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Abstract

Hematopoietic stem cells (HSCs) transplantation has been the potential treatment for hematopoietic disorder patients. However, once they were prescribed HSCs transplantation as the therapy, especially allogeneic transplantation, they would face Graft versus Host disease (GvHD), which causes by the presence of T cells in donor tissue. To deal with the risk of GvHD, removal T cells in donor tissue prior to transplant to recipient is extremely indispensable. Nowadays, MACS technique using immuno-magnetic nanoparticles in order to deplete T cells shows potential solution in the transplantation. In this study, we prepared immuno-magnetic nanoparticles for separation of Jurkat T cells from cell culture. Anti-Jurkat T antibodies were conjugated onto magnetic nanoparticles via recombinant protein A/G, an antibody’s Fc specific binding protein. The bonds between protein A/G and immuno-magnetic nanoparticles were covalently linked by amine groups on the surface of magnetic nanoparticles and the protein through 3-(2 pyridyldithio) propionic acid N hydroxysuccinimide ester (SPDP). Approximately 85 μg of protein A/G and 21 μg of antibody were bound to one mg of magnetic beads. The immuno-magnetic nanoparticles were capable of isolating up to 53.3% of Jurkat T cells from culture medium.



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Article Details

Issue: Vol 3 No 2 (2019)
Page No.: 74-81
Published: Aug 6, 2019
Section: Original Research
DOI: https://doi.org/10.32508/stdjns.v3i2.802

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Creative Commons License

Copyright: The Authors. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 4.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 How to Cite
Huynh, K.-Q., Tran, T. V., Tran-Nguyen, T.-S., Ta, K.-H. T., & Tran-Van, H. (2019). Genaration and assessment of immunomagnetic nanoparticles capable of T-cell removal. Science and Technology Development Journal - Natural Sciences, 3(2), 74-81. https://doi.org/https://doi.org/10.32508/stdjns.v3i2.802

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