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...
| Autores: | , , , , , , , , , |
|---|---|
| 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 |
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3D printing as a strategy to scale-up biohybrid hydrogels for T cell manufacturePérez del Río, Eduardo|||0000-0003-2444-5621Rey Viñoles, Sergi|||0000-0002-2128-7704Santos, FabiãoCastellote-Borrell, MiquelMerlina, FrancescaVeciana Miró, JaumeRatera Bastardas, ImmaMateos Timoneda, Miguel Ángel|||0000-0001-7657-1414Engel López, Elisabeth|||0000-0003-4855-8874Guasch, Judith3D printing3D hydrogelsT cellsCell therapyCancerHydrogelsLayers scaffoldsSuspensionsÀrees temàtiques de la UPC::Enginyeria biomèdica::BiomaterialsThe 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.This research was funded by the Spanish Ministry of Science and Innovation (PID2020-115296RA-I00; PID2019-105622RB- I00; PID2021-128412OB-I00 European Union NextGeneratio- nEU/PRTR, and the “Ramó n y Cajal” program (RYC-2017- 22614)) as well as the Generalitat de Catalunya (SGRCat 2021- 00438; 2017-SGR-359; Tecnologies Emergents program of the General Directorate for Research − Nr. 001-P-001646, cofunded with FEDER Operational Program of Catalonia 2014−2020). The work was also supported by the Max Planck Society through the Max Planck Partner Group “Dynamic Biomimetics for Cancer Immunotherapy” in collaboration with the Max Planck Institute for Medical Research (Heidelberg, Germany). The authors are grateful for the financial support received from Instituto de Salud Carlos III through Consorcio Centro de Investigación Biomédica en Red (CIBER) with the project “Gels4ACT” (Nr. BBN20PIV02). This research was also supported by the European Union’s Horizon 2020 research and innovation program H2020-MSCA-COFUND-2016 (DOC- FAM, grant agreement Nr. 754397). The authors acknowledge financial support from the Spanish Ministry of Science and Innovation through the “Severo Ochoa” Program for Centres of Excellence in R&D (CEX2023-001263-S, CEX2019-000917-S and CEX2018-000789-S).Peer Reviewed20242024-01-0120242024-10-17journal articlehttp://purl.org/coar/resource_type/c_6501VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/2117/416165https://dx.doi.org/10.1021/acsami.4c06183reponame:UPCommons. Portal del coneixement obert de la UPCinstname:Universitat Politècnica de Catalunya (UPC)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2Attribution 4.0 Internationalhttp://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:upcommons.upc.edu:2117/4161652026-05-27T15:37:01Z |
| dc.title.none.fl_str_mv |
3D printing as a strategy to scale-up biohybrid hydrogels for T cell manufacture |
| title |
3D printing as a strategy to scale-up biohybrid hydrogels for T cell manufacture |
| spellingShingle |
3D printing as a strategy to scale-up biohybrid hydrogels for T cell manufacture Pérez del Río, Eduardo|||0000-0003-2444-5621 3D printing 3D hydrogels T cells Cell therapy Cancer Hydrogels Layers scaffolds Suspensions Àrees temàtiques de la UPC::Enginyeria biomèdica::Biomaterials |
| title_short |
3D printing as a strategy to scale-up biohybrid hydrogels for T cell manufacture |
| title_full |
3D printing as a strategy to scale-up biohybrid hydrogels for T cell manufacture |
| title_fullStr |
3D printing as a strategy to scale-up biohybrid hydrogels for T cell manufacture |
| title_full_unstemmed |
3D printing as a strategy to scale-up biohybrid hydrogels for T cell manufacture |
| title_sort |
3D printing as a strategy to scale-up biohybrid hydrogels for T cell manufacture |
| dc.creator.none.fl_str_mv |
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 |
| author |
Pérez del Río, Eduardo|||0000-0003-2444-5621 |
| author_facet |
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 |
| author_role |
author |
| author2 |
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 |
| author2_role |
author author author author author author author author author |
| dc.subject.none.fl_str_mv |
3D printing 3D hydrogels T cells Cell therapy Cancer Hydrogels Layers scaffolds Suspensions Àrees temàtiques de la UPC::Enginyeria biomèdica::Biomaterials |
| topic |
3D printing 3D hydrogels T cells Cell therapy Cancer Hydrogels Layers scaffolds Suspensions Àrees temàtiques de la UPC::Enginyeria biomèdica::Biomaterials |
| description |
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. |
| publishDate |
2024 |
| dc.date.none.fl_str_mv |
2024 2024-01-01 2024 2024-10-17 |
| dc.type.none.fl_str_mv |
journal article http://purl.org/coar/resource_type/c_6501 VoR http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2117/416165 https://dx.doi.org/10.1021/acsami.4c06183 |
| url |
https://hdl.handle.net/2117/416165 https://dx.doi.org/10.1021/acsami.4c06183 |
| dc.language.none.fl_str_mv |
Inglés eng |
| language_invalid_str_mv |
Inglés |
| language |
eng |
| dc.rights.none.fl_str_mv |
open access http://purl.org/coar/access_right/c_abf2 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ |
| dc.rights.openaire.fl_str_mv |
info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf |
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reponame:UPCommons. Portal del coneixement obert de la UPC instname:Universitat Politècnica de Catalunya (UPC) |
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UPCommons. Portal del coneixement obert de la UPC |
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