Author/Authors :
Saadati, Nayyereh Rheumatic Diseases Research Center - Mashhad University of Medical Sciences, Mashhad, Iran , khodashahi, Mandana Rheumatic Diseases Research Center - Mashhad University of Medical Sciences, Mashhad, Iran , Rezaieyazdi, Zahra Rheumatic Diseases Research Center - Mashhad University of Medical Sciences, Mashhad, Iran , Sahebari, Maryam Rheumatic Diseases Research Center - Mashhad University of Medical Sciences, Mashhad, Iran , Saremi, Zeinab Department of social medicine - Faculty of Medicine - Mashhad University of Medical Sciences, Mashhad, Iran , Haftcheshmeh, Mohammadian Department of Medical Immunology - Faculty of Medicine - Mashhad University of Medical Sciences, Mashhad, Iran , Rafatpanah, Houshang Immunology Research Center - School of Medicine - Mashhad University of Medical Sciences, Mash had, Iran , Salehi, Maryam Department of social medicine - Faculty of Medicine - Mashhad University of Medical Sciences, Mashhad, Iran
Abstract :
Rheumatoid arthritis (RA) is described as a systemic and chronic autoimmune disease characterized by inflammatory polyarthritis. Lymphocyte-activation gene 3 (LAG3) is a membrane glycoprotein expressed on activated, exhausted, and regulatory T cells. LAG3 plays a major role in the function of Treg cells. LAG3 also has a soluble form (sLAG3) with a controversial role. Objective: To evaluate the serum level of sLAG3 in rheumatoid arthritis patients in comparison with healthy subjects and assess its association with the disease activity. Methods: This cross-sectional study was performed on 105 patients with RA referred to Ghaem hospital of Mashhad, Iran. We divided the participants into four groups: 1) 35 untreated patients with newly diagnosed RA, 2) 35 active RA patients, 3) 35 patients in the remission phase of the disease, and 4) 35 healthy individuals matched in terms of age and sex. After completing the interview and questionnaire, the sLAG3 was evaluated by commercial ELISA. Results: The serum level of sLAG3 significantly increased in RA patients (76.78 ng/ml) as compared with the healthy participants (51.67, p=0.002). However, there was no significant difference between RA patients in the remission phase of the disease (114.11 ng/ml) and those with moderate to high disease activity (63.06 ng/ml, p=0.076). Conclusion: This study provided insights into the role of sLAG3 in the immunopathogenesis of RA disease, but further investigations are also warranted
Keywords :
Soluble sLAG3 , Rheumatoid Arthritis , Disease Activity , Regulatory T Cells