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      High-Throughput Microfluidic 3D Cytotoxicity Assay for Cancer Immunotherapy (CACI-IMPACT Platform)

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          Abstract

          Adoptive cell transfer against solid tumors faces challenges to overcome tumor microenvironment (TME), which plays as a physical barrier and provides immuno-suppressive conditions. Classical cytotoxicity assays are widely used to measure killing ability of the engineered cytotoxic lymphocytes as therapeutics, but the results cannot represent the performance in clinical application due to the absence of the TME. This paper describes a 3D cytotoxicity assay using an injection molded plastic array culture (CACI-IMPACT) device for 3D cytotoxicity assay to assess killing abilities of cytotoxic lymphocytes in 3D microenvironment through a spatiotemporal analysis of the lymphocytes and cancer cells embedded in 3D extra cellular matrix (ECM). Rail-based microfluidic design was integrated within a single 96-well and the wells were rectangularly arrayed in 2 × 6 to enhance the experimental throughput. The rail-based microstructures facilitate hydrogel patterning with simple pipetting so that hydrogel pre-solution aspirated with 10 μl pipette can be patterned in 10 wells within 30 s. To demonstrate 3D cytotoxicity assay, we patterned HeLa cells encapsulated by collagen gel and observed infiltration, migration and cytotoxic activity of NK-92 cells against HeLa cells in the collagen matrix. We found that 3D ECM significantly reduced migration of cytotoxic lymphocytes and access to cancer cells, resulting in lower cytotoxicity compared with 2D assays. In dense ECM, the physical barrier function of the 3D matrix was enhanced, but the cytotoxic lymphocytes effectively killed cancer cells once they contacted with cancer cells. The results implied ECM significantly influences migration and cytotoxicity of cytotoxic lymphocytes. Hence, the CACI-IMPACT platform, enabling high-throughput 3D co-culture of cytotoxic lymphocyte with cancer cells, has the potential to be used for pre-clinical evaluation of cytotoxic lymphocytes engineered for immunotherapy against solid tumors.

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          Most cited references17

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          The Principles of Engineering Immune Cells to Treat Cancer

          Chimeric antigen receptor (CAR) T cells have proven that engineered immune cells can serve as a powerful new class of cancer therapeutics. Clinical experience has helped to define the major challenges that must be met to make engineered T cells a reliable, safe, and effective platform that can be deployed against a broad range of tumors. The emergence of synthetic biology approaches for cellular engineering is providing us with a broadly expanded set of tools for programming immune cells. We discuss how these tools could be used to design the next generation of smart T cell precision therapeutics.
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            Obstacles Posed by the Tumor Microenvironment to T cell Activity: A Case for Synergistic Therapies.

            T cell dysfunction in solid tumors results from multiple mechanisms. Altered signaling pathways in tumor cells help produce a suppressive tumor microenvironment enriched for inhibitory cells, posing a major obstacle for cancer immunity. Metabolic constraints to cell function and survival shape tumor progression and immune cell function. In the face of persistent antigen, chronic T cell receptor signaling drives T lymphocytes to a functionally exhausted state. Here we discuss how the tumor and its microenvironment influences T cell trafficking and function with a focus on melanoma, and pancreatic and ovarian cancer, and discuss how scientific advances may help overcome these hurdles.
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              Engineering of functional, perfusable 3D microvascular networks on a chip.

              Generating perfusable 3D microvessels in vitro is an important goal for tissue engineering, as well as for reliable modelling of blood vessel function. To date, in vitro blood vessel models have not been able to accurately reproduce the dynamics and responses of endothelial cells to grow perfusable and functional 3D vascular networks. Here we describe a microfluidic-based platform whereby we model natural cellular programs found during normal development and angiogenesis to form perfusable networks of intact 3D microvessels as well as tumor vasculatures based on the spatially controlled co-culture of endothelial cells with stromal fibroblasts, pericytes or cancer cells. The microvessels possess the characteristic morphological and biochemical markers of in vivo blood vessels, and exhibit strong barrier function and long-term stability. An open, unobstructed microvasculature allows the delivery of nutrients, chemical compounds, biomolecules and cell suspensions, as well as flow-induced mechanical stimuli into the luminal space of the endothelium, and exhibits faithful responses to physiological shear stress as demonstrated by cytoskeleton rearrangement and increased nitric oxide synthesis. This simple and versatile platform provides a wide range of applications in vascular physiology studies as well as in developing vascularized organ-on-a-chip and human disease models for pharmaceutical screening.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                28 May 2019
                2019
                : 10
                : 1133
                Affiliations
                [1] 1Division of WCU Multiscale Mechanical Design, Seoul National University , Seoul, South Korea
                [2] 2Department of Electrical Engineering and Computer Science, Seoul National University , Seoul, South Korea
                [3] 3Department of Materials Science and Engineering, Seoul National University , Seoul, South Korea
                [4] 4Department of Mechanical and Aerospace Engineering, Seoul National University , Seoul, South Korea
                [5] 5Institute of Bioengineering, Seoul National University , Seoul, South Korea
                [6] 6Institute of Advanced Machines and Design , Seoul, South Korea
                Author notes

                Edited by: Leila Akkari, The Netherlands Cancer Institute (NKI), Netherlands

                Reviewed by: Per thor Straten, Herlev Hospital, Denmark; Subramaniam Malarkannan, Medical College of Wisconsin, United States

                *Correspondence: Junsang Doh jsdoh@ 123456snu.ac.kr

                This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2019.01133
                6546835
                31191524
                02c6f02d-89e4-4748-b631-b0ffc2d402d5
                Copyright © 2019 Park, Son, Hwang, Ko, Lee, Doh and Jeon.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 16 February 2019
                : 07 May 2019
                Page count
                Figures: 4, Tables: 0, Equations: 0, References: 33, Pages: 9, Words: 6081
                Funding
                Funded by: Ministry of Trade, Industry and Energy 10.13039/501100003052
                Award ID: NRF-2015M3A9D7051910
                Award ID: NRF-2018R1A2A1A05019550
                Award ID: NRF-2017R1A2B3006006
                Award ID: N0002239
                Categories
                Immunology
                Original Research

                Immunology
                cytotoxicity assay,microfluidics,cancer immunotherapy,cytotoxic lymphocytes,high-throughput screening

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