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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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
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spelling 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
rights_invalid_str_mv 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
dc.source.none.fl_str_mv reponame:UPCommons. Portal del coneixement obert de la UPC
instname:Universitat Politècnica de Catalunya (UPC)
instname_str Universitat Politècnica de Catalunya (UPC)
reponame_str UPCommons. Portal del coneixement obert de la UPC
collection UPCommons. Portal del coneixement obert de la UPC
repository.name.fl_str_mv
repository.mail.fl_str_mv
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