Wang Song-Rong, Zhong Na, Zhang Xin-Mei, Zhao Zhi-Bin, Balderas Robert, Li Liang, Lian Zhe-Xiong
Department of General Surgery, Guangzhou Digestive Disease Center, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, 510180, China.
Chronic Disease Laboratory, Institutes for Life Sciences and School of Medicine, South China University of Technology, Guangzhou, Guangdong, 510006, China.
Cytometry A. 2021 Mar;99(3):273-277. doi: 10.1002/cyto.a.24272. Epub 2020 Dec 10.
Dissecting the functional diversity of T cells is critical in elucidating mechanisms and in developing therapies for various diseases. Here, we designed a 31-parameter (29-color) panel to enable the characterization of T-cell subsets and immunophenotyping of the human peripheral blood and lymph nodes using cell surface staining. In addition to adaptive T-cell markers, TCR Vα24-Jα18, TCR γδ, TCR Vɑ7.2, and CD161 were included to identify iNKT, γδ T, and MAIT cells, respectively, which are innate-like T cells. C-X-C chemokine receptors (CXCR3, CXCR4, CXCR5, CXCR6) and C-C motif chemokine receptors (CCR4, CCR6, CCR7) were included to enable the identification of Th cell subsets (Th1, Th2, Th17), Tfh cell subsets (Tfh1, Tfh2, Tfh17), and Th cells with specific homing capacities. Furthermore, in this panel, we also used markers for assessing cell differentiation (CD45RO, CD7), activation (CD57, CD95, HLA-DR) and the expression of some cosignaling molecules (PD-1, NKG2D, CD28). Particularly, CD69 and CD103 were included for the further analysis of tissue resident memory T (Trm) cells. This panel would enable the in-depth immunophenotyping of human T-cell subsets, and may be applied in the monitoring, prognosis, and mechanistic studies of various immune-related diseases.
剖析T细胞的功能多样性对于阐明各种疾病的发病机制和开发治疗方法至关重要。在此,我们设计了一个包含31个参数(29种颜色)的组合,通过细胞表面染色来实现对T细胞亚群的表征以及对人外周血和淋巴结进行免疫表型分析。除了适应性T细胞标志物外,还纳入了TCR Vα24-Jα18、TCR γδ、TCR Vɑ7.2和CD161,分别用于鉴定iNKT细胞、γδ T细胞和MAIT细胞,这些都是固有样T细胞。还纳入了C-X-C趋化因子受体(CXCR3、CXCR4、CXCR5、CXCR6)和C-C基序趋化因子受体(CCR4、CCR6、CCR7),以鉴定Th细胞亚群(Th1、Th2、Th17)、滤泡辅助性T细胞亚群(Tfh1、Tfh2、Tfh17)以及具有特定归巢能力的Th细胞。此外,在这个组合中,我们还使用了评估细胞分化(CD45RO、CD7)、激活(CD57、CD95、HLA-DR)以及一些共信号分子(PD-1、NKG2D、CD28)表达的标志物。特别地,纳入了CD69和CD103用于进一步分析组织驻留记忆T(Trm)细胞。这个组合将能够对人T细胞亚群进行深入的免疫表型分析,并可能应用于各种免疫相关疾病的监测、预后评估和机制研究。