دورية أكاديمية

Enhanced Expression of Anti-CD19 Chimeric Antigen Receptor in piggyBac Transposon-Engineered T Cells

التفاصيل البيبلوغرافية
العنوان: Enhanced Expression of Anti-CD19 Chimeric Antigen Receptor in piggyBac Transposon-Engineered T Cells
المؤلفون: Daisuke Morita, Nobuhiro Nishio, Shoji Saito, Miyuki Tanaka, Nozomu Kawashima, Yusuke Okuno, Satoshi Suzuki, Kazuyuki Matsuda, Yasuhiro Maeda, Matthew H. Wilson, Gianpietro Dotti, Cliona M. Rooney, Yoshiyuki Takahashi, Yozo Nakazawa
المصدر: Molecular Therapy: Methods & Clinical Development, Vol 8, Iss C, Pp 131-140 (2018)
بيانات النشر: Elsevier, 2018.
سنة النشر: 2018
المجموعة: LCC:Genetics
LCC:Cytology
مصطلحات موضوعية: chimeric antigen receptor, non-viral vector, piggyBac, transposon, virus-specific antigens, acute lymphoblastic leukemia, refractory, Genetics, QH426-470, Cytology, QH573-671
الوصف: Adoptive T cell therapy using chimeric antigen receptor (CAR)-modified T cells is a promising cancer immunotherapy. We previously developed a non-viral method of gene transfer into T cells using a piggyBac transposon system to improve the cost-effectiveness of CAR-T cell therapy. Here, we have further improved our technology by a novel culture strategy to increase the transfection efficiency and to reduce the time of T cell manufacturing. Using a CH2CH3-free CD19-specific CAR transposon vector and combining irradiated activated T cells (ATCs) as feeder cells and virus-specific T cell receptor (TCR) stimulation, we achieved 51.4% ± 14% CAR+ T cells and 2.8-fold expansion after 14 culture days. Expanded CD19.CAR-T cells maintained a significant fraction of CD45RA+CCR7+ T cells and demonstrated potent antitumor activity against CD19+ leukemic cells both in vitro and in vivo. Therefore, piggyBac-based gene transfer may provide an alternative to viral gene transfer for CAR-T cell therapy.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2329-0501
Relation: http://www.sciencedirect.com/science/article/pii/S2329050117301286; https://doaj.org/toc/2329-0501
DOI: 10.1016/j.omtm.2017.12.003
URL الوصول: https://doaj.org/article/b87077edcc27440da345a159cfeca963
رقم الأكسشن: edsdoj.b87077edcc27440da345a159cfeca963
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23290501
DOI:10.1016/j.omtm.2017.12.003