Evaluation The Role of CD33+ CD11b+ myeloid-derived Suppressor Cells in Patients With AML

Acute myeloid leukemia is a genetically heterogeneous clonal disease defined by the accumulation of immature cells in bone marrow and blood. The aim of this study is to evaluate the CD33, CD11b, and HLA-DR expression in Iraqi AML patients and its role in evasion of malignant cells from the immune sy...

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Main Authors: Hala Hamad, Zeyad Shabeeb, Muthanna Awad
פורמט: Article
שפה:English
יצא לאור: University of Anbar 2022-07-01
סדרה:مجلة جامعة الانبار للعلوم الصرفة
נושאים:
גישה מקוונת:https://juaps.uoanbar.edu.iq/article_174817_143e205f7cef772515ca84516007c0cb.pdf
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author Hala Hamad
Zeyad Shabeeb
Muthanna Awad
author_facet Hala Hamad
Zeyad Shabeeb
Muthanna Awad
author_sort Hala Hamad
collection DOAJ
description Acute myeloid leukemia is a genetically heterogeneous clonal disease defined by the accumulation of immature cells in bone marrow and blood. The aim of this study is to evaluate the CD33, CD11b, and HLA-DR expression in Iraqi AML patients and its role in evasion of malignant cells from the immune system. This study was conducted on 60 patients with AML and 20 healthy individuals as a control group to evaluate the expression of CD33 and CD11b using flow-cytometry in peripheral blood, and evaluate Interferons-γ (IFN-γ) and Transforming Growth Factor-β1 (TGF-β1) levels. A statistically non-significant difference (P < 0.005) between the AML patients and control group with regard to the expression of CD33, CD11b, and HLA-DR was observed. Analysis of CD33 expression in myeloid-derived suppressor cells (MDSCs) showed a significant decrease in the proportion of CD33 positive MDSC cells in isolated peripheral blood samples (88.078 ± 1.284). Also, the expression of CD11b in MDSC cells was high (98.841±1.935) in MDSC cells. The mean level of IFN-γ (pg/ml) increased in AML in compared to control group (9.202 ± 0.244), (7.906±1.22), respectively. While TGF- β1 (pg/ml) concentration was found to be elevated in AML patients (69.04 ± 9.92) compared to control group (33.884 ± 2.888). In conclusion, circulating MDSCs were significantly elevated in peripheral blood of patients with AML and characterized by the CD33+CD11b + phenotype; TGF-β1 and IFN-γ can be released in the presence of native human AML cells and affect AML cell proliferation and evasion from immune system.
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spelling doaj.art-a7f96eac9f5b4fe6b75d52a7e8449b482023-12-28T22:01:15ZengUniversity of Anbarمجلة جامعة الانبار للعلوم الصرفة1991-89412706-67032022-07-011611810.37652/juaps.2022.174817174817Evaluation The Role of CD33+ CD11b+ myeloid-derived Suppressor Cells in Patients With AMLHala Hamad0Zeyad Shabeeb1Muthanna Awad2Department of Biology , Collage of Science , University Of Anbar , Anbar , IraqNational center of hematology , University Of Mustansiriyah, Baghdad , IraqDepartment of Biology , College of Education for Pure Sciences , University Of Anbar , Anbar , IraqAcute myeloid leukemia is a genetically heterogeneous clonal disease defined by the accumulation of immature cells in bone marrow and blood. The aim of this study is to evaluate the CD33, CD11b, and HLA-DR expression in Iraqi AML patients and its role in evasion of malignant cells from the immune system. This study was conducted on 60 patients with AML and 20 healthy individuals as a control group to evaluate the expression of CD33 and CD11b using flow-cytometry in peripheral blood, and evaluate Interferons-γ (IFN-γ) and Transforming Growth Factor-β1 (TGF-β1) levels. A statistically non-significant difference (P < 0.005) between the AML patients and control group with regard to the expression of CD33, CD11b, and HLA-DR was observed. Analysis of CD33 expression in myeloid-derived suppressor cells (MDSCs) showed a significant decrease in the proportion of CD33 positive MDSC cells in isolated peripheral blood samples (88.078 ± 1.284). Also, the expression of CD11b in MDSC cells was high (98.841±1.935) in MDSC cells. The mean level of IFN-γ (pg/ml) increased in AML in compared to control group (9.202 ± 0.244), (7.906±1.22), respectively. While TGF- β1 (pg/ml) concentration was found to be elevated in AML patients (69.04 ± 9.92) compared to control group (33.884 ± 2.888). In conclusion, circulating MDSCs were significantly elevated in peripheral blood of patients with AML and characterized by the CD33+CD11b + phenotype; TGF-β1 and IFN-γ can be released in the presence of native human AML cells and affect AML cell proliferation and evasion from immune system.https://juaps.uoanbar.edu.iq/article_174817_143e205f7cef772515ca84516007c0cb.pdfcd11bcd33hla-drmdscaml
spellingShingle Hala Hamad
Zeyad Shabeeb
Muthanna Awad
Evaluation The Role of CD33+ CD11b+ myeloid-derived Suppressor Cells in Patients With AML
مجلة جامعة الانبار للعلوم الصرفة
cd11b
cd33
hla-dr
mdsc
aml
title Evaluation The Role of CD33+ CD11b+ myeloid-derived Suppressor Cells in Patients With AML
title_full Evaluation The Role of CD33+ CD11b+ myeloid-derived Suppressor Cells in Patients With AML
title_fullStr Evaluation The Role of CD33+ CD11b+ myeloid-derived Suppressor Cells in Patients With AML
title_full_unstemmed Evaluation The Role of CD33+ CD11b+ myeloid-derived Suppressor Cells in Patients With AML
title_short Evaluation The Role of CD33+ CD11b+ myeloid-derived Suppressor Cells in Patients With AML
title_sort evaluation the role of cd33 cd11b myeloid derived suppressor cells in patients with aml
topic cd11b
cd33
hla-dr
mdsc
aml
url https://juaps.uoanbar.edu.iq/article_174817_143e205f7cef772515ca84516007c0cb.pdf
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