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Comments on EuroFlow standard operating procedures for instrument setup and compensation for BD FACS Canto II, Navios and BD FACS Lyric instruments

H. Glier, M. Novakova, J. Te Marvelde, A. Bijkerk, D. Morf, D. Thurner, K. Rejlova, S. Lange, J. Finke, A. van der Sluijs-Gelling, L. Sedek, J. Flores-Montero, S. Böttcher, P. Fernandez, M. Ritgen, JJM. van Dongen, A. Orfao, VHJ. van der Velden,...

. 2019 ; 475 (-) : 112680. [pub] 20191023

Language English Country Netherlands

Document type Journal Article, Research Support, Non-U.S. Gov't

Persistent link   https://www.medvik.cz/link/bmc20023410

This commentary discusses particularities of application of the EuroFlow standardization of flow cytometric analyses on three different flow cytometers. The EuroFlow consortium developed a fully standardized approach for flow cytometric immunophenotyping of hematological malignancies and primary immunodeficiencies. Standardized instrument setup is an essential part of EuroFlow standardization. Initially, the EuroFlow Consortium developed and optimized a step-by-step standard operating procedure (SOP) to setup 8-color BD FACSCanto II flow cytometer (Canto), with the later inclusion of Navios (Beckman Coulter) and BD FACSLyric (Lyric). Those SOPs were developed to enable standardized and fully comparable fluorescence measurements in the three flow cytometers. In Canto and Navios, mean fluorescence intensity (MFI) of a reference peak of Rainbow beads calibration particles is used to set up photomultiplier (PMT) voltages for each detector channel in individual instruments to reach the same MFI across distinct instruments. In turn, a new feature of Lyric instruments allows to share collection of attributes that are used to place the positive population at the same position among instruments in the form of assays, as one of its components integrated in the Cytometer Setup and Tracking (CS&T) module. The EuroFlow Lyric assays thus allow for standardized acquisition of 8-color EuroFlow panels on Lyric without the need to setup the PMT voltages on the individual instruments manually. In summary, the standardized instrument setup developed by EuroFlow enables cross-platform inter- and intra-laboratory standardization of flow cytometric measurements. This commentary provides a perspective on the modifications of the standardized EuroFlow instrument setup of Canto, Navios and Lyric instruments that are described in detail in individual instrument-specfic SOPs available at the EuroFlow website.

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$a Comments on EuroFlow standard operating procedures for instrument setup and compensation for BD FACS Canto II, Navios and BD FACS Lyric instruments / $c H. Glier, M. Novakova, J. Te Marvelde, A. Bijkerk, D. Morf, D. Thurner, K. Rejlova, S. Lange, J. Finke, A. van der Sluijs-Gelling, L. Sedek, J. Flores-Montero, S. Böttcher, P. Fernandez, M. Ritgen, JJM. van Dongen, A. Orfao, VHJ. van der Velden, T. Kalina,
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$a This commentary discusses particularities of application of the EuroFlow standardization of flow cytometric analyses on three different flow cytometers. The EuroFlow consortium developed a fully standardized approach for flow cytometric immunophenotyping of hematological malignancies and primary immunodeficiencies. Standardized instrument setup is an essential part of EuroFlow standardization. Initially, the EuroFlow Consortium developed and optimized a step-by-step standard operating procedure (SOP) to setup 8-color BD FACSCanto II flow cytometer (Canto), with the later inclusion of Navios (Beckman Coulter) and BD FACSLyric (Lyric). Those SOPs were developed to enable standardized and fully comparable fluorescence measurements in the three flow cytometers. In Canto and Navios, mean fluorescence intensity (MFI) of a reference peak of Rainbow beads calibration particles is used to set up photomultiplier (PMT) voltages for each detector channel in individual instruments to reach the same MFI across distinct instruments. In turn, a new feature of Lyric instruments allows to share collection of attributes that are used to place the positive population at the same position among instruments in the form of assays, as one of its components integrated in the Cytometer Setup and Tracking (CS&T) module. The EuroFlow Lyric assays thus allow for standardized acquisition of 8-color EuroFlow panels on Lyric without the need to setup the PMT voltages on the individual instruments manually. In summary, the standardized instrument setup developed by EuroFlow enables cross-platform inter- and intra-laboratory standardization of flow cytometric measurements. This commentary provides a perspective on the modifications of the standardized EuroFlow instrument setup of Canto, Navios and Lyric instruments that are described in detail in individual instrument-specfic SOPs available at the EuroFlow website.
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$a Novakova, Michaela $u CLIP, Department of Paediatric Hematology and Oncology, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
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$a Te Marvelde, Jeroen $u Department of Immunology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
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$a Bijkerk, Andre $u Department of Immunology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
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$a Morf, Daniela $u FACS/Stem cell Laboratory, Kantonsspital Aarau, Aarau, Switzerland.
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$a Thurner, Daniel $u CLIP, Department of Paediatric Hematology and Oncology, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
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$a Rejlova, Katerina $u CLIP, Department of Paediatric Hematology and Oncology, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
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$a Lange, Sandra $u Department III of Internal Medicine, University Medical Center Rostock, Rostock, Germany.
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$a Finke, Judith $u Second Department of Medicine, University Hospital of Schleswig Holstein (UKSH), Campus Kiel, Kiel, Germany.
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$a van der Sluijs-Gelling, Alita $u Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, the Netherlands.
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$a Sedek, Lukasz $u Department of Microbiology and Immunology, Medical University of Silesia in Katowice, Zabrze, Poland.
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$a Flores-Montero, Juan $u Cancer Research Center (IBMCC-CSIC/USAL-IBSAL), Cytometry Service (NUCLEUS) and Department of Medicine, University of Salamanca, Salamanca, Spain, Centro de Investigación Biomédica en Red de Cáncer (CIBER-ONC), CB16/12/00400, Instituto de Salud Carlos III, Madrid, Spain.
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$a Böttcher, Sebastian, $d 1971- $u Department III of Internal Medicine, University Medical Center Rostock, Rostock, Germany. $7 xx0327357
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$a Fernandez, Paula $u FACS/Stem cell Laboratory, Kantonsspital Aarau, Aarau, Switzerland.
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$a Ritgen, Matthias $u Second Department of Medicine, University Hospital of Schleswig Holstein (UKSH), Campus Kiel, Kiel, Germany.
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$a van Dongen, Jacques J M $u Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: J.J.M.van_Dongen@lumc.nl.
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$a Orfao, Alberto $u Cancer Research Center (IBMCC-CSIC/USAL-IBSAL), Cytometry Service (NUCLEUS) and Department of Medicine, University of Salamanca, Salamanca, Spain, Centro de Investigación Biomédica en Red de Cáncer (CIBER-ONC), CB16/12/00400, Instituto de Salud Carlos III, Madrid, Spain.
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$a van der Velden, Vincent H J $u Department of Immunology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
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$a Kalina, Tomas $u CLIP, Department of Paediatric Hematology and Oncology, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic. Electronic address: tomas.kalina@lfmotol.cuni.cz.
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