Jui‐Yi Chen

ORCID: 0000-0001-7417-5100
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About
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Research Areas
  • Immunotherapy and Immune Responses
  • Nanoplatforms for cancer theranostics
  • Monoclonal and Polyclonal Antibodies Research
  • Immune Cell Function and Interaction
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • CAR-T cell therapy research
  • RNA Interference and Gene Delivery

University of California, Irvine
2022-2023

Academia Sinica
2021

Institute of Biomedical Sciences, Academia Sinica
2021

In this study, efficient T cell activation is demonstrated using cell-sized artificial antigen-presenting cells (aAPCs) with protein-conjugated bilayer lipid membranes that mimic biological membranes. The highly uniform aAPCs are generated by a facile method based on standard droplet microfluidic devices. These able to activate the in peripheral blood mononuclear cells, showing 28-fold increase interferon gamma (IFNγ) secretion, 233-fold antigen-specific CD8 expansion, and 16-fold of CD4...

10.1002/adhm.202203163 article EN cc-by-nc-nd Advanced Healthcare Materials 2023-01-16

The growing enthusiasm for cancer immunotherapies and adoptive cell therapies has prompted increasing interest in biomaterials development mimicking natural antigen-presenting cells (APCs) T-cell expansion. In contrast to conventional bottom-up approaches aimed at layering synthetic substrates with activation cues, transformation of live dendritic (DCs) into artificial APCs (aAPCs) is demonstrated herein using a facile minimally disruptive hydrogelation technique. Through direct...

10.1002/adma.202101190 article EN Advanced Materials 2021-06-07

Abstract In this study, efficient T cell activation is demonstrated using cell-sized artificial antigen-presenting cells (aAPCs) with protein-conjugated bilayer lipid membranes that mimic biological membranes. The highly uniform aAPCs are generated by a facile method based on standard droplet microfluidic devices. These able to activate the in peripheral blood mononuclear (PBMCs), showing 28-fold increase IFNγ secretion, 233-fold antigen-specific CD8 expansion, and 16-fold of CD4 expansion....

10.1101/2022.12.02.518936 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-12-03

Robust and modular systems for T cell expansion have immense utilities clinical development immunoengineering research. In article 2101190, Che-Ming J. Hu co-workers demonstrate a photoactivated intracellular radical polymerization technique that transforms live dendritic cells into functional T-cell-stimulating biomaterial, which effectively enhances adoptive therapy against cancer in mice.

10.1002/adma.202170232 article EN Advanced Materials 2021-07-01
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