TY - JOUR
T1 - Mechanostimulatory Platform for Improved CAR T Cell Immunotherapy
AU - Yassin, Abed Al Kader
AU - Ureña Martin, Carlos
AU - Le Saux, Guillaume
AU - Pandey, Ashish
AU - Tzadka, Sivan
AU - Toledo, Esti
AU - Pandit, Jatin Jawhir
AU - Sherf, Tomer
AU - Nusbaum, Idan
AU - Bhattachrya, Baisali
AU - Banerji, Rajashri
AU - Greenshpan, Yariv
AU - Abu Ahmad, Muhammad Abu
AU - Radinsky, Olga
AU - Sklartz, Menachem
AU - Gazit, Roi
AU - Elkabets, Moshe
AU - Ghassemi, Sabah
AU - Cohen, Ofir
AU - Schvartzman, Mark
AU - Porgador, Angel
N1 - Publisher Copyright: © 2025 Wiley-VCH GmbH.
PY - 2025/1/1
Y1 - 2025/1/1
N2 - Chimeric Antigen Receptor T (CAR T) cell immunotherapy has revolutionized cancer treatment, yet it is hindered by rapid T-cell exhaustion caused by uncontrolled activation during CAR generation. Leveraging insights into T-cell mechanosensing, a novel mechanostimulatory platform is engineered for T-cell activation based on an antigen-carrying surface with controlled elasticity and nanotopography. The platform is designed to optimize and balance T-cell exhaustion, proliferation, and CAR expression. It enhances the differentiation of T cells into the central memory subset, which is crucial for the persistence of CAR T cell therapy's anticancer effects. The platform produces CAR T cells with higher antitumor efficacy, as validated through ex vivo experiments, and with higher in vivo persistence and ability to suppress tumor proliferation, as compared to CAR T cells generated by standard protocols. RNA-seq analysis confirmed an increased transcriptional signature of central memory T cells. Furthermore, this platform completely eliminates T-cell toxicity associated with the non-viral transfection process typically observed with standard activation methods. This platform presents a promising pathway for improving the efficiency and safety of CAR T cell therapy.
AB - Chimeric Antigen Receptor T (CAR T) cell immunotherapy has revolutionized cancer treatment, yet it is hindered by rapid T-cell exhaustion caused by uncontrolled activation during CAR generation. Leveraging insights into T-cell mechanosensing, a novel mechanostimulatory platform is engineered for T-cell activation based on an antigen-carrying surface with controlled elasticity and nanotopography. The platform is designed to optimize and balance T-cell exhaustion, proliferation, and CAR expression. It enhances the differentiation of T cells into the central memory subset, which is crucial for the persistence of CAR T cell therapy's anticancer effects. The platform produces CAR T cells with higher antitumor efficacy, as validated through ex vivo experiments, and with higher in vivo persistence and ability to suppress tumor proliferation, as compared to CAR T cells generated by standard protocols. RNA-seq analysis confirmed an increased transcriptional signature of central memory T cells. Furthermore, this platform completely eliminates T-cell toxicity associated with the non-viral transfection process typically observed with standard activation methods. This platform presents a promising pathway for improving the efficiency and safety of CAR T cell therapy.
KW - CAR T cells
KW - biomaterials
KW - immunotherapy
KW - mechanosensing
UR - http://www.scopus.com/inward/record.url?scp=105004691982&partnerID=8YFLogxK
U2 - 10.1002/adma.202412482
DO - 10.1002/adma.202412482
M3 - Article
C2 - 40348587
SN - 0935-9648
JO - Advanced Materials
JF - Advanced Materials
ER -