A straightforward microfluidic-based approach toward optimizing transduction efficiency of HIV-1-derived lentiviral vectors in BCP-ALL cells

Biotechnology Reports - Tập 38 - Trang e00792 - 2023
Seyed Esmaeil Ahmadi1, Rima Manafi Shabestari1, Amir Asri kojabad1, Majid Safa1
1Department of Hematology and Blood Banking, Faculty of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran

Tài liệu tham khảo

Mascarenhas, 1998, Gene delivery to human B-precursor acute lymphoblastic leukemia cells, Blood, 92, 3537, 10.1182/blood.V92.10.3537.422k52_3537_3545 Mock, 2012, Efficient lentiviral transduction and transgene expression in primary human B cells, Hum. Gene. Ther. Methods, 23, 408, 10.1089/hgtb.2012.160 Swainson, 2008, Lentiviral transduction of immune cells, Methods Mol. Biol., 415, 301 Gouvarchin Ghaleh, 2020, Concise review on optimized methods in production and transduction of lentiviral vectors in order to facilitate immunotherapy and gene therapy, Biomed. Pharmacotherapy, 128, 10.1016/j.biopha.2020.110276 Naldini, 1996, In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector, Science, 272, 263, 10.1126/science.272.5259.263 Frankel, 1998, HIV-1: fifteen proteins and an RNA, Annu. Rev. Biochem., 67, 1, 10.1146/annurev.biochem.67.1.1 Walther, 2000, Viral vectors for gene transfer: a review of their use in the treatment of human diseases, Drugs, 60, 249, 10.2165/00003495-200060020-00002 Milone, 2018, Clinical use of lentiviral vectors, Leukemia, 32, 1529, 10.1038/s41375-018-0106-0 Davis, 2002, Polybrene increases retrovirus gene transfer efficiency by enhancing receptor-independent virus adsorption on target cell membranes, Biophys. Chem., 97, 159, 10.1016/S0301-4622(02)00057-1 O'Doherty, 2000, Human immunodeficiency virus type 1 spinoculation enhances infection through virus binding, J. Virol., 74, 10074, 10.1128/JVI.74.21.10074-10080.2000 Lee, 2009, Retronectin enhances lentivirus-mediated gene delivery into hematopoietic progenitor cells, Biologicals, 37, 203, 10.1016/j.biologicals.2009.01.008 Wang, 2014, Rapamycin relieves lentiviral vector transduction resistance in human and mouse hematopoietic stem cells, Blood, 124, 913, 10.1182/blood-2013-12-546218 Deng, 2014, The effect of dexamethasone on lentiviral vector infection is associated with importin α, Biomed. Rep., 2, 137, 10.3892/br.2013.194 Sutlu, 2012, Inhibition of intracellular antiviral defense mechanisms augments lentiviral transduction of human natural killer cells: implications for gene therapy, Hum. Gene Ther., 23, 1090, 10.1089/hum.2012.080 Petrillo, 2018, Cyclosporine H overcomes innate immune restrictions to improve lentiviral transduction and gene editing in human hematopoietic stem cells, Cell Stem Cell, 23, 820, 10.1016/j.stem.2018.10.008 Lewis, 2018, Staurosporine increases lentiviral vector transduction efficiency of human hematopoietic stem and progenitor cells, Mol. Therapy-Methods & Clin. Dev., 9, 313, 10.1016/j.omtm.2018.04.001 Johnston, 2014, High-throughput screening identifies compounds that enhance lentiviral transduction, Gene Ther., 21, 1008, 10.1038/gt.2014.80 Uchida, 2019, High-efficiency lentiviral transduction of human CD34+ cells in high-density culture with poloxamer and prostaglandin E2, Mol. Therapy-Methods & Clin. Dev., 13, 187, 10.1016/j.omtm.2019.01.005 Chuck, 1996, Retroviral infection is limited by Brownian motion, Hum. Gene Ther., 7, 1527, 10.1089/hum.1996.7.13-1527 