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STAR Protoc ; 5(1): 102898, 2024 Mar 15.
Article in English | MEDLINE | ID: mdl-38367235

ABSTRACT

The efficacy of chimeric antigen receptor (CAR) T cell immunotherapy is limited by insufficient infiltration and activation of T cells due to the immunosuppressive tumor microenvironment. Preclinical studies with optimized mouse CAR T cells in immunocompetent mouse cancer models will help define the mechanisms underlying immunotherapy resistance. Here, we present a protocol for preparing mouse T cells and generating CAR T cells. We then detail procedures for testing their therapeutic efficacy and tracking them in a syngeneic mouse glioma model. For complete details on the use and execution of this protocol, please refer to Zhang et al.1.


Subject(s)
Glioma , Receptors, Chimeric Antigen , Animals , Mice , Immunotherapy, Adoptive/methods , Receptors, Chimeric Antigen/genetics , Immunotherapy , T-Lymphocytes , Glioma/therapy , Disease Models, Animal , Tumor Microenvironment
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