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How to make usage of the standardized EuroFlow 8-color protocols possible for instruments of different manufacturers

Autores: Nováková, M.; Glier, H.; Brdicková, N.; Vlková, M.; Santos, A. H.; Lima, M.; Roussel, M.; Flores-Montero, J.; Szczepanski, T.; Böttcher, S.; van der Velden, V. H. J.; Fernandez, P.; Mejstríková, E.; Burgos Rodríguez, Leire; Paiva, B.; van Dongen, J. J. M.; Orfao, A.; Kalina, T. (Autor de correspondencia)
ISSN: 0022-1759
Volumen: 475
Número: 112388
Fecha de publicación: 2019
A critical component of the EuroFlow standardization of leukemia/lymphoma immunophenotyping is instrument setup. Initially, the EuroFlow consortium developed a step-by-step standard operating protocol for instrument setup of >=8-color flow cytometers that were available in 2006, when the EuroFlow activities started. Currently, there are 14 instruments from 9 manufacturers capable of 3-laser excitation and >=8 color measurements. The specific adaptations required in the instrument set-up to enable them to acquire the standardized 8-color EuroFlow protocols are described here. Overall, all 14 instruments can be fitted with similar violet, blue and red lasers for simultaneous measurements of >=8 fluorescent dyes. Since individual instruments differ both on their dynamic range (scale) and emission filters, it is not accurate to simply recalculate the target values to different scale, but adjustment of PMT voltages to a given emission filter and fluorochrome, is essential. For this purpose, EuroFlow has developed an approach using Type IIB (spectrally matching) particles to set-up standardized and fully comparable fluorescence measurements, in instruments from different manufacturers, as demonstrated here for the FACSCanto II, and Navios and MACSQuant flow cytometers. Data acquired after such adjustment on any of the tested cytometry platforms could be fully superimposed and therefore analyzed together.