4.5 Review

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

期刊

NATURE REVIEWS RHEUMATOLOGY
卷 16, 期 2, 页码 87-99

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NATURE PORTFOLIO
DOI: 10.1038/s41584-019-0338-z

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资金

  1. EMBO organization [ALTF 1141-2017]
  2. Novartis Foundation for Medical-Biological Research [16C148]
  3. Swiss National Science Foundation (SNF Early Postdoc Mobility) [P2ZHP3-171741]
  4. Damon Runyon Cancer Research Foundation Fellowship [DRG-2017-09]
  5. NIH [1DP2OD022550-01, 1R01AG056287-01, 1R01AG057915-01, 1-R00-GM104148-01, 1U24CA224309-01, 5U19AI116484-02, U19 AI104209]
  6. Stanford Cancer Institute
  7. Swiss National Science Foundation (SNF) [P2ZHP3_171741] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

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.

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