TY - JOUR
T1 - Impact of 3D cell culture hydrogels derived from basement membrane extracts or nanofibrillar cellulose on CAR-T cell activation
AU - Revilla, Sonia Aristin
AU - Cutilli, Alessandro
AU - Cambiaso, Eugenia
AU - Rockx-Brouwer, Dedeke
AU - Frederiks, Cynthia Lisanne
AU - Falandt, Marc
AU - Levato, Riccardo
AU - Kranenburg, Onno
AU - Lindemans, Caroline A.
AU - Coffer, Paul James
AU - Peperzak, Victor
AU - Mocholi, Enric
AU - Cuenca, Marta
N1 - © 2025 The Author(s).
PY - 2025/9/19
Y1 - 2025/9/19
N2 - Hydrogel-based 3D culture systems are increasingly used for preclinical evaluation of cell-based immunotherapies, including chimeric antigen receptor T (CAR-T) cells. However, hydrogel properties can influence T cell behavior, potentially affecting interpretation of immunotherapy studies. We assessed CD4+ T and CAR-T cell responses in two chemically undefined matrices—Matrigel and basement membrane extract (BME)— and in a synthetic nanofibrillar cellulose (NFC) hydrogel. Although NFC was mechanically stiffer, T cell activation and proliferation were higher in NFC than in Matrigel or BME. Murine CD4+ T cells acquired a regulatory phenotype in Matrigel and BME but not in NFC. Similarly, CAR-T cell function was reduced in Matrigel and BME but maintained in NFC. These findings underscore how matrix composition can shape T cell responses in 3D culture. NFC provides a chemically defined alternative that preserves T cell activity, supporting its use in more accurate preclinical testing of immunotherapies.
AB - Hydrogel-based 3D culture systems are increasingly used for preclinical evaluation of cell-based immunotherapies, including chimeric antigen receptor T (CAR-T) cells. However, hydrogel properties can influence T cell behavior, potentially affecting interpretation of immunotherapy studies. We assessed CD4+ T and CAR-T cell responses in two chemically undefined matrices—Matrigel and basement membrane extract (BME)— and in a synthetic nanofibrillar cellulose (NFC) hydrogel. Although NFC was mechanically stiffer, T cell activation and proliferation were higher in NFC than in Matrigel or BME. Murine CD4+ T cells acquired a regulatory phenotype in Matrigel and BME but not in NFC. Similarly, CAR-T cell function was reduced in Matrigel and BME but maintained in NFC. These findings underscore how matrix composition can shape T cell responses in 3D culture. NFC provides a chemically defined alternative that preserves T cell activity, supporting its use in more accurate preclinical testing of immunotherapies.
KW - Biological sciences
KW - Biomaterials
KW - Cell biology
KW - Immune response
KW - Materials science
UR - https://www.scopus.com/pages/publications/105012943449
UR - https://www.mendeley.com/catalogue/19118fd7-02ac-3b94-8ac7-7f5900d2a15e/
U2 - 10.1016/j.isci.2025.113234
DO - 10.1016/j.isci.2025.113234
M3 - Article
C2 - 40837221
AN - SCOPUS:105012943449
SN - 2589-0042
VL - 28
JO - iScience
JF - iScience
IS - 9
M1 - 113234
ER -