Immune monitoring using mass cytometry and related high-dimensional imaging approaches

被引:118
|
作者
Hartmann, Felix J. [1 ]
Bendall, Sean C. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Palo Alto, CA 94304 USA
基金
瑞士国家科学基金会;
关键词
SINGLE-CELL ANALYSIS; FLOW-CYTOMETRY; B-CELLS; SUBCELLULAR RESOLUTION; T-CELLS; REVEALS; SIGNATURE; DISEASE; IDENTIFICATION; PROGRESSION;
D O I
10.1038/s41584-019-0338-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The cellular complexity and functional diversity of the human immune system necessitate the use of high-dimensional single-cell tools to uncover its role in multifaceted diseases such as rheumatic diseases, as well as other autoimmune and inflammatory disorders. Proteomic technologies that use elemental (heavy metal) reporter ions, such as mass cytometry (also known as CyTOF) and analogous high-dimensional imaging approaches (including multiplexed ion beam imaging (MIBI) and imaging mass cytometry (IMC)), have been developed from their low-dimensional counterparts, flow cytometry and immunohistochemistry, to meet this need. A growing number of studies have been published that use these technologies to identify functional biomarkers and therapeutic targets in rheumatic diseases, but the full potential of their application to rheumatic disease research has yet to be fulfilled. This Review introduces the underlying technologies for high-dimensional immune monitoring and discusses aspects necessary for their successful implementation, including study design principles, analytical tools and future developments for the field of rheumatology. Single-cell proteomic techniques that use elemental (heavy metal) reporter ions increase the number of parameters that can be studied at once in whole tissues. This Review discusses the practical aspects of using such technologies in rheumatic disease research.
引用
收藏
页码:87 / 99
页数:13
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