Your browser doesn't support javascript.
loading
Efficient Generation of Murine Chimeric Antigen Receptor (CAR)-T Cells.
Vincent, Rosa L; Li, Fangda; Ballister, Edward R; Arpaia, Nicholas; Danino, Tal.
Afiliação
  • Vincent RL; Department of Biomedical Engineering, Columbia University.
  • Li F; Department of Microbiology & Immunology, Vagelos College of Physicians and Surgeons, Columbia University.
  • Ballister ER; Department of Biomedical Engineering, Columbia University.
  • Arpaia N; Department of Microbiology & Immunology, Vagelos College of Physicians and Surgeons, Columbia University; Herbert Irving Comprehensive Cancer Center, Columbia University.
  • Danino T; Department of Biomedical Engineering, Columbia University; Herbert Irving Comprehensive Cancer Center, Columbia University; Data Science Institute, Columbia University; td2506@columbia.edu.
J Vis Exp ; (204)2024 Feb 02.
Article em En | MEDLINE | ID: mdl-38372353
ABSTRACT
Engineered cell therapies utilizing chimeric antigen receptor (CAR)-T cells have achieved remarkable effectiveness in individuals with hematological malignancies and are presently undergoing development for the treatment of diverse solid tumors. So far, the preliminary evaluation of novel CAR-T cell products has predominantly taken place in xenograft tumor models using immunodeficient mice. This approach is chosen to facilitate the successful engraftment of human CAR-T cells in the experimental setting. However, syngeneic mouse models, in which tumors and CAR-T cells are derived from the same mouse strain, allow evaluation of new CAR technologies in the context of a functional immune system and comprehensive tumor microenvironment (TME). The protocol described here aims to streamline the process of mouse CAR-T cell generation by presenting standardized methods for retroviral transduction and ex vivo T cell culture. The methods described in this protocol can be applied to other CAR constructs beyond the ones used in this study to enable routine evaluation of new CAR technologies in immune-competent systems.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de Antígenos Quiméricos / Neoplasias Limite: Animals / Humans Idioma: En Revista: J Vis Exp Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de Antígenos Quiméricos / Neoplasias Limite: Animals / Humans Idioma: En Revista: J Vis Exp Ano de publicação: 2024 Tipo de documento: Article