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Genetically Modified T Cells for the Treatment of Malignant Disease

期刊

TRANSFUSION MEDICINE AND HEMOTHERAPY
卷 40, 期 6, 页码 388-402

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KARGER
DOI: 10.1159/000357163

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Adoptive cell transfer; Chimeric antigen receptor; CAR; T-cell receptor; TCR; Clinical trial

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The broaden application of adoptive T-cell transfer has been constrained by the technical abilities to isolate and expand antigen-specific T cells potent to selectively kill tumor cells. With the recent progress in the design and manufacturing of cellular products, T cells used in the treatment of malignant diseases may be regarded as anticancer biopharmaceuticals. Genetical manipulation of T cells has given T cells desired specificity but also enable to tailor their activation and proliferation potential. Here, we summarize the recent developments in genetic engineering of T-cell-based biopharmaceuticals, covering criteria for their clinical application in regard to safety and efficacy.

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