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Characterization of CAR T cell expansion and cytotoxic potential during Ex Vivo manufacturing using image-based cytometry.
Maldini, Colby R; Love, Andrea C; Tosh, Kevin W; Chan, Leo Li-Ying; Gayout, Kevin; Smith, Tim; Riley, James L.
Afiliação
  • Maldini CR; Department of Microbiology, Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Love AC; Department of Technology R&D, Nexcelom Bioscience LLC, Lawrence, MA 01843, USA.
  • Tosh KW; Department of Microbiology, Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Chan LL; Department of Technology R&D, Nexcelom Bioscience LLC, Lawrence, MA 01843, USA.
  • Gayout K; Department of Microbiology, Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Smith T; Department of Technology R&D, Nexcelom Bioscience LLC, Lawrence, MA 01843, USA.
  • Riley JL; Department of Microbiology, Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: rileyj@upenn.edu.
J Immunol Methods ; 484-485: 112830, 2020.
Article em En | MEDLINE | ID: mdl-32745474
ABSTRACT
Since the FDA approval of two Chimeric Antigen Receptor (CAR) T cell therapies against CD19+ malignancies, there has been significant interest in adapting CAR technology to other diseases. As such, the ability to simultaneously monitor manufacturing criteria and functional characteristics of multiple CAR T cell products by a single instrument would likely accelerate the development of candidate therapies. Here, we demonstrate that image-based cytometry yields high-throughput measurements of CAR T cell proliferation and size, and captures the kinetics of in vitro antigen-specific CAR T cell-mediated killing. The data acquired and analyzed by the image cytometer are congruent with results derived from conventional technologies when tested contemporaneously. Moreover, the use of bright-field and fluorescence microscopy by the image cytometer provides kinetic measurements and rapid data acquisition, which are direct advantages over industry standard instruments. Together, image cytometry enables fast, reproducible measurements of CAR T cell manufacturing criteria and effector function, which can greatly facilitate the evaluation of novel CARs with therapeutic potential.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T / Leucemia Mieloide / Antígenos CD / Imunoterapia Adotiva / Citotoxicidade Imunológica / Proliferação de Células / Citometria de Fluxo / Receptores de Antígenos Quiméricos / Microscopia de Fluorescência Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Immunol Methods Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T / Leucemia Mieloide / Antígenos CD / Imunoterapia Adotiva / Citotoxicidade Imunológica / Proliferação de Células / Citometria de Fluxo / Receptores de Antígenos Quiméricos / Microscopia de Fluorescência Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Immunol Methods Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos