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 applicabili...

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Detalles Bibliográficos
Autores: Pérez del Río, Eduardo|||0000-0003-2444-5621, Rey Viñoles, Sergi|||0000-0002-2128-7704, Santos, Fabião, Castellote-Borrell, Miquel, Merlina, Francesca, Veciana Miró, Jaume, Ratera Bastardas, Imma, Mateos Timoneda, Miguel Ángel|||0000-0001-7657-1414, Engel López, Elisabeth|||0000-0003-4855-8874, Guasch, Judith
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/416165
Acceso en línea:https://hdl.handle.net/2117/416165
https://dx.doi.org/10.1021/acsami.4c06183
Access Level:acceso abierto
Palabra clave:3D printing
3D hydrogels
T cells
Cell therapy
Cancer
Hydrogels
Layers scaffolds
Suspensions
Àrees temàtiques de la UPC::Enginyeria biomèdica::Biomaterials
Descripción
Sumario: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.