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During the congress, E-Posters will be accessible to all participants on the congress website 24/7, as well as in the E-poster stations in the congress center.
Preparing your E-Poster
Please review the E-Poster format requirements carefully when preparing your E-Poster. Should your E-Poster not meet the mentioned requirements, it may not be displayed as described above.
E-Poster Submission Deadline
Please prepare and upload your E-Poster no later than March 14, 2026 11.59PM CET. After this date, you will no longer be able to prepare and upload your E-poster and it will not be displayed and accessible on the congress website.
Please follow the instructions below to input your abstract title.
Abstract titles should be brief and reflect the content of the abstract.
Immunoglobulin A nephropathy (IgAN) is the most common primary glomerular disease worldwide, and there remains a need for effective and safe treatment options. Telitacicept is a novel fusion protein that simultaneously inhibits BLyS and APRIL. Preliminary studies have demonstrated its significant efficacy in autoimmune diseases. However, its effectiveness and safety in the treatment of IgAN, as well as the serum biomarkers that can be used to evaluate treatment response, require further validation through real-world studies.
This retrospective, single-arm cohort study included patients with high-risk progressive IgAN who received telitacicept combined with low-dose steroids. Clinical and laboratory data were collected from treatment initiation to 12 months to assess the treatment response. Levels of BAFF, APRIL, and Gd-IgA1 were measured to analyze the relationship between the changes in these markers and proteinuria reduction.
A total of 40 patients were included. At 6 months of Telitacicept treatment, urinary protein decreased by 48.23% (Z = -4.869, P < 0.001); at 12 months, it decreased by 83.11% (Z = -2.666, P = 0.008). Renal function remained stable during the follow-up period, and no serious adverse reactions were observed. Compared with healthy controls, IgAN patients had significantly higher serum levels of BAFF, APRIL, and Gd-IgA1. After 6 months of treatment, BAFF decreased by 37.19% (t = 6.141, P < 0.001), APRIL decreased by 38.56% (t = 9.927, P < 0.001), and Gd-IgA1 decreased by 63.00% (Z = 3.516, P < 0.001). Compared to BAFF (AUC = 0.590, P = 0.278) and APRIL (AUC = 0.678, P = 0.031), serum Gd-IgA1 (AUC = 0.716, P = 0.009) was more effective in evaluating clinical remission.
Telitacicept significantly reduces urinary protein levels in IgAN patients with a favorable safety profile during treatment. Compared to BAFF and APRIL, Gd-IgA1 shows greater value in assessing treatment response in IgAN patients.