Assessment of chimeric antigen receptor T cytotoxicity by droplet microfluidics in vitro

Author:

Wong Kuan Un1,Shi Jingxuan234,Li Peng235,Wang Haitao1,Jia Yanwei167,Deng Chuxia1,Jiang Lianmei8,Wong Ada Hang-Heng1ORCID

Affiliation:

1. Cancer Centre, Faculty of Health Sciences, University of Macau, Macau SAR, China

2. 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

3. 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

4. University of Chinese Academy of Sciences, Shijingshan District, Beijing 100049, China

5. Guangzhou Regenerative Medicine and Health Guangdong Laboratory, Guangzhou, Guangdong 510005, China

6. State Key Laboratory of Analog and Mixed Signal VLSI, University of Macau, Macau SAR, China

7. Faculty of Science and Technology, University of Macau, Macau SAR, China

8. Department of Molecular Sciences, ARC Excellence Centre for Nanoscale BioPhotonics (CNBP), Macquarie University, Sydney, NSW 2109, Australia

Abstract

Abstract 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.

Funder

Science and Technology Development Fund

Chinese Academy of Sciences

Guangdong Provincial Applied Science and Technology Research and Development Program

Guangzhou Science and Technology Plan

Frontier Research Program of Guangzhou Regenerative Medicine and Health Guangdong Laboratory

UM Chair Professor

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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