Seminars in Hematology, Год журнала: 2024, Номер 61(5), С. 271 - 272
Опубликована: Окт. 1, 2024
Язык: Английский
Seminars in Hematology, Год журнала: 2024, Номер 61(5), С. 271 - 272
Опубликована: Окт. 1, 2024
Язык: Английский
Medical Oncology, Год журнала: 2025, Номер 42(6)
Опубликована: Апрель 24, 2025
Язык: Английский
Процитировано
0Deleted Journal, Год журнала: 2025, Номер 33(1), С. 200949 - 200949
Опубликована: Фев. 11, 2025
Chimeric antigen receptor T cell (CAR-T) therapies have revolutionized cancer immunotherapy. Traditional single-chain variable fragments (ScFvs) used as CAR recognition moieties face challenges such high tonic signaling, compromised binding epitopes, and suboptimal affinity. Single-domain antibodies (SdAbs) offer an attractive alternative due to their smaller size, stability, reduced immunogenicity. In this work, we developed SdAb-CAR-T discovery platform integrating generation, characterization, selection of SdAbs based on various properties. This approach was demonstrated by developing CAR-T cells with against CD33, a target for acute myeloid leukemia (AML). We identified diverse affinities ranging from 3.9-115 nM, characterized kinetics epitope recognition. Using SdAb-based second-generation CARs, assessed phenotypes, cytotoxicity cytokine release in vitro, resulting signaling increased production. vivo, exhibited enhanced efficacy at lower doses, xenograft AML mouse model, demonstrating advantages over ScFv-based CD33 cells.
Язык: Английский
Процитировано
0Seminars in Hematology, Год журнала: 2024, Номер 61(5), С. 271 - 272
Опубликована: Окт. 1, 2024
Язык: Английский
Процитировано
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