Hypermethylation of Smad7 in CD4 + T cells is associated with the disease activity of rheumatoid arthritis

• Published in: Frontiers in immunology 2023-02, Vol.14, p.1104881-1104881
• Main Authors: Hu, Yiping, Xu, Bihua, He, Juan, Shan, Hongying, Zhou, Gengmin, Wang, Deli, Bai, Lu, Shang, Hongxi, Nie, Liping, Pan, Fan, Lan, Hui Yao, Wang, Qingwen
• Format: Article
• Language: English
• Subjects: Animals; Arthritis, Rheumatoid - drug therapy; CD4-Positive T-Lymphocytes - immunology; DNA - therapeutic use; DNA Methylation; DNA methyltransferase; hypermethylation; Immunology; Interleukin-6 - genetics; methyl-CpG binding domain; Mice; rheumatoid arthritis; Smad7; T-Lymphocytes, Regulatory
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2023.1104881

Smad7 is protective in a mouse model of rheumatoid arthritis. Here we investigated whether Smad7-expressing CD4 T cells and the methylation of gene in CD4 T cells contribute to the disease activity of RA in patients. Peripheral CD4 T cells were collected from 35 healthy controls and 57 RA patients. Smad7 expression by CD4 T cells were determined and correlated with the clinical parameters of RA including RA score and serum levels of IL-6, CRP, ESR, DAS28-CRP, DAS28-ESR, Swollen joints and Tender joints. Bisulfite sequencing (BSP-seq) was used to determine the DNA methylation in Smad7 promoter (-1000 to +2000) region in CD4 T cells. In addition, a DNA methylation inhibitor, 5-Azacytidine (5-AzaC), was added to CD4 T cells to examine the possible role of Smad7 methylation in CD4 T cell differentiation and functional activity. Compared to the heath controls, Smad7 expression was significantly decreased in CD4 T cells from RA patients and inversely correlated with the RA activity score and serum levels of IL-6 and CRP. Importantly, loss of Smad7 in CD4 T cell was associated with the alteration of Th17/Treg balance by increasing Th17 over the Treg population. BSP-seq detected that DNA hypermethylation occurred in the Smad7 promoter region of CD4 T cells obtained from RA patients. Mechanistically, we found that the DNA hypermethylation in the Smad7 promoter of CD4 T cells was associated with decreased Smad7 expression in RA patients. This was associated with overreactive DNA methyltransferase (DMNT1) and downregulation of the methyl-CpG binding domain proteins (MBD4). Inhibition of DNA methylation by treating CD4 T cells from RA patients with 5-AzaC significantly increased Smad7 mRNA expression along with the increased MBD4 but reduced DNMT1 expression, which was associated with the rebalance in the Th17/Treg response. DNA hypermethylation at the Smad7 promoter regions may cause a loss of Smad7 in CD4 T cells of RA patients, which may contribute to the RA activity by disrupting the Th17/Treg balance.