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Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes

Background and Aim. We studied through flow cytometry the expression of CD146 on different T cells, and B-cell ALL blasts trying to correlate its expression with different prognostic factors of B-cell ALL and treatment outcomes. Patients and Methods. All pediatric patients with B-cell ALL were subje...

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Autores principales: Zahran, Asmaa M., El-Badawy, Omnia, Elsayh, Khalid I., Mohamed, Wael M. Y., Riad, Khalid F., Abdel-Rahim, Mona H., Rayan, Amal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031726/
https://www.ncbi.nlm.nih.gov/pubmed/32090132
http://dx.doi.org/10.1155/2020/9736159
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author Zahran, Asmaa M.
El-Badawy, Omnia
Elsayh, Khalid I.
Mohamed, Wael M. Y.
Riad, Khalid F.
Abdel-Rahim, Mona H.
Rayan, Amal
author_facet Zahran, Asmaa M.
El-Badawy, Omnia
Elsayh, Khalid I.
Mohamed, Wael M. Y.
Riad, Khalid F.
Abdel-Rahim, Mona H.
Rayan, Amal
author_sort Zahran, Asmaa M.
collection PubMed
description Background and Aim. We studied through flow cytometry the expression of CD146 on different T cells, and B-cell ALL blasts trying to correlate its expression with different prognostic factors of B-cell ALL and treatment outcomes. Patients and Methods. All pediatric patients with B-cell ALL were subjected to bone marrow examination and cytochemistry, flow cytometric immunophenotyping using monoclonal antibodies utilized for diagnosis of B-ALL including CD34, CD19, CD10, CD22, and intracellular IgM. The diagnosis was based on standard morphologic, cytochemical, and immunophenotypic followed by flow cytometric detection of CD146 expression on blast cells, CD4(+), and CD8(+) T cells. RESULTS: Significant accumulations of CD146(+)CD4(+) cells, CD146(+)CD8(+) cells, CD4(+), CD8(+), and lymphocytes in patients were compared to controls, the mean percentages of CD146(+)CD4(+) cells, CD146(+)CD8(+) cells, and CD146(+) blasts were significantly higher in patients than controls, and in addition, these cells were associated with poor overall survival and disease-free survival. The median OS for patients with complete response was 22 ± 1.633 (95%CI = 18.799‐25.201), while for those without complete response, it was 13 ± 3.928 (95%CI = 5.301‐25.699), with log‐rank = 5.71, P = 0.017. CONCLUSION: CD146 was expressed significantly in children's B-ALL and associated with poor prognostic features including poor response and treatment outcomes and could be a possible poor prognostic factor in pediatric B-cell ALL.
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spelling pubmed-70317262020-02-21 Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes Zahran, Asmaa M. El-Badawy, Omnia Elsayh, Khalid I. Mohamed, Wael M. Y. Riad, Khalid F. Abdel-Rahim, Mona H. Rayan, Amal J Immunol Res Research Article Background and Aim. We studied through flow cytometry the expression of CD146 on different T cells, and B-cell ALL blasts trying to correlate its expression with different prognostic factors of B-cell ALL and treatment outcomes. Patients and Methods. All pediatric patients with B-cell ALL were subjected to bone marrow examination and cytochemistry, flow cytometric immunophenotyping using monoclonal antibodies utilized for diagnosis of B-ALL including CD34, CD19, CD10, CD22, and intracellular IgM. The diagnosis was based on standard morphologic, cytochemical, and immunophenotypic followed by flow cytometric detection of CD146 expression on blast cells, CD4(+), and CD8(+) T cells. RESULTS: Significant accumulations of CD146(+)CD4(+) cells, CD146(+)CD8(+) cells, CD4(+), CD8(+), and lymphocytes in patients were compared to controls, the mean percentages of CD146(+)CD4(+) cells, CD146(+)CD8(+) cells, and CD146(+) blasts were significantly higher in patients than controls, and in addition, these cells were associated with poor overall survival and disease-free survival. The median OS for patients with complete response was 22 ± 1.633 (95%CI = 18.799‐25.201), while for those without complete response, it was 13 ± 3.928 (95%CI = 5.301‐25.699), with log‐rank = 5.71, P = 0.017. CONCLUSION: CD146 was expressed significantly in children's B-ALL and associated with poor prognostic features including poor response and treatment outcomes and could be a possible poor prognostic factor in pediatric B-cell ALL. Hindawi 2020-02-08 /pmc/articles/PMC7031726/ /pubmed/32090132 http://dx.doi.org/10.1155/2020/9736159 Text en Copyright © 2020 Asmaa M. Zahran et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zahran, Asmaa M.
El-Badawy, Omnia
Elsayh, Khalid I.
Mohamed, Wael M. Y.
Riad, Khalid F.
Abdel-Rahim, Mona H.
Rayan, Amal
Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes
title Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes
title_full Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes
title_fullStr Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes
title_full_unstemmed Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes
title_short Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes
title_sort upregulation of cd146 in pediatric b-cell acute lymphocytic leukemia and its implications on treatment outcomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031726/
https://www.ncbi.nlm.nih.gov/pubmed/32090132
http://dx.doi.org/10.1155/2020/9736159
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