Development of a 43 color panel for the characterization of conventional and unconventional T-cell subsets, B cells, NK cells, monocytes, dendritic cells, and innate lymphoid cells using spectral flow cytometry

被引:42
|
作者
Sahir, Fairooz [1 ]
Mateo, Jericha Miles [1 ]
Steinhoff, Martin [2 ,3 ,4 ,5 ,6 ,7 ]
Siveen, Kodappully Sivaraman [1 ]
机构
[1] Hamad Med Corp, Translat Res Inst, Acad Hlth Syst, Flow Cytometry Core Facil, Doha, Qatar
[2] Hamad Med Corp, Dept Dermatol & Venereol, Doha, Qatar
[3] Hamad Med Corp, Dermatol Inst, Doha, Qatar
[4] Hamad Med Corp, Translat Res Inst, Acad Hlth Syst, Doha, Qatar
[5] Weill Cornell Med Qatar, Dept Dermatol, Doha, Qatar
[6] Qatar Univ, Med Sch, Doha, Qatar
[7] Weill Cornell Med Coll, Dept Med, New York, NY USA
关键词
dendritic cells; innate lymphoid cells; immunophenotyping; spectral flow cytometry; unconventional T cells;
D O I
10.1002/cyto.a.24288
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Although many flow cytometers can analyze 30-50 parameters, it is still challenging to develop a 40+ color panel for the phenotyping of immune cells using fluorochrome conjugated antibodies due to limitations in the availability of spectrally unique fluorochromes that can be excited by the commonly used laser lines (UV, Violet, Blue, Green/Yellow-green, and Red). Spectral flowcytometry is capable of differentiating fluorochromes with significant overlap in the emission spectra, enabling the use of spectrally similar fluorochrome pairs such as Brilliant Blue 515 and FITC in a single panel. We have developed a 43 color panel to characterize most of the immune subsets within the peripheral immune system, including conventional T cells, unconventional T cells such as invariant natural killer T cells (iNKT), Gamma delta (gamma delta) T-cell subsets (TCR V delta 2, TCR V gamma 9) and mucosal-associated invariant T cells (MAIT), B-cell subsets, natural killer (NK) cells, plasmacytoid dendritic cells, dendritic cell subsets, hematopoietic progenitor cells, basophils, and innate lymphoid cell (ILC) subsets (CD117, CRTH2). The panel includes surface markers to analyze activation (CD38, HLA-DR, ICOS/CD278), differentiation (CD45RA, CD27, CD28, CD57), expression of cytokine and chemokine receptors (CD25, CD127, CCR10, CCR6, CCR4, CXCR3, CXCR5, CRTH2/CD294), and co-inhibitory molecules and exhaustion (PD-1, CD223/LAG-3, TIGIT), which enables a deep characterization of PBMCs from peripheral blood. Cells were analyzed on a 5-laser Cytek Aurora and data analysis was done using FlowJo. This panel can help to make a thorough interpretation of immune system, specifically when specimen quantity is low. The panel has not been completely optimized but would rather act as a guide toward the development of a workflow for optimized multicolor immunophenotyping panel.
引用
收藏
页码:404 / 410
页数:7
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