蛋白尿
医学
不利影响
内科学
胃肠病学
生物标志物
泌尿系统
肾病
尿
子群分析
淋巴细胞
免疫学
抗体
糖皮质激素
自身免疫性疾病
免疫病理学
蛋白尿
泌尿科
疾病
免疫球蛋白G
毒性
显著性差异
微小变化病
免疫系统
临床意义
肾小球肾炎
肾脏疾病
作者
Yan Yang,Yafei Chen,Xialian Xu,Shi Jin,Ziyan Shen,Yao Meng,Shaomin Gong,Jie Yu,Han Zhang,Yong Li,Shengzhuo You,X Zou,Yi Fang,Xiaoqiang Ding,Yiqin Shi
标识
DOI:10.1096/fj.202504771r
摘要
Telitacicept, a novel fusion protein that targets B lymphocyte stimulator and a proliferation-inducing ligand, has been used in autoimmune diseases. However, the efficacy and safety of telitacicept combined with glucocorticoids (GCs) in the treatment of immunoglobulin A nephropathy (IgAN) remain unclear. We recruited a total of 71 IgAN patients who received telitacicept without concurrent immunosuppressive therapy. Among them, 40 patients who received telitacicept 160 mg weekly and had not received GCs within the previous 3 months were further analyzed. Patients treated with telitacicept alone formed the telitacicept-alone subgroup, while those who received telitacicept plus GCs formed the telitacicept + GC subgroup. The primary outcome was the change in 24-h proteinuria from baseline over time. The telitacicept + GC subgroup showed a greater reduction in mean proteinuria (-84.1%, IQR: -90.4% to -74.4%) compared with the telitacicept-alone subgroup (-71.4%, IQR: -88.5% to -33.5%; p = 0.043) at 6 months. The eGFR slightly increased with no significant difference (8.8% vs. 8.1%; p = 0.91). Both groups showed reductions in serum IgA, IgG levels, and the percentage of patients with hematuria. Urinary soluble CD163, a potential biomarker of disease activity, also significantly decreased following telitacicept treatment (-4.33 ng/mg; p = 0.001). No serious adverse events were reported. In conclusion, telitacicept combined with glucocorticoids may offer a greater reduction in proteinuria than telitacicept monotherapy in IgAN patients, with preserved renal function. These findings support potential benefit of adjunctive GC therapy in selected patients undergoing telitacicept treatment.
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