2023
DOI: 10.1007/s12094-023-03122-8
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Chimeric antigen receptor T cells therapy in solid tumors

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Cited by 2 publications
(1 citation statement)
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“…Their extracellular domain is usually an scFv capable of specifically binding antigens overexpressed at the surface of tumor cells, linked to a hinge domain (e.g., CD8, CD28, IgG1, or IgG4) and a transmembrane domain (e.g., CD28, 4-1BB or CD8), fused to one or more variable intracellular costimulatory domains (e.g., CD28, 4-1BB, or OX40 -not present in first generation CARs) and a CD3ζ activation domain, leading to full T cell activation after contact with the target antigen [27]. CAR-T cell therapy has led to significant advances in cancer cell immunotherapy, resulting in great success in treating hematological malignancies [79], with recent advances for solid tumor treatments [80], including RCC [81].…”
Section: Chimeric Antigen Receptor (Car) T Cellsmentioning
confidence: 99%
“…Their extracellular domain is usually an scFv capable of specifically binding antigens overexpressed at the surface of tumor cells, linked to a hinge domain (e.g., CD8, CD28, IgG1, or IgG4) and a transmembrane domain (e.g., CD28, 4-1BB or CD8), fused to one or more variable intracellular costimulatory domains (e.g., CD28, 4-1BB, or OX40 -not present in first generation CARs) and a CD3ζ activation domain, leading to full T cell activation after contact with the target antigen [27]. CAR-T cell therapy has led to significant advances in cancer cell immunotherapy, resulting in great success in treating hematological malignancies [79], with recent advances for solid tumor treatments [80], including RCC [81].…”
Section: Chimeric Antigen Receptor (Car) T Cellsmentioning
confidence: 99%