Higashikawa, 2001, Kinetic analyses of stability of simple and complex retroviral vectors, Virology, 280, 124, 10.1006/viro.2000.0743 Zhang, 2004, The significance of controlled conditions in lentiviral vector titration and in the use of multiplicity of infection (MOI) for predicting gene transfer events, Genet Vaccines Ther., 2 Andreadis, 2000, Toward a more accurate quantitation of the activity of recombinant retroviruses: alternatives to titer and multiplicity of infection, J. Virol., 74, 1258, 10.1128/JVI.74.3.1258-1266.2000 Sutton, 2016, Bioengineering and serum free expansion of blood-derived γδ T cells, Cytotherapy, 18, 881, 10.1016/j.jcyt.2016.04.001 Haas, 2000, Critical factors influencing stable transduction of human CD34(+) cells with HIV-1-derived lentiviral vectors, Mol. Ther., 2, 71, 10.1006/mthe.2000.0094 Brown, 2020, An improved protocol for the production of lentiviral vectors, STAR Protocols, 1, 10.1016/j.xpro.2020.100152 Jiang, 2015, An optimized method for high-titer lentivirus preparations without ultracentrifugation, Sci. Rep., 5, 13875, 10.1038/srep13875 Tran, 2017, Microfluidic transduction harnesses mass transport principles to enhance gene transfer efficiency, Mol. Ther., 25, 2372, 10.1016/j.ymthe.2017.07.002 Tran, 2020, Microfluidic approach for highly efficient viral transduction, Methods Mol. Biol., 2097, 55, 10.1007/978-1-0716-0203-4_3 Strober, 2015, Trypan blue exclusion test of cell viability, Curr. Protoc. Immunol., 111, 10.1002/0471142735.ima03bs111 Morgan, 1995, Retrovirus infection: effect of time and target cell number, J Virol, 69, 6994, 10.1128/jvi.69.11.6994-7000.1995 Tayi, 2010, Mathematical model of the rate-limiting steps for retrovirus-mediated gene transfer into mammalian cells, Biotechnol. Bioeng., 105, 195, 10.1002/bit.22515 Amirache, 2014, Mystery solved: vSV-G-LVs do not allow efficient gene transfer into unstimulated T cells, B cells, and HSCs because they lack the LDL receptor, Blood, 123, 1422, 10.1182/blood-2013-11-540641 Sun, 2010, Internalization and fusion mechanism of vesicular stomatitis virus and related rhabdoviruses, Future Virol., 5, 85, 10.2217/fvl.09.72 Davis, 2002, Polybrene increases retrovirus gene transfer efficiency by enhancing receptor-independent virus adsorption on target cell membranes, Biophys. Chem., 97, 159, 10.1016/S0301-4622(02)00057-1 Chuck, 1996, Consistent and high rates of gene transfer can be obtained using flow-through transduction over a wide range of retroviral titers, Hum. Gene Ther., 7, 743, 10.1089/hum.1996.7.6-743 Moore, 2019, A microfluidic device to enhance viral transduction efficiency during manufacture of engineered cellular therapies, Sci. Rep., 9, 15101, 10.1038/s41598-019-50981-9 Luni, 2013, Stochastic model-assisted development of efficient low-dose viral transduction in microfluidics, Biophys. J., 104, 934, 10.1016/j.bpj.2012.12.049 Silva, 2016, Highly efficient adenoviral transduction of pancreatic islets using a microfluidic device, Lab Chip, 16, 2921, 10.1039/C6LC00345A Ci, 2018, Vesicular stomatitis virus G protein transmembrane region is crucial for the hemi-fusion to full fusion transition, Sci. Rep., 8, 10669, 10.1038/s41598-018-28868-y Srivastava, 1991, Human immunodeficiency virus type 1 NL4-3 replication in four T-cell lines: rate and efficiency of entry, a major determinant of permissiveness, J. Virol., 65, 3900, 10.1128/jvi.65.7.3900-3902.1991