Frequency of regulatory B cells phenotypes in breast cancer patients in Egypt |
The Egyptian Journal of Immunology Volume 28 (1), January, 2021 Pages: 12–22. www.Ejimmunology.org https://doi.org/10.55133/eji.280102 |
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Sherein G Elgendy1, Ehsan MW El-Sabaa2, Shabaan H Ahmed1, Samir SM Eid3 and Mohamed A El-Feky1 |
1Department of Medical Microbiology & Immunology, Faculty of Medicine, Assiut University, Assiut, Egypt.
2Department of Microbiology & Immunology, Faculty of Pharmacy, Assiut University, Assiut, Egypt. 3Department of Clinical Oncology & Nuclear Medicine, Faculty of Medicine, Assiut University, Assiut, Egypt. |
Corresponding author: Sherein G. Elgendy, Department of Medical Microbiology & Immunology, Faculty of Medicine, Assiut, University, Egypt. E-mail: Shereinelgendy@yahoo.com |
Abstract
Accumulating evidence has indicated that immune regulatory cells are involved in the establishment of the anti-tumor activity, however; the role of regulatory B cells (B-regs) in breast cancer (BC) remains unclear. This study intended to assess the frequency of peripheral B-regs phenotypes in patients with BC, and to determine the relation between these phenotypes and the patient’s clinicopathological characters. The expressions of the immune cell populations were analyzed by four-color flow cytometry in 40 naïve BC patients and 10 age-matched apparently healthy individuals as controls attending the department of Clinical Oncology and Nuclear Medicine at Assiut University Hospitals. The percentages of B-regs phenotypes CD19+IL10+ and CD19+CD24hiCD27+IL10+ were higher in BC patients than in the controls. The percentage of CD19+IL10+ B cells phenotype was significantly associated with the HER-2 expression levels, T, and N stages of BC. In conclusion, high percentage of B-regs phenotypes CD19+IL10+ and CD19+CD24hiCD27+IL10+ in BC patients indicates a possible role in immune suppression during the development of BC.
Keywords: Breast cancer; Clinicopathological characteristics; regulatory B cell; interleukin-10.
Date received: 23 January 2021; accepted: 22 April 2021
PMID: 34147050
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