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Quantitative Imaging Approaches to Study the CAR Immunological Synapse.
Mukherjee, Malini; Mace, Emily M; Carisey, Alexandre F; Ahmed, Nabil; Orange, Jordan S.
Afiliação
  • Mukherjee M; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77025, USA; Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77025, USA; Center for Human Immunobiology, Texas Children's Hospital, Houston, TX 77030, USA. Electronic address: mmukherj@bcm.edu.
  • Mace EM; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77025, USA; Center for Human Immunobiology, Texas Children's Hospital, Houston, TX 77030, USA.
  • Carisey AF; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77025, USA; Center for Human Immunobiology, Texas Children's Hospital, Houston, TX 77030, USA.
  • Ahmed N; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77025, USA; Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77025, USA.
  • Orange JS; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77025, USA; Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77025, USA; Center for Human Immunobiology, Texas Children's Hospital, Houston, TX 77030, USA.
Mol Ther ; 25(8): 1757-1768, 2017 08 02.
Article em En | MEDLINE | ID: mdl-28663103
The lytic immunological synapse (IS) is a discrete structural entity formed after the ligation of specific activating receptors that leads to the destruction of a cancerous cell. The formation of an effector cell IS in cytotoxic T lymphocytes or natural killer cells is a hierarchical and stepwise rearrangement of structural and signaling components and targeted release of the contents of lytic granules. While recent advances in the generation and testing of cytotoxic lymphocytes expressing chimeric antigen receptors (CARs) has demonstrated their efficacy in the targeted lysis of tumor targets, the contribution and dynamics of IS components have not yet been extensively investigated in the context of engineered CAR cells. Understanding the biology of the CAR IS will be a powerful approach to efficiently guide the engineering of new CARs and help identify mechanistic problems in existing CARs. Here, we review the formation of the lytic IS and describe quantitative imaging-based measurements using multiple microscopy techniques at a single cell level that can be used in conjunction with established population-based assays to provide insight into the important cytotoxic function of CAR cells. The inclusion of this approach in the pipeline of CAR product design could be a novel and valuable innovation for the field.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes de Fusão / Receptores de Antígenos de Linfócitos T / Linfócitos T Citotóxicos / Sinapses Imunológicas / Imagem Molecular Limite: Animals / Humans Idioma: En Revista: Mol Ther Assunto da revista: BIOLOGIA MOLECULAR / TERAPEUTICA Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes de Fusão / Receptores de Antígenos de Linfócitos T / Linfócitos T Citotóxicos / Sinapses Imunológicas / Imagem Molecular Limite: Animals / Humans Idioma: En Revista: Mol Ther Assunto da revista: BIOLOGIA MOLECULAR / TERAPEUTICA Ano de publicação: 2017 Tipo de documento: Article