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Flow cytometric signature of CD371-positive B-cell acute lymphoblastic leukemia

OBJECTIVES: Multiparametric flow cytometry (MFC) aids in the diagnosis and management of B-cell acute lymphoblastic leukemia (B-ALL) by establishing a baseline immunophenotype for leukemic cells and measuring minimal residual disease (MRD) throughout the course of treatment. Aberrant expression patt...

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Autores principales: Shakah, Hind, Tbakhi, Abdelghani, Khudirat, Saleh, Abweh, Ruba Al, Hasasna, Nabil, Alwhaidi, Alaa, Khoujah, Abdallah, Barakat, Fareed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566281/
https://www.ncbi.nlm.nih.gov/pubmed/37818740
http://dx.doi.org/10.1177/03000605231203842
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author Shakah, Hind
Tbakhi, Abdelghani
Khudirat, Saleh
Abweh, Ruba Al
Hasasna, Nabil
Alwhaidi, Alaa
Khoujah, Abdallah
Barakat, Fareed
author_facet Shakah, Hind
Tbakhi, Abdelghani
Khudirat, Saleh
Abweh, Ruba Al
Hasasna, Nabil
Alwhaidi, Alaa
Khoujah, Abdallah
Barakat, Fareed
author_sort Shakah, Hind
collection PubMed
description OBJECTIVES: Multiparametric flow cytometry (MFC) aids in the diagnosis and management of B-cell acute lymphoblastic leukemia (B-ALL) by establishing a baseline immunophenotype for leukemic cells and measuring minimal residual disease (MRD) throughout the course of treatment. Aberrant expression patterns of myeloid markers in B-ALL are also examined during long-term surveillance. Here, we investigated the utility of the newly described myeloid marker cluster of differentiation (CD)371 in MRD surveillance via MFC in patients with CD371-positive B-ALL. METHODS: Eight-color MFC with standard panels (including CD371) was used to evaluate 238 patients with newly diagnosed B-ALL. Expression levels of key markers were retrospectively assessed at diagnosis, as well as days 15 and 33 of therapy. RESULTS: CD371 was expressed in 8.4% of patients with B-ALL. CD371 positivity was associated with older age at diagnosis, higher expression levels of CD34 and CD38, and lower expression levels of CD10 and CD20. Residual leukemic cells demonstrated decreased CD10 expression and increased CD45 expression after therapy, whereas CD371 expression remained stable. CONCLUSIONS: Patients with CD371-positive B-ALL exhibit a specific signature that merits further analysis, particularly because it has been associated with DUX4 rearrangement.
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spelling pubmed-105662812023-10-12 Flow cytometric signature of CD371-positive B-cell acute lymphoblastic leukemia Shakah, Hind Tbakhi, Abdelghani Khudirat, Saleh Abweh, Ruba Al Hasasna, Nabil Alwhaidi, Alaa Khoujah, Abdallah Barakat, Fareed J Int Med Res Retrospective Clinical Research Report OBJECTIVES: Multiparametric flow cytometry (MFC) aids in the diagnosis and management of B-cell acute lymphoblastic leukemia (B-ALL) by establishing a baseline immunophenotype for leukemic cells and measuring minimal residual disease (MRD) throughout the course of treatment. Aberrant expression patterns of myeloid markers in B-ALL are also examined during long-term surveillance. Here, we investigated the utility of the newly described myeloid marker cluster of differentiation (CD)371 in MRD surveillance via MFC in patients with CD371-positive B-ALL. METHODS: Eight-color MFC with standard panels (including CD371) was used to evaluate 238 patients with newly diagnosed B-ALL. Expression levels of key markers were retrospectively assessed at diagnosis, as well as days 15 and 33 of therapy. RESULTS: CD371 was expressed in 8.4% of patients with B-ALL. CD371 positivity was associated with older age at diagnosis, higher expression levels of CD34 and CD38, and lower expression levels of CD10 and CD20. Residual leukemic cells demonstrated decreased CD10 expression and increased CD45 expression after therapy, whereas CD371 expression remained stable. CONCLUSIONS: Patients with CD371-positive B-ALL exhibit a specific signature that merits further analysis, particularly because it has been associated with DUX4 rearrangement. SAGE Publications 2023-10-11 /pmc/articles/PMC10566281/ /pubmed/37818740 http://dx.doi.org/10.1177/03000605231203842 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Retrospective Clinical Research Report
Shakah, Hind
Tbakhi, Abdelghani
Khudirat, Saleh
Abweh, Ruba Al
Hasasna, Nabil
Alwhaidi, Alaa
Khoujah, Abdallah
Barakat, Fareed
Flow cytometric signature of CD371-positive B-cell acute lymphoblastic leukemia
title Flow cytometric signature of CD371-positive B-cell acute lymphoblastic leukemia
title_full Flow cytometric signature of CD371-positive B-cell acute lymphoblastic leukemia
title_fullStr Flow cytometric signature of CD371-positive B-cell acute lymphoblastic leukemia
title_full_unstemmed Flow cytometric signature of CD371-positive B-cell acute lymphoblastic leukemia
title_short Flow cytometric signature of CD371-positive B-cell acute lymphoblastic leukemia
title_sort flow cytometric signature of cd371-positive b-cell acute lymphoblastic leukemia
topic Retrospective Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566281/
https://www.ncbi.nlm.nih.gov/pubmed/37818740
http://dx.doi.org/10.1177/03000605231203842
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