Abstract

The emergence of cell and gene therapies has generated significant interest in their clinical and commercial potential. However, these therapies are prohibitively expensive to manufacture and can require extensive time for development due to our limited process knowledge and understanding. The automated ambr250® stirred-tank bioreactor platform provides an effective platform for high-throughput process development. However, the original dual pitched-blade 20 mm impeller and baffles proved sub-optimal for cell therapy candidates that require suspension of microcarriers (e.g. for the culture of adherent human mesenchymal stem cells) or other particles such as activating Dynabeads® (e.g. for the culture of human T-cells). We demonstrate the development of a new ambr250® stirred-tank bioreactor vessel which has been designed specifically to improve the suspension of microcarriers/beads and thereby improve the culture of such cellular systems. The new design is unbaffled and has a single, larger elephant ear impeller. We undertook a range of engineering and physical characterizations to determine which vessel and impeller configuration would be most suitable for suspension based on the minimum agitation speed (NJS) and associated specific power input (P/V)JS. A vessel (diameter, T, = 60 mm) without baffles and incorporating a single elephant ear impeller (diameter 30 mm and 45° pitch-blade angle) was selected as it had the lowest (P/V)JS and therefore potentially, based on Kolmogorov concepts, was the most flexible system. These experimentally-based conclusions were further validated firstly with computational fluid dynamic (CFD) simulations and secondly experimental studies involving the culture of both T-cells with Dynabeads® and hMSCs on microcarriers. The new ambr250® stirred-tank bioreactor successfully supported the culture of both cell types, with the T-cell culture demonstrating significant improvements compared to the original ambr250® and the hMSC-microcarrier culture gave significantly higher yields compared with spinner flask cultures. The new ambr250® bioreactor vessel design is an effective process development tool for cell and gene therapy candidates and potentially for autologous manufacture too.

Highlights

  • Cell and gene therapies (CGTs), such as human mesenchymal stem cells and CAR-T cells (Wang and Riviere 2016), present a novel therapeutic modality to treat a range of chronic, age-related conditions and address current unmet clinical need

  • T-cell activation is critical to support the function of T-cells and involves an intra-cellular signalling cascade that results in proliferation, effector function, or death, depending on the intensity of the activation (Panagopoulou and Rafiq 2019)

  • The research undertaken in this study demonstrated the design and development of a new bioreactor vessel and impeller for the ambr250Ò high-throughput, automated bioreactor platform, resulting in improved cell production for microcarrier and bead-based cultures

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Summary

Introduction

Cell and gene therapies (CGTs), such as human mesenchymal stem cells (hMSCs; Silva Couto et al 2020) and CAR-T cells (Wang and Riviere 2016), present a novel therapeutic modality to treat a range of chronic, age-related conditions and address current unmet clinical need. Despite their clinical promise, currently approved CGTs suffer from a lack of scalable manufacture, high costs ([ $150,000 per dose), poorly defined manufacturing processes and a lack of effective small-scale models to support process development activity (Vormittag et al 2018). For hMSC and other allogeneic cell therapy applications, it will be important to establish larger-scale process development systems to validate findings established at the smaller scale

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