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Background: Abnormal autoimmunity occur before the onset of clinical rheumatoid arthritis(RA)1. Soluble interleukin-2 receptor (sIL-2R) is an indicator of immune activation in the body, which may be related to the activity, prognosis, and response to treatment of the disease2, 3. Early identification in the undifferentiated arthritis(UA) is crucial for precision therapy. In order to explore the predictive value of sIL-2R for the development of patients with UA. Objectives: We included seropositive patients (ACPA positive with or without RF positive) with undifferentiated arthritis (UA, n=27), early RA patients (Ea-RA, n=40), newly diagnosed RA patients (new RA, n=60), and patients who had been treated were readmitted due to disease activity (Relapsed RA, Re-RA, n=50). 45 healthy controls(HC) matched by sex and age were also included. Serum levels of IL-2, IL-4, IL-6, IL-10, IL-17, IFN-γ, and TNF-α were detected by magnetic bead multiplex immunofluorescence assay using human Th1/Th2/Th17 subsets detection kit. The level of sIL-2R was analyzed by ELISA. Methods: We included seropositive patients with undifferentiated arthritis (UA, n=27), early RA patients (Ea-RA, n=40), newly diagnosed RA patients (new RA, n=60), and patients who had been treated were readmitted due to disease activity (Relapsed RA, Re-RA, n=50). 45 healthy controls(HC) matched by sex and age were also included. Serum levels of IL-2, IL-4, IL-6, IL-10, IL-17, IFN-γ, and TNF-α were detected by magnetic bead multiplex immunofluorescence assay using human Th1/Th2/Th17 subsets detection kit. The level of sIL-2R was analyzed by ELISA. Results: The results showed that the serum levels of IL-2, IL-4 and IL-17 in UA, Ea-RA, New RA and Re-RA groups were significantly higher than those in HC, and the levels of IL-4 in Ea-RA and New-RA groups were increased than those in Re-RA. Moreover, the levels of IL-10, IFN-γ and TNF-α in Ea-RA, New-RA and Re-RA groups were elevated, while UA group showed no statistical difference, while the levels of IL-6 in New-RA and Re-RA groups were significantly higher than those in healthy controls. Additionally, the level of sIL-2R in the UA group was not significantly higher than that in the healthy control group, while the Ea-RA, New-RA and Re-RA groups were significantly higher than that in the HC and the UA group. In order to further assess predictive value in UA and early RA, we conducted ROC curve analysis, with an area under the curve (AUC) of 0.7952, (95% CI 0.6820 to 0.9084, pConclusion: Elevated levels of sIL-2R in the undifferentiated stage of arthritis may indicate the possibility of progression, which has reference value for guiding treatment. REFERENCES: 1 van Steenbergen HW, Cope AP, van der Helm-van Mil AHM.Rheumatoid arthritis prevention in arthralgia: fantasy or reality? Nat Rev Rheumatol.2023;19(12): 767-777. 2 Damoiseaux J.The IL-2 - IL-2 receptor pathway in health and disease: The role of the soluble IL-2 receptor. Clin Immunol.2020;218:108515. 3 van Steenbergen HW, van Nies JA, Ruyssen-Witrand A, Huizinga TW, Cantagrel A, Berenbaum F, et al.IL2RA is associated with persistence of rheumatoid arthritis. Arthritis Res Ther.2015;17(1): 244. Acknowledgements: NIL. Disclosure of Interests: None declared.
Wang et al. (Sat,) studied this question.
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