OMIP‐109: 45‐color full spectrum flow cytometry panel for deep immunophenotyping of the major lineages present in human peripheral blood mononuclear cells with emphasis on the T cell memory compartment

免疫分型 流式细胞术 细胞仪 免疫学 CD8型 T细胞 外周血单个核细胞 生物 背景(考古学) 免疫系统 计算生物学 遗传学 古生物学 体外
作者
Lily M. Park,Joanne Lannigan,Quentin Low,María C. Jaimes,Diana L. Bonilla
出处
期刊:Cytometry Part A [Wiley]
卷期号:105 (11): 807-815 被引量:8
标识
DOI:10.1002/cyto.a.24900
摘要

Abstract The need for more in‐depth exploration of the human immune system has moved the flow cytometry field forward with advances in instrumentation, reagent development and availability, and user‐friendly implementation of data analysis methods. We developed a high‐quality human 45‐color panel, for comprehensive characterization of major cell lineages present in circulation including T cells, γδ T cells, NKT‐like cells, B cells, NK cells, monocytes, basophils, dendritic cells, and ILCs. Assay optimization steps are described in detail to ensure that each marker in the panel was optimally resolved. In addition, we highlight the outstanding discernment of cell activation, exhaustion, memory, and differentiation states of CD4+ and CD8+ T cells using this 45‐color panel. The panel enabled an in‐depth description of very distinct phenotypes associated with the complexity of the T cell memory response. Furthermore, we present how this panel can be effectively used for cell sorting on instruments with a similar optical layout to achieve the same level of resolution. Functional evaluation of sorted specific rare cell subsets demonstrated significantly different patterns of immunological responses to stimulation, supporting functional and phenotypic differences within the T cell memory subsets. In summary, the combination of full spectrum profiling technology and careful assay design and optimization results in a high resolution multiparametric 45‐color assay. This panel offers the opportunity to fully characterize immunological profiles present in peripheral blood in the context of infectious diseases, autoimmunity, neurodegeneration, immunotherapy, and biomarker discovery.
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