细胞毒性T细胞
抗原
CD8型
T细胞受体
单元格排序
T细胞
生物
分子生物学
下调和上调
抗原提呈细胞
表位
链霉菌
CD3型
细胞生物学
免疫学
白细胞介素21
流式细胞术
免疫系统
生物化学
体外
基因
作者
Miaojuan Huang,Jian Zhang,Weisan Chen
标识
DOI:10.1016/j.jim.2019.06.013
摘要
As T cell activation leads to downregulation of T cell receptor (TCR) and coreceptor CD8, we developed a novel FACS-based sorting method to enrich activated antigen-specific CD8+ T cells. Using multiple established or low percentage T cell cultures, with either single antigen specificity or multiple influenza A virus antigen specificities, we have optimized the sorting method for T cell activation time and stimulating antigen dose. We have also sorted various numbers of antigen-specific CD8+ T cells into 96-well plates to demonstrate these T cells are capable of expanding into nearly pure CD8+ T cell lines. Our approach has the advantage of sorting antigen-specific T cells without knowing their specific antigenic epitopes or restricting HLA. We believe this method can be very helpful for successfully establishing CD8+ T cell lines for various purpose, including immunotherapy.
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