The Involvement of LAG-3positive Plasma Cells in the Development of Multiple Myeloma

流式细胞术 浆细胞失调 CD8型 不确定意义的单克隆抗体病 多发性骨髓瘤 生物 免疫学 分子生物学 化学 癌症研究 免疫系统 单克隆 单克隆抗体 抗体 免疫球蛋白轻链
作者
Natalia Kreiniz,Nasren Eiza,Tamar Tadmor,Ilana Levy Yurkovski,Sarah Matarasso Greenfeld,Adi D. Sabag,Raeda Mubariki,Celia Suriu,Ekaterina Votinov,Elias Toubi,Zahava Vadasz
出处
期刊:International Journal of Molecular Sciences [MDPI AG]
卷期号:25 (1): 549-549
标识
DOI:10.3390/ijms25010549
摘要

The Lymphocyte-Activation Protein 3 (LAG-3) inhibitory receptor is expressed on regulatory plasma cells (PCs). Micro-environmental cells that express LAG-3 were found to be increased during the progression of smoldering multiple myeloma (SMM). To assess the possible role of LAG-3 expression on regulatory PCs in patients with plasma cell dyscrasia. Purified Cluster of Differentiation 138 (CD138+) PCs from patients with premalignant conditions, active multiple myeloma (MM), and controls were analyzed for the expression of LAG-3 by flow cytometry. Autologous CD8+T cells were incubated with sorted LAG-3pos or LAG-3neg PCs for 24 h. The expression of granzyme (Grz) in CD8+T cells was assessed by flow cytometry. LAG-3 expression on PCs in active MM (newly diagnosed and relapse refractory MM) was significantly increased compared to monoclonal gammopathy of undetermined significance (MGUS)/ SMM. Grz expression was significantly decreased in CD8+T cells incubated with CD138+LAG-3pos PCs, compared to CD138+LAG-3neg PCs in patients with plasma cell dyscrasia, n = 31, p = 0.0041. LAG-3 expression on malignant PCs can be involved in the development of MM from MGUS by decreasing the expression of Grz in CD8+T cells.
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