L. Tashireva, A. Kalinchuk, T. Gerashchenko, O. Savelyeva, V. Perelmuter
{"title":"Subpopulations of B lymphocytes in patients with breast cancer depending on the PD-L1 status","authors":"L. Tashireva, A. Kalinchuk, T. Gerashchenko, O. Savelyeva, V. Perelmuter","doi":"10.20538/1682-0363-2023-1-88-95","DOIUrl":null,"url":null,"abstract":"Aim. To study the association between the functional potency and degree of maturity of B lymphocytes and PD-L1 expression in breast cancer patients.Materials and methods. The study included 37 patients with the morphologically verified diagnosis of invasive breast cancer of no special type (IBC NST). The PD-L1 status was determined immunohistochemically using the Ventana SP142 assay (Roche, USA). Using the multiplex flow cytometry-based assay and high-throughput sequencing of the tumor microenvironment, subpopulations of B lymphocytes and their CD27 and PD1 expression profiles were determined, taking into account the PD-L1 status.Results. In the tumor microenvironment, regardless of the PD-L1 status, expression signatures of five lymphocyte subpopulations were determined. However, in PD-L1-positive patients, the levels of B lymphocytes and immunoglobulin class-switched B lymphocytes were higher compared with PD-L1-negative patients. Evaluation of the number of different B lymphocyte subpopulations by flow cytometry showed that PD-1-positive B lymphocytes predominated in the tumor microenvironment in PD-L1-positive patients, regardless of the degree of lymphocyte maturity.Conclusion. The results of the study showed predominance of mature committed B lymphocytes and memory B lymphocytes capable of synthesizing immunoglobulins of different classes and Th2 cytokines involved in type 2 immune response in PD-L-positive tumor microenvironment. It suggests that immunotherapy with PD-L1 inhibitors is highly likely to activate cells with protumor potential and can ultimately contribute to breast cancer progression.","PeriodicalId":256912,"journal":{"name":"Bulletin of Siberian Medicine","volume":"87 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Siberian Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20538/1682-0363-2023-1-88-95","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Aim. To study the association between the functional potency and degree of maturity of B lymphocytes and PD-L1 expression in breast cancer patients.Materials and methods. The study included 37 patients with the morphologically verified diagnosis of invasive breast cancer of no special type (IBC NST). The PD-L1 status was determined immunohistochemically using the Ventana SP142 assay (Roche, USA). Using the multiplex flow cytometry-based assay and high-throughput sequencing of the tumor microenvironment, subpopulations of B lymphocytes and their CD27 and PD1 expression profiles were determined, taking into account the PD-L1 status.Results. In the tumor microenvironment, regardless of the PD-L1 status, expression signatures of five lymphocyte subpopulations were determined. However, in PD-L1-positive patients, the levels of B lymphocytes and immunoglobulin class-switched B lymphocytes were higher compared with PD-L1-negative patients. Evaluation of the number of different B lymphocyte subpopulations by flow cytometry showed that PD-1-positive B lymphocytes predominated in the tumor microenvironment in PD-L1-positive patients, regardless of the degree of lymphocyte maturity.Conclusion. The results of the study showed predominance of mature committed B lymphocytes and memory B lymphocytes capable of synthesizing immunoglobulins of different classes and Th2 cytokines involved in type 2 immune response in PD-L-positive tumor microenvironment. It suggests that immunotherapy with PD-L1 inhibitors is highly likely to activate cells with protumor potential and can ultimately contribute to breast cancer progression.