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- W2924339726 abstract "Chimeric antigen receptor (CAR)-engineered T cells have a proven efficacy for the treatment of refractory hematological B cell malignancies. While often accompanied by side effects, CAR-T technology is getting more mature and will become an important treatment option for various tumor indications. In this review, we summarize emerging approaches that aim to further evolve CAR-T cell therapy based on combinations of so-called universal or modular CAR-(modCAR-)T cells, and their respective adaptor molecules (CAR-adaptors), which mediate the crosslinking between target and effector cells. The activity of such modCAR-T cells is entirely dependent on binding of the respective CAR-adaptor to both a tumor antigen and to the CAR-expressing T cell. Contrary to conventional CAR-T cells, where the immunological synapse is established by direct interaction of CAR and membrane-bound target, modCAR-T cells provide a highly flexible and customizable development of the CAR-T cell concept and offer an additional possibility to control T cell activity." @default.
- W2924339726 created "2019-04-01" @default.
- W2924339726 creator A5030197126 @default.
- W2924339726 creator A5050281853 @default.
- W2924339726 creator A5060997883 @default.
- W2924339726 creator A5086363877 @default.
- W2924339726 date "2019-04-17" @default.
- W2924339726 modified "2023-10-16" @default.
- W2924339726 title "Combining the best of two worlds: highly flexible chimeric antigen receptor adaptor molecules (CAR-adaptors) for the recruitment of chimeric antigen receptor T cells" @default.
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- W2924339726 doi "https://doi.org/10.1080/19420862.2019.1596511" @default.
- W2924339726 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6601549" @default.
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- W2924339726 hasPublicationYear "2019" @default.
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