CD8 + Regulatory T Cell Deficiency in Elderly-Onset Rheumatoid Arthritis.
Ryu WatanabeKeiichiro KadobaAtsuko TamamotoKoichi MurataKosaku MurakamiHideo OnizawaTakayuki FujiiAkira OnishiMasao TanakaHiromu ItoAkio MorinobuMotomu HashimotoPublished in: Journal of clinical medicine (2023)
Elderly-onset rheumatoid arthritis (EORA) is associated with higher disease activity and accelerated joint destruction compared with young-onset RA (YORA). However, the underlying immunological mechanism remains unclear. Regulatory T cells (Tregs) are an immunosuppressive T cell subset, and CD4 + Tregs are deficient and/or dysfunctional in RA; however, CD8 + Tregs have not been fully examined in RA. Here, we aimed to determine the role of CD8 + Tregs, particularly in EORA. A total of 40 patients (EORA, n = 17; YORA, n = 23) were cross-sectionally enrolled. Current disease activity and treatment were comparable between the two groups; however, levels of multiple cytokines, including IL-1β, TNFα, interferon (IFN)-γ, IL-2, and IL-10, were significantly increased in EORA. The number of CD4 + Tregs did not differ between the groups ( p = 0.37), but those of CD8 + Tregs were significantly decreased in EORA ( p = 0.0033). The number of CD8 + Tregs were inversely correlated with plasma matrix metalloprotease (MMP)-3 levels (r = -0.3331, p = 0.036). Our study results revealed an intrinsic deficiency of CD8 + Tregs in patients with EORA, which leaves synovitis unchecked with excessive MMP-3 release. A therapeutic approach to restore CD8 + Tregs may provide a new avenue for the treatment of EORA.
Keyphrases
- rheumatoid arthritis
- disease activity
- systemic lupus erythematosus
- ankylosing spondylitis
- regulatory t cells
- rheumatoid arthritis patients
- nk cells
- juvenile idiopathic arthritis
- immune response
- dendritic cells
- ejection fraction
- body mass index
- idiopathic pulmonary fibrosis
- middle aged
- transcription factor
- peritoneal dialysis