FACS isolation of low percentage human antigen-specific CD8+ T cells based on activation-induced CD3 and CD8 downregulation

被引:6
作者
Huang, Miaojuan [1 ]
Zhang, Jian [2 ]
Chen, Weisan [1 ]
机构
[1] La Trobe Univ, Sch Mol Sci, La Trobe Inst Mol Sci, Bundoora, Vic, Australia
[2] Southern Med Univ, Zhujiang Hosp, Dept Oncol, 253 Ind Ave, Guangzhou, Guangdong, Peoples R China
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
CD8(+) cell; CD3 and CD8 downregulation; MHC CLASS-I; INFLUENZA-A VIRUS; RECEPTOR/CD3; COMPLEX; TETRAMER BINDING; IDENTIFICATION; PROTEIN; TRANSDUCTION; CLONOTYPES; RESPONSES; AFFINITY;
D O I
10.1016/j.jim.2019.06.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:35 / 43
页数:9
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