Profiling T cell interaction and activation through microfluidics-assisted serial encounter with APCs
•Our developed microfluidic device provided the single-cell-level cell-cell interaction.•Ca2+ flux in a T cell was observed and showed the diversity of immune response.•The target cell was able to be retrieved and released by micromanipulator system. Adoptive T cell therapy that collected from the p...
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Published in | Sensors and actuators. B, Chemical Vol. 330; p. 129306 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Lausanne
Elsevier B.V
01.03.2021
Elsevier Science Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | •Our developed microfluidic device provided the single-cell-level cell-cell interaction.•Ca2+ flux in a T cell was observed and showed the diversity of immune response.•The target cell was able to be retrieved and released by micromanipulator system.
Adoptive T cell therapy that collected from the patient’s blood for treating cancer and chronic infections has revolutionized the field of oncology and personalized medicine. However, such highly activated T cells that have specific T cell receptor (TCR) against the target disease are usually greatly outnumbered by not-activated T cells due to the stochastic generation of TCR by V(D)J recombination, approximately 106∼107 possible TCR. In this report, for the purpose of representing the lymph node where T cells can migrate on the surface of the antigen presenting cells (APCs) for activation or sequentially interact to multiple APCs, an open-type PDMS microfluidic device has been developed. This device mimics the microenvironment of a lymph node for the T cells to scan, contact and interact with APC and has the structure for the plan to collect the cells and conduct downstream analysis later on. By measuring and profiling Ca2+ flux of the T cell that interacted with APC, the threshold classifying whether T cells activation is specific or not was calculated. This new tool is expected to be useful in providing new insight and strategy to basic biology. |
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ISSN: | 0925-4005 1873-3077 |
DOI: | 10.1016/j.snb.2020.129306 |