Low-Dose Radiotherapy Attenuates Experimental Autoimmune Arthritis by Inducing Apoptosis of Lymphocytes and Fibroblast-Like Synoviocytes.
Bo-Gyu KimHoon Sik ChoiYong-Ho ChoeHyun Min JeonJi Yeon HeoYun-Hong CheonKi Mun KangSang Il LeeBae Kwon JeongMingyo KimPublished in: Immune network (2024)
Low-dose radiotherapy (LDRT) has been explored as a treatment option for various inflammatory diseases; however, its application in the context of rheumatoid arthritis (RA) is lacking. This study aimed to elucidate the mechanism underlying LDRT-based treatment for RA and standardize it. LDRT reduced the total numbers of immune cells, but increased the apoptotic CD4 + T and B220 + B cells, in the draining lymph nodes of collagen induced arthritis and K/BxN models. In addition, it significantly reduced the severity of various pathological manifestations, including bone destruction, cartilage erosion, and swelling of hind limb ankle. Post-LDRT, the proportion of apoptotic CD4 + T and CD19 + B cells increased significantly in the PBMCs derived from human patients with RA. LDRT showed a similar effect in fibroblast-like synoviocytes as well. In conclusion, we report that LDRT induces apoptosis in immune cells and fibro-blast-like synoviocytes, contributing to attenuation of arthritis.
Keyphrases
- rheumatoid arthritis
- low dose
- disease activity
- cell death
- lymph node
- early stage
- interstitial lung disease
- ankylosing spondylitis
- endothelial cells
- oxidative stress
- high dose
- radiation therapy
- nk cells
- high glucose
- bone mineral density
- systemic lupus erythematosus
- postmenopausal women
- cell cycle arrest
- pluripotent stem cells
- induced pluripotent stem cells
- pi k akt
- stress induced