Nine-color flow cytometry for accurate measurement of T cell subsets and cytokine responses. Part I

Panel design by an empiric approach

Bridget E. McLaughlin, Nicole Baumgarth, Martin Bigos, Mario Roederer, Stephen C. De Rosa, John D. Altman, Douglas F. Nixon, Janet Ottinger, Carol Oxford, Thomas G. Evans, David Asmuth

Research output: Contribution to journalArticle

49 Citations (Scopus)

Abstract

Polychromatic flow cytometry offers the unprecedented ability to investigate multiple antigens per cell. Unfortunately, unwanted spectral overlaps and compensation problems increase when more than four colors are used, but these problems can be minimized if staining combinations are chosen carefully. We used an empiric approach to design, test and identify six-color T cell immunophenotyping reagent panels that can be expanded to include three or more functional or other markers in the FITC, PE, and APC channels without significant spectral limitations. Thirty different six-color T cell surface antigen reagent panels were constructed to identify major T cell subsets and maturational subtypes as defined by CCR7 and CD45RA expression, while excluding monocytes, B and non-viable cells. Staining performance of each panel was compared on cryopreserved cells from a single healthy donor recorded on a multiparameter cell sorter. Ten of the thirty reagent panels offered reliable resolution of T cell major and maturational surface markers. Of these, two panels were selected that showed the least spectral overlap and resulting background increase in the FITC, PE, and APC channels. These channels were left unoccupied for inclusion of additional phenotypic or functional markers, such as cytokines. Careful reagent titration and testing of multiple candidate panels are necessary to ensure quality results in multiparametric measurements.

Original languageEnglish (US)
Pages (from-to)400-410
Number of pages11
JournalCytometry Part A
Volume73
Issue number5
DOIs
StatePublished - May 2008

Fingerprint

T-Lymphocyte Subsets
Flow Cytometry
Color
Cytokines
Fluorescein-5-isothiocyanate
T-Lymphocytes
Staining and Labeling
Immunophenotyping
Surface Antigens
Monocytes
Antigens

Keywords

  • Compensation
  • Fluorochrome conjugated antibody
  • Polychromatic flow cytometry
  • T cell immunophenotyping

ASJC Scopus subject areas

  • Hematology
  • Cell Biology
  • Pathology and Forensic Medicine
  • Biophysics
  • Endocrinology

Cite this

Nine-color flow cytometry for accurate measurement of T cell subsets and cytokine responses. Part I : Panel design by an empiric approach. / McLaughlin, Bridget E.; Baumgarth, Nicole; Bigos, Martin; Roederer, Mario; De Rosa, Stephen C.; Altman, John D.; Nixon, Douglas F.; Ottinger, Janet; Oxford, Carol; Evans, Thomas G.; Asmuth, David.

In: Cytometry Part A, Vol. 73, No. 5, 05.2008, p. 400-410.

Research output: Contribution to journalArticle

McLaughlin, BE, Baumgarth, N, Bigos, M, Roederer, M, De Rosa, SC, Altman, JD, Nixon, DF, Ottinger, J, Oxford, C, Evans, TG & Asmuth, D 2008, 'Nine-color flow cytometry for accurate measurement of T cell subsets and cytokine responses. Part I: Panel design by an empiric approach', Cytometry Part A, vol. 73, no. 5, pp. 400-410. https://doi.org/10.1002/cyto.a.20555
McLaughlin, Bridget E. ; Baumgarth, Nicole ; Bigos, Martin ; Roederer, Mario ; De Rosa, Stephen C. ; Altman, John D. ; Nixon, Douglas F. ; Ottinger, Janet ; Oxford, Carol ; Evans, Thomas G. ; Asmuth, David. / Nine-color flow cytometry for accurate measurement of T cell subsets and cytokine responses. Part I : Panel design by an empiric approach. In: Cytometry Part A. 2008 ; Vol. 73, No. 5. pp. 400-410.
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