Publications
Polychromatic flow cytometry in the clinical laboratory
Abstract
SUMMARY: Technological advances in flow cytometry include increasingly sophisticated instruments and an expanding range of fluorochromes. These advances are making it possible to detect an increasing number of markers on a single cell. The term polychromatic flow cytometry applies to such systems that detect five or more markers simultaneously. This review provides an overview of the current and future impact of polychromatic flow cytometry in the clinical laboratory. The use of multiple markers has several advantages in the diagnosis and monitoring of haematological malignancies. Cell populations can be analysed more comprehensively and efficiently, and abnormal populations can be distinguished more readily when normal counterparts are present. Polychromatic flow cytometry is particularly useful in the evaluation of plasma cells, and the role of flow cytometry in the assessment of plasma cell disorders is reviewed in depth. There is improved sensitivity in the assessment of small populations, which is critical in the evaluation of minimal residual disease. Flow cytometry can also play a role in assessment of circulating tumour cells in carcinoma. Introduction of polychromatic flow cytometry is a complex process with many challenges including design of antibody panels and instrument compensation. Developments in data analysis are required to realise the full benefits of the other technical advances. Standardisation of protocols may reduce inter-laboratory variation. While the complexity of polychromatic flow cytometry creates challenges, it has substantial potential to improve clinical analysis.
Type | Journal |
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Authors | Sewell, W. A.; Smith, S. A. |
Responsible Garvan Author | Professor Bill Sewell |
Publisher Name | PATHOLOGY |
Published Date | 2011-09-02 |
Published Volume | 43 |
Published Issue | 6 |
Published Pages | 580-91 |
Status | Published in-print |
DOI | 10.1097/PAT.0b013e32834a69ae |
URL link to publisher's version | http://www.ncbi.nlm.nih.gov/pubmed/21881537 |
OpenAccess link to author's accepted manuscript version | https://publications.gimr.garvan.org.au/open-access/11173 |