2019
DOI: 10.1016/j.jcyt.2019.04.013
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Microfluidic purification of T lymphocytes separated from blood for chimeric antigen receptor T-cell manufacturing

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Cited by 3 publications
(2 citation statements)
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“…Rapidly screening for MAbs of surface receptors on breast cancer has been carried out in a microfluidic platform for use in clinical analysis [250]. The microfluidic purification of T lymphocytes separated from blood for chimeric antigen receptor T cell manufacturing has been demonstrated for CAR-T cell therapy reinjection [251], and the gene editing required to manufacture CAR-T cells has also been mechanized by microfluidic devices incorporating electroporation for CRISPR/CAS-9 modification [252]. Profiling T cell interaction and activation through serial encounters with antigen-presenting cells (APCs) has been accomplished in a microfluidic device mimicking the microenvironment of a lymph node [253].…”
Section: Drug Development and Deliverymentioning
confidence: 99%
“…Rapidly screening for MAbs of surface receptors on breast cancer has been carried out in a microfluidic platform for use in clinical analysis [250]. The microfluidic purification of T lymphocytes separated from blood for chimeric antigen receptor T cell manufacturing has been demonstrated for CAR-T cell therapy reinjection [251], and the gene editing required to manufacture CAR-T cells has also been mechanized by microfluidic devices incorporating electroporation for CRISPR/CAS-9 modification [252]. Profiling T cell interaction and activation through serial encounters with antigen-presenting cells (APCs) has been accomplished in a microfluidic device mimicking the microenvironment of a lymph node [253].…”
Section: Drug Development and Deliverymentioning
confidence: 99%
“…One of the most promising technologies is cell viability detection inside a microfluidic chip . At present, there are many common methods for cell viability detection inside a microfluidic chip, such as trypan blue staining, , MTT assay, , and impedance assay. , However, some important technologies of cell viability detection inside a microfluidic chip have not been completely solved until now. One of the most critical technologies is the long-term culture of living cells with normal function, which is one of the bottlenecks in the development of biochip technology.…”
Section: Introductionmentioning
confidence: 99%