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Expression of Galectin-9 and correlation with disease activity and vascular endothelial growth factor in rheumatoid arthritis
Y. Wang1, L. Song2, J. Sun3, Y. Sui4, D. Li5, G. Li6, J. Liu7, Q. Shu8
- Department of Rheumatology and Immunology, Guangdong Second Provincial General Hospital, Guangzhou, Guangdong, and Department of Rheumatology, Qilu Hospital of Shandong University, Ji’nan, Shandong, China.
- Department of Rheumatology, Qilu Hospital of Shandong University, Ji’nan, Shandong, and Shenzhen Research Institute of Shandong University, Shenzhen, Guangdong, China.
- Department of Rheumatology, Qilu Hospital of Shandong University, Ji’nan, Shandong, and Department of Nephrology and Immunology, Shandong Provincial Third Hospital, Ji’nan, Shandong, China.
- Department of Rheumatology, Qilu Hospital of Shandong University, Ji’nan, Shandong, and Department of Rheumatology and Immunology, Yantai Mountain Hospital, Yantai, Shandong, China.
- Shenzhen Research Institute of Shandong University, Shenzhen, Guangdong, and Cryomedicine Laboratory, Qilu Hospital of Shandong University, Ji’nan, Shandong, China.
- Shenzhen Research Institute of Shandong University, Shenzhen, Guangdong, and Department of Haematology, Qilu Hospital of Shandong University, Ji’nan, Shandong, China.
- Department of Rheumatology, Qilu Hospital of Shandong University, Ji’nan, Shandong, China.
- Department of Rheumatology, Qilu Hospital of Shandong University, Ji’nan, Shandong, and Shenzhen Research Institute of Shandong University, Shenzhen, Guangdong, China. shuqiang@sdu.edu.cn
CER12315
2020 Vol.38, N°4
PI 0654, PF 0661
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PMID: 31820713 [PubMed]
Received: 10/04/2019
Accepted : 02/09/2019
In Press: 16/11/2019
Published: 28/07/2020
Abstract
OBJECTIVES:
Despite the important role of Galectin-9 (Gal-9) in inflammation and angiogenesis, only a few studies on Galectin-9 expression have been performed in rheumatoid arthritis (RA) patients. The present study aimed to identify the concentration of Galectin-9 in plasma, its expression in peripheral blood T cell subsets in RA patients, and the association between Galectin-9 and vascular endothelial growth factor (VEGF) in RA.
METHODS:
One hundred and five active RA patients and 52 age- and sex-matched healthy controls (HCs) were enrolled in the study. Gal-9, vascular endothelial growth factor (VEGF), and tumour necrosis factor (TNF)-α level in plasma were determined by ELISA. The intracellular positive expression rates and medium fluorescence intensity (MFI) of Gal-9 and VEGF in T cell subsets, were examined by flow cytometry.
RESULTS:
Plasma Gal-9, TNF-α, and VEGF levels were higher in the RA group than in the HCs group. The plasma Gal-9 level positively correlated with Gal-9 expression in the total lymphocyte and CD3+ T cell, CRP, SDAI, and CDAI of RA patients. The Gal-9 expressions in the cytoplasm of CD4+ T, CD8+ T, Treg, and DNT cells positively correlated with plasma TNF-α levels in RA patients. The Gal-9 expressions in CD4+ T and CD8+ T subsets also positively correlated with plasma VEGF levels. The plasma VEGF levels and VEGF expressions in CD4+ T, CD8+ T, and Treg subsets positively correlated with SDAI and CRP in RA patients.
CONCLUSIONS:
Gal-9 can be a potential biomarker for RA disease activity. Gal-9 is probably associated with angiogenesis processing in RA.