% IMPORTANT: The following is UTF-8 encoded. This means that in the presence % of non-ASCII characters, it will not work with BibTeX 0.99 or older. % Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or % “biber”. @INBOOK{Mansour:177487, author = {P. Mansour$^*$ and I. Quiros Fernandez$^*$ and E. Fakhr$^*$ and A. Cid-Arregui$^*$}, title = {{G}eneration of {CAR}-{T} cells using lentiviral vectors}, address = {United States}, publisher = {Academic Press Inc.}, reportid = {DKFZ-2021-02574}, pages = {-}, year = {2021}, comment = {Methods in Cell Biology}, booktitle = {Methods in Cell Biology}, abstract = {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 $characterization.https://reader.elsevier.com/reader/sd/pii/S0091679X21000844?token=19B8578AB0A842C9E0A423517A3E8821C298512484E57C501C77B440E558856281E370B178DDAB9F208EBEE22E875043\&originRegion=eu-west-1\&originCreation=20211118072303$}, cin = {D122}, cid = {I:(DE-He78)D122-20160331}, pnm = {314 - Immunologie und Krebs (POF4-314)}, pid = {G:(DE-HGF)POF4-314}, typ = {PUB:(DE-HGF)7}, url = {https://inrepo02.dkfz.de/record/177487}, }