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In vitro re-challenge of CAR T cells.
Klee, Clara Helena; Villatoro, Alicia; Casey, Nicholas Paul; Inderberg, Else Marit; Wälchli, Sébastien.
Afiliação
  • Klee CH; Translational Research Unit, Section of Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway.
  • Villatoro A; Translational Research Unit, Section of Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway.
  • Casey NP; Translational Research Unit, Section of Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway.
  • Inderberg EM; Translational Research Unit, Section of Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway.
  • Wälchli S; Translational Research Unit, Section of Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway. Electronic address: sebastw@rr-research.no.
Methods Cell Biol ; 183: 335-353, 2024.
Article em En | MEDLINE | ID: mdl-38548418
ABSTRACT
Chimeric antigen receptor (CAR) T cells (CAR T) have emerged as a potential therapy for cancer patients. CAR T cells are capable of recognizing membrane proteins on cancer cells which initiates a downstream signaling in T cells that ends in cancer cell death. Continuous antigen exposure over time, activation of inhibitory signaling pathways and/or chronic inflammation can lead to CAR T cell exhaustion. In this context, the design of CARs can have a great impact on the functionality of CAR T cells, on their potency and exhaustion. Here, using CD19CAR as model, we provide a re-challenge protocol where CAR T cells are cultured weekly with malignant lymphoid cell lines BL-41 and Nalm-6 to simulate them with continuous antigen pressure over a four-week period. This protocol can be value for assessing CAR T cell functionality and for the comparison of different CAR constructs.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Linfócitos T / Transdução de Sinais Limite: Humans Idioma: En Revista: Methods Cell Biol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Noruega

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Linfócitos T / Transdução de Sinais Limite: Humans Idioma: En Revista: Methods Cell Biol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Noruega