TY - CHAP
T1 - In Vitro Generation of Stem Cell Memory-Like T Cells from Activated T Cells
AU - Ando, Makoto
AU - Ikeda, Mari
AU - Yoshimura, Akihiko
AU - Kondo, Taisuke
N1 - Publisher Copyright:
© 2020, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2020
Y1 - 2020
N2 - Adoptive T-cell therapy is an attractive strategy for cancer immunotherapy. The transfer of in vitro expanded tumor-associated antigen (TAA)-specific T cells from patients may effectively fight against the original tumor cells. The chimeric antigen receptor-engineered T (CAR-T) cells are also shown to be a promising therapy for hematologic malignancies. However, one of the limitations of these T-cell-based therapies is a rapid acquisition of tolerant (anergy, deletion, dysfunctional and/or exhausted) phenotypes of T cells during activation in vitro and/or after transfer in vivo. We and others found that stem cell memory T (TSCM) cells are strongly resistant against such tolerance, showing strong expansion and persistence in vivo, and provide long-lasting antitumor effects. Here we describe a protocol for the generation of phenotypically TSCM-like cells (iTSCM cells), which can be induced by simple co-culture of activated T cells with OP9 stroma cells expressing a Notch ligand. We also showed the methods of cancer immunotherapy by using NSG mice.
AB - Adoptive T-cell therapy is an attractive strategy for cancer immunotherapy. The transfer of in vitro expanded tumor-associated antigen (TAA)-specific T cells from patients may effectively fight against the original tumor cells. The chimeric antigen receptor-engineered T (CAR-T) cells are also shown to be a promising therapy for hematologic malignancies. However, one of the limitations of these T-cell-based therapies is a rapid acquisition of tolerant (anergy, deletion, dysfunctional and/or exhausted) phenotypes of T cells during activation in vitro and/or after transfer in vivo. We and others found that stem cell memory T (TSCM) cells are strongly resistant against such tolerance, showing strong expansion and persistence in vivo, and provide long-lasting antitumor effects. Here we describe a protocol for the generation of phenotypically TSCM-like cells (iTSCM cells), which can be induced by simple co-culture of activated T cells with OP9 stroma cells expressing a Notch ligand. We also showed the methods of cancer immunotherapy by using NSG mice.
KW - Adoptive T-cell therapy
KW - Co-culture with feeder cells
KW - EB virus-specific T cells
KW - NSG mice
KW - Notch signaling
KW - Stem cell memory T cells
UR - http://www.scopus.com/inward/record.url?scp=85077785719&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85077785719&partnerID=8YFLogxK
U2 - 10.1007/978-1-0716-0266-9_11
DO - 10.1007/978-1-0716-0266-9_11
M3 - Chapter
C2 - 31933204
AN - SCOPUS:85077785719
T3 - Methods in Molecular Biology
SP - 127
EP - 139
BT - Methods in Molecular Biology
PB - Humana Press Inc.
ER -