Microfluidic Cell Analysis in CAR T Cell Therapy Manufacturing

Provisionally accepted
  • 1University College London, London, United Kingdom
  • 2Autolus Limited, London, England, United Kingdom

The final, formatted version of the article will be published soon.

Despite significant success in treating hematological cancers, Chimeric Antigen Receptor (CAR) T cell therapies must overcome several challenges to become accessible to a wide patient population. With the high cost of treatment stemming partly from the complexity of the manufacturing process, there is a need for radical innovation in the ways those therapies are made. A crucial aspect of the manufacturing process is quality control (QC), responsible for monitoring the quality of the drug product. The use of microfluidic technology, in which microchannels are designed and fabricated to achieve high control of liquids, can increase sensitivity, lower the Limit of Detection (LoD), and improve time-to-result of analytical assays. This review examines how recently developed microfluidic devices for T cell analysis fit the requirements of QC testing in CAR T cell manufacturing. A particular focus is on cell counting, cell phenotyping, and cytotoxicity assessments, where a range of microfluidic approaches have been taken to deliver reliable analytical assays. The review not only highlights current limitations of microfluidic devices that hinder their implementation in manufacturing, but also their potential to expand on current QC testing.

Keywords: cell therapy manufacturing, Microfluidics, Critical quality attributes, Quality control, CAR T cell therapy

Received: 17 Apr 2025; Accepted: 01 Sep 2025.

Copyright: © 2025 Nikoniuk, Lilova, Thomas and Szita. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Nicolas Szita, n.szita@ucl.ac.uk

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.