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A cell-engineered system to assess tumor cell sensitivity to CD8+ T cell-mediated cytotoxicity.
Nelson, Nadine; Lopez-Pelaez, Marta; Palazon, Asis; Poon, Edmund; De La Roche, Maike; Barry, Simon; Valge-Archer, Viia; Wilkinson, Robert W; Dovedi, Simon J; Smith, Paul D.
Afiliação
  • Nelson N; Bioscience, Oncology, IMED Biotech Unit, AstraZeneca, Cambridge, UK.
  • Lopez-Pelaez M; Bioscience, Oncology, IMED Biotech Unit, AstraZeneca, Cambridge, UK.
  • Palazon A; Oncology, MedImmune Ltd, Cambridge, UK.
  • Poon E; Oncology, MedImmune Ltd, Cambridge, UK.
  • De La Roche M; Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
  • Barry S; Bioscience, Oncology, IMED Biotech Unit, AstraZeneca, Cambridge, UK.
  • Valge-Archer V; Bioscience, Oncology, IMED Biotech Unit, AstraZeneca, Cambridge, UK.
  • Wilkinson RW; Oncology, MedImmune Ltd, Cambridge, UK.
  • Dovedi SJ; Oncology, MedImmune Ltd, Cambridge, UK.
  • Smith PD; Bioscience, Oncology, IMED Biotech Unit, AstraZeneca, Cambridge, UK.
Oncoimmunology ; 8(8): 1599635, 2019.
Article em En | MEDLINE | ID: mdl-31413906
ABSTRACT
In vitro assays that evaluate CD8+ T cell-mediated cytotoxicity are important to aid in the development of novel therapeutic approaches to enhance anti-tumor immune responses. Here, we describe a novel cytotoxicity co-culture assay that circumvents the problem of highly variable allogeneic responses and obviates the constraints of HLA-restriction between effector and target cells. We show that this assay can be easily applied to a panel of tumor cell lines to provide additional insights into intrinsic drivers of sensitivity/resistance to T cell-mediated killing, and to evaluate the impact of targeted therapies on both tumor and T cell compartments.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article