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

Authors :
Kreiniz, Natalia
Eiza, Nasren
Tadmor, Tamar
Levy Yurkovski, Ilana
Matarasso Greenfeld, Sarah
Sabag, Adi
Mubariki, Raeda
Suriu, Celia
Votinov, Ekaterina
Toubi, Elias
Vadasz, Zahava
Source :
International Journal of Molecular Sciences; Jan2024, Vol. 25 Issue 1, p549, 12p
Publication Year :
2024

Abstract

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<superscript>+)</superscript> 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<superscript>+</superscript>T cells were incubated with sorted LAG-3<superscript>pos</superscript> or LAG-3<superscript>neg</superscript> PCs for 24 h. The expression of granzyme (Grz) in CD8<superscript>+</superscript>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<superscript>+</superscript>T cells incubated with CD138<superscript>+</superscript>LAG-3<superscript>pos</superscript> PCs, compared to CD138<superscript>+</superscript>LAG-3<superscript>neg</superscript> 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<superscript>+</superscript>T cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16616596
Volume :
25
Issue :
1
Database :
Complementary Index
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
174717307
Full Text :
https://doi.org/10.3390/ijms25010549