3D Printing as a Strategy to Scale-Up Biohybrid Hydrogels for T Cell Manufacture

The emergence of cellular immunotherapy treatments is introducing more efficient strategies to combat cancer as well as autoimmune and infectious diseases. However, the cellular manufacturing procedures associated with these therapies remain costly and time-consuming, thus limiting their applicability. Recently, lymph-node-inspired PEG-heparin hydrogels have been demonstrated to improve primary human T cell culture at the laboratory scale. To go one step further in their clinical applicability, we assessed their scalability, which was successfully achieved by 3D printing. Thus, we were able to improve primary human T cell infiltration in the biohybrid PEG-heparin hydrogels, as well as increase nutrient, waste, and gas transport, resulting in higher primary human T cell proliferation rates while maintaining the phenotype. Thus, we moved one step further toward meeting the requirements needed to improve the manufacture of the cellular products used in cellular immunotherapies.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2024-09-17
DOI
https://doi.org/10.1021/acsami.4c06183
Citations
6
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
1.70

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3D Printing as a Strategy to Scale-Up Biohybrid Hydrogels for T Cell Manufacture

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ACS Applied Materials & Interfaces
CAR-T cell therapy research
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article

3D Printing as a Strategy to Scale-Up Biohybrid Hydrogels for T Cell Manufacture

Miguel A. Mateos‐Timoneda, Judith Guasch, Fabião Santos, Elisabeth Engel, Sergi Rey-Viñolas, Imma Ratera, Jaume Veciana, Eduardo Pérez del Río, Miquel Castellote‐Borrell, Francesca Merlina
article en
6 citations

Abstract

The emergence of cellular immunotherapy treatments is introducing more efficient strategies to combat cancer as well as autoimmune and infectious diseases. However, the cellular manufacturing procedures associated with these therapies remain costly and time-consuming, thus limiting their applicability. Recently, lymph-node-inspired PEG-heparin hydrogels have been demonstrated to improve primary human T cell culture at the laboratory scale. To go one step further in their clinical applicability, we assessed their scalability, which was successfully achieved by 3D printing. Thus, we were able to improve primary human T cell infiltration in the biohybrid PEG-heparin hydrogels, as well as increase nutrient, waste, and gas transport, resulting in higher primary human T cell proliferation rates while maintaining the phenotype. Thus, we moved one step further toward meeting the requirements needed to improve the manufacture of the cellular products used in cellular immunotherapies.

ACS Applied Materials & InterfacesVol. 16(38)
Universitat Internacional de Catalunya (ES), Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (ES), Institut de Ciència de Materials de Barcelona (ES), Institute for Bioengineering of Catalonia (ES), Universitat Politècnica de Catalunya (ES)
Ministerio de Ciencia, Innovación y Universidades, European Commission, Generalitat de Catalunya, Ministerio de Economía y Competitividad, Max-Planck-Gesellschaft, Ministerio de Ciencia e Innovación, Horizon 2020 Framework Programme, Instituto de Salud Carlos III, European Regional Development Fund, H2020 Marie Skłodowska-Curie Actions
Openalex Percentile: Top 13%
CAR-T cell therapy research
1.70
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