2021
DOI: 10.1016/j.beha.2021.101285
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TCR gene-engineered cell therapy for solid tumors

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Cited by 16 publications
(14 citation statements)
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“…T-cell receptor-engineered T-cell (TCR-T) therapy has the advantage of targeting potentially any antigen, not only those expressed on the surface of cells, such as with CAR-T-cells. Recent clinical studies on TCR-T showed meaningful results in solid tumor patients [ 191 , 192 , 193 ], with New York esophageal squamous cell carcinoma-1 (NY-ESO-1) being the most frequently targeted, with a relevant clinical response rate in metastatic melanoma and in metastatic synovial sarcoma patients [ 194 , 195 , 196 ].…”
Section: Tcr and Cancermentioning
confidence: 99%
“…T-cell receptor-engineered T-cell (TCR-T) therapy has the advantage of targeting potentially any antigen, not only those expressed on the surface of cells, such as with CAR-T-cells. Recent clinical studies on TCR-T showed meaningful results in solid tumor patients [ 191 , 192 , 193 ], with New York esophageal squamous cell carcinoma-1 (NY-ESO-1) being the most frequently targeted, with a relevant clinical response rate in metastatic melanoma and in metastatic synovial sarcoma patients [ 194 , 195 , 196 ].…”
Section: Tcr and Cancermentioning
confidence: 99%
“…In summary, TCR-T cell therapy has shown good potential in both preclinical and clinical studies (8,35,102,107,(114)(115)(116). However, clinical trials evaluating TCR-T for CRC are still in their early phases, and the safety and efficacy of these therapies still face many challenges (43).…”
Section: Tcr-t Therapymentioning
confidence: 99%
“…Such antigens may include melanoma antigen recognized by T cells 1 (MART-1), gp100, CEA, New York esophageal squamous cell carcinoma-1 (NY-ESO-1), melanoma-associated antigen A3 (MAGE-A3), melanoma-associated antigen A4 (MAGE-A4), HER2, and CD19 ( 106 ). Due to their high specificities and strong immunogenicities, neoantigens (neoAgs) have been considered the ideal targets for antitumor immunotherapy ( 107 ).…”
Section: Tcr-t Therapymentioning
confidence: 99%
“…However, in the case of CAR-T treatment, CAR-T cells can migrate throughout the body via the blood, which is efficient for spreading cancer-like disorders [2,10,[23][24]. Besides, CAR-T cells can live in the human body for more than ten years, reducing the likelihood of cancer recurrence.…”
Section: Surgical Treatmentmentioning
confidence: 99%
“…However, CIK and other non-specific activated lymphocytes lack tumor-specific response-ability. In this situation, scientists have started to introduce T cell receptor (TCR) or CAR genes that recognize tumor antigens into lymphocytes through genetic modification to make them TCR genemodified T lymphocytes (TCR-T) or CAR-T cells with tumor antigen targeting recognition ability [22,24,25].…”
Section: Tumor-infiltrating Lymphocyte (Til) and T Cell Receptor (Tcr)mentioning
confidence: 99%