Lymphocyte activation gene-3 (LAG-3) is a CD4 homologue expressed on the surface of activated conventional T cells and regulatory T (Treg) cells. In conventional T cells, LAG-3 acts as an inhibitory receptor of T cell inflammation. However, the role of LAG-3 in Treg cells remains controversial. In this study, we investigated the effect of LAG-3 on Tregs in osteoarthritis (OA). We observed that the proportion of LAG-3-expressing cells in CD4+CD25+/high T cells and Foxp3+CD4+CD25+/high T cells were significantly upregulated in OA patients. The level of LAG-3-to-Foxp3 ratio was further increased in synovial fluid. Several aspects of Treg responses in LAG-3+ and LAG-3- Treg cells were then examined. First, LAG-3+ Treg cells demonstrated significantly lower proliferation than LAG-3- Treg cells. Second, the increase in interleukin (IL)-10 and transforming growth factor (TGF)-β expression was significantly lower in LAG-3+ Treg cells than that in LAG-3- Treg cells. Third, LAG-3+ Treg cells were less capable of inhibiting the proliferation of CD4+CD25- conventional T cells than LAG-3- Treg cells. This study suggests that Treg cells in OA may be enriched with a LAG-3-expressing population that exhibits functional impairment, which limits their capacity in suppressing inflammation.
Keywords: IL-10; LAG-3; osteoarthritis; regulatory T cell.