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037 _ _ |a DKFZ-2021-02574
100 1 _ |a Mansour, P.
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245 _ _ |a Generation of CAR-T cells using lentiviral vectors
260 _ _ |a United States
|c 2021
|b Academic Press Inc.
295 1 0 |a Methods in Cell Biology
300 _ _ |a -
336 7 _ |a BOOK_CHAPTER
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336 7 _ |a Book Section
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336 7 _ |a INBOOK
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336 7 _ |a Output Types/Book chapter
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336 7 _ |a Contribution to a book
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520 _ _ |a Cancer immunotherapy is nowadays largely focused on the development of therapeutic antibodies and chimeric antigen receptors (CARs). Two CARs targeting CD19 have been approved recently for the treatment of some hematological malignancies. This demonstrates the capability of engineered CAR T cells in generating effective tumor responses. Furthermore, several hundred ongoing clinical trials are exploring the feasibility of CAR-based approaches to target tumor-associated antigens in solid tumors. However, there still remain significant challenges and limitations in the design and production of CAR-modified T cells that need to be addressed, such as more effective transduction methods, expression and exhaustion issues, reliable in vitro and in vivo characterization methods, etc. Here we describe current techniques for generating CAR T cells using lentiviral vectors as well as detailed protocols for their functional characterization.https://reader.elsevier.com/reader/sd/pii/S0091679X21000844?token=19B8578AB0A842C9E0A423517A3E8821C298512484E57C501C77B440E558856281E370B178DDAB9F208EBEE22E875043&originRegion=eu-west-1&originCreation=20211118072303
536 _ _ |a 314 - Immunologie und Krebs (POF4-314)
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700 1 _ |a Quiros Fernandez, Isaac
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700 1 _ |a Fakhr, Elham
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700 1 _ |a Cid-Arregui, Angel
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910 1 _ |a Deutsches Krebsforschungszentrum
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913 1 _ |a DE-HGF
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|v Immunologie und Krebs
|x 0
914 1 _ |y 2021
920 1 _ |0 I:(DE-He78)D122-20160331
|k D122
|l D122 AG Gezielte Tumorvakzine
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980 _ _ |a contb
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)D122-20160331
980 _ _ |a UNRESTRICTED


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