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Assessment of chimeric antigen receptor T cytotoxicity by droplet microfluidics in vitro.
Wong, Kuan Un; Shi, Jingxuan; Li, Peng; Wang, Haitao; Jia, Yanwei; Deng, Chuxia; Jiang, Lianmei; Wong, Ada Hang-Heng.
Afiliação
  • Wong KU; Cancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR, China.
  • Shi J; Key Laboratory of Regenerative Biology, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, Guangdong 510530, China.
  • Li P; Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, Guangdong 510530, China.
  • Wang H; University of Chinese Academy of Sciences, Shijingshan District, Beijing 100049, China.
  • Jia Y; Key Laboratory of Regenerative Biology, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, Guangdong 510530, China.
  • Deng C; Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, Guangdong 510530, China.
  • Jiang L; Guangzhou Regenerative Medicine and Health Guangdong Laboratory, Guangzhou, Guangdong 510005, China.
  • Wong AH; Cancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR, China.
Antib Ther ; 5(2): 85-99, 2022 Apr.
Article em En | MEDLINE | ID: mdl-35441124
Chimeric antigen receptor T (CAR-T) cells are cytotoxic T cells engineered to specifically kill cancer cells expressing specific target receptor(s). Prior CAR-T efficacy tests include CAR expression analysis by qPCR or ELISA, in vitro measurement of interferon-γ (IFNγ) or interleukin-2 (IL-2), and xenograft models. However, the in vitro measurements did not reflect CAR-T cytotoxicity, whereas xenograft models are low throughput and costly. Here, we presented a robust in vitro droplet microfluidic assay for CAR-T cytotoxicity assessment. This method not only enabled assessment of CAR-T cytotoxic activity under different fluid viscosity conditions, but also facilitated measurement of CAR-T expansion and dissection of mechanism of action via phenotype analysis in vitro. Furthermore, our data suggested that label-free cytotoxicity analysis is feasible by acquiring data before and after treatment. Hence, this study presented a novel in vitro method for assessment of cellular cytotoxicity that could potentially be applied to any cytotoxicity experiment with varying solvent composition.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Antib Ther Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Antib Ther Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China