3D tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity

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作者
Sneha Gopal
Seok-Joon Kwon
Bosung Ku
Dong Woo Lee
Jungeun Kim
Jonathan S. Dordick
机构
[1] Rensselaer Polytechnic Institute,Department of Chemical and Biological Engineering, and Center for Biotechnology & Interdisciplinary Studies
[2] MBD (Medical & Bio Decision) Co.,Department of Biomedical Engineering
[3] Ltd,Departments of Biomedical Engineering and Biological Sciences
[4] Konyang University,undefined
[5] Rensselaer Polytechnic Institute,undefined
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Immunotherapy has emerged as a promising approach to treating several forms of cancer. Use of immune cells, such as natural killer (NK) cells, along with small molecule drugs and antibodies through antibody dependent cell-mediated cytotoxicity (ADCC) has been investigated as a potential combination therapy for some difficult to treat solid tumors. Nevertheless, there remains a need to develop tools that support co-culture of target cancer cells and effector immune cells in a contextually relevant three-dimensional (3D) environment to provide a rapid means to screen for and optimize ADCC-drug combinations. To that end, here we have developed a high throughput 330 micropillar-microwell sandwich platform that enables 3D co-culture of NK92-CD16 cells with pancreatic (MiaPaCa-2) and breast cancer cell lines (MCF-7 and MDA-MB-231). The platform successfully mimicked hypoxic conditions found in a tumor microenvironment and was used to demonstrate NK-cell mediated cell cytotoxicity in combination with two monoclonal antibodies; Trastuzumab and Atezolizumab. The platform was also used to show dose response behavior of target cancer cells with reduced EC50 values for paclitaxel (an anti-cancer chemotherapeutic) when treated with both NK cells and antibody. Such a platform may be used to develop more personalized cancer therapies using patient-derived cancer cells.
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