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An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Elevated soluble CD226 in Takayasu arteritis is useful for differentiation from giant cell arteritis, disease
Miki Nakano1, Masahiro Ayano1, Shoichi Fukui2
1Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Takayasu arteritis (TAK) is characterized by vascular injury, in which endothelial cells and immune cells including natural killer cells, have key roles. CD226 is an activating receptor expressed on natural killer cells and T cells, and the soluble form of CD226 (sCD226) is increased in diseases involving these cells. Therefore, we investigated the utility of serum sCD226 as a biomarker for TAK. Serum sCD226 levels were measured using an enzyme-linked immunosorbent assay in 34 TAK patients and 21 giant cell arteritis (GCA) patients. The associations between sCD226 levels and the angiographic classification, disease activity, and prognosis of TAK were analyzed. Serum sCD226 levels were significantly higher in TAK patients than in GCA patients. In patients with TAK, serum sCD226 levels were significantly elevated in the group of type Ⅴ compared with type Ⅰ to Ⅳ. Serum sCD226 levels were also elevated in patients with active TAK and in those with poor responses to corticosteroids. Moreover, the cumulative probability of relapse was increased in patients with high sCD226 levels. Serum sCD226 levels differentiated TAK from GCA and were associated with disease activity and relapse of TAK. Thus, serum sCD226 might be a useful biomarker for the management of TAK.
Takayasu arteritis (TAK) is characterized by vascular injury, in which endothelial cells and immune cells including natural killer cells, have key roles. CD226 is an activating receptor expressed on natural killer cells and T cells, and the soluble form of CD226 (sCD226) is increased in diseases involving these cells. Therefore, we investigated the utility of serum sCD226 as a biomarker for TAK. Serum sCD226 levels were measured using an enzyme-linked immunosorbent assay in 34 TAK patients and 21 giant cell arteritis (GCA) patients. The associations between sCD226 levels and the angiographic classification, disease activity, and prognosis of TAK were analyzed. Serum sCD226 levels were significantly higher in TAK patients than in GCA patients. In patients with TAK, serum sCD226 levels were significantly elevated in the group of type Ⅴ compared with type Ⅰ to Ⅳ. Serum sCD226 levels were also elevated in patients with active TAK and in those with poor responses to corticosteroids. Moreover, the cumulative probability of relapse was increased in patients with high sCD226 levels. Serum sCD226 levels differentiated TAK from GCA and were associated with disease activity and relapse of TAK. Thus, serum sCD226 might be a useful biomarker for the management of TAK.
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