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Validation of the single-platform ISHAGE protocol for enumeration of CD34+ hematopoietic stem cells in umbilical cord blood in a Brazilian center

BACKGROUND: This study aims to validate the single-platform method for enumeration of CD34+ cells, by comparing the performance of two different commercial kits, as well as to evaluate the efficiency of the Accuri(TM) C6 cytometer in providing direct counts of absolute cell numbers. METHOD: We evalu...

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Detalles Bibliográficos
Autores principales: Pedrosa de Lira de Morais, Carla Cristina, Dias Alves Pinto, Juliana, Wagner de Souza, Karen, Izu, Marina, Fernando da Silva Bouzas, Luis, Henrique Paraguassú-Braga, Flávio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Hematologia e Hemoterapia 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885393/
https://www.ncbi.nlm.nih.gov/pubmed/33358615
http://dx.doi.org/10.1016/j.htct.2020.09.151
Descripción
Sumario:BACKGROUND: This study aims to validate the single-platform method for enumeration of CD34+ cells, by comparing the performance of two different commercial kits, as well as to evaluate the efficiency of the Accuri(TM) C6 cytometer in providing direct counts of absolute cell numbers. METHOD: We evaluated 20 samples from umbilical cord blood (UCB), comparing the two different methodologies for enumeration of CD34+ cells: single and dual-platform. For the assessment of the single-platform, Procount and SCE kits were used, both of which use fluorescent beads as a counting reference to obtain absolute CD34+ cells numbers. Moreover, after the acquisition of samples in flow cytometer Accuri(TM) C6, following the protocol established for each kit, the number of CD34+ cells was recalculated, considering the cell count provided by the Accuri(TM) C6. MAIN RESULTS: In our analysis, the results showed a strong correlation between the number of CD34+ cells/μL (r(2) = 0.77) when comparing the SCE kit and the current dual-platform method. On the other hand, the comparison between Procount kit and dual-platform results showed a moderate correlation for the number of CD34+/μL cells (r(2) = 0.64). CONCLUSION: Our results showed that the Accuri(TM) C6 flow cytometer can be used safely, applying both the dual and single platform analysis strategy. Considering the ISHAGE protocol-based single-platform approach, as the most appropriate methodology for CD34+ cells enumeration, our results demonstrated that the SCE kit has great potential for national standardization of UCB samples analysis methodology.