Efficacy and safety of telitacicept as an add-on therapy for relapsing lupus nephritis: a retrospective cohort study

医学 狼疮性肾炎 内科学 回顾性队列研究 入射(几何) 糖皮质激素 系统性红斑狼疮 不利影响 累积发病率 比例危险模型 队列研究 多元分析 疾病 红斑狼疮 队列 强的松 泌尿系统 临床试验 随机对照试验 结缔组织病 胃肠病学 免疫学 联合疗法 蛋白尿 外科
作者
Cui Wang,Xue Bai,Jiawen Li,Jie Zhao,Yarui Zhang,Xuehong Lu,Qiaoyan Guo
出处
期刊:Frontiers in Immunology [Frontiers Media]
卷期号:17: 1826829-1826829
标识
DOI:10.3389/fimmu.2026.1826829
摘要

Aim: This study aims to evaluate the efficacy and safety of telitacicept addition to standard therapy in adults with relapsing lupus nephritis (LN). Methods: From 2021 to 2024, patients with relapsing LN were identified and divided into two groups based on telitacicept administration. Laboratory indicators, renal remission status, Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) scores, glucocorticoid dosages, and the incidence of renal flares were evaluated. Multivariate regression was used to assess the baseline predictors of complete renal remission (CRR) and adverse events (AEs) were recorded. Results: Compared to the standard therapy group (n=20), the proportion of patients who achieved a CRR and the primary efficacy renal response were significantly increased in the telitacicept group (n=20) at 6, 9, and 12 months, while the reduction rates of 24-hour urinary protein from baseline at 1, 3, and 9 months were significantly higher. The telitacicept group showed notable improvement in treatment responses in the median SLEDAI-2K score and glucocorticoid dose. Multivariate Cox regression analysis revealed that add-on telitacicept was associated with achieving early CRR. At the end of the follow-up period, the cumulative relapse rate in the telitacicept group was significantly lower than that in the standard treatment group, with no increase in the incidence of AEs. Conclusions: As an add-on therapy, telitacicept is associated with early disease remission in patients with relapsing LN with reduced disease activity, lower glucocorticoid dosage, and fewer relapses. It also showed a favorable safety profile.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
孤独手机发布了新的文献求助10
刚刚
1秒前
隐形曼青的应助被lxl采纳,获得10
1秒前
heaven发布了新的文献求助10
1秒前
怕黑笑旋发布了新的文献求助10
2秒前
tcf的应助被lucky采纳,获得10
2秒前
默默曼安发布了新的文献求助10
2秒前
2秒前
哈哈哈发布了新的文献求助10
3秒前
可乐发布了新的文献求助10
3秒前
科研通AI6.2的应助被艾利威尔采纳,获得10
3秒前
Jasper的应助被无辜的发带采纳,获得10
4秒前
abcowc发布了新的文献求助10
4秒前
biu发布了新的文献求助10
5秒前
5秒前
小懒虫发布了新的文献求助10
8秒前
jin的应助被左白易采纳,获得10
8秒前
陈哥发布了新的文献求助10
8秒前
唐唐发布了新的文献求助10
9秒前
迷路的依波完成签到,获得积分10
9秒前
Chauncy完成签到,获得积分10
9秒前
10秒前
10秒前
所所的应助被新材料采纳,获得10
10秒前
Momo01的应助被zero采纳,获得10
11秒前
火星上清炎的应助被走四方采纳,获得10
11秒前
12秒前
hjygzv完成签到,获得积分10
12秒前
以舟完成签到,获得积分10
12秒前
12秒前
小马甲的应助被Chauncy采纳,获得10
13秒前
在水一方的应助被嘻嘻采纳,获得10
13秒前
乐乐的应助被嘻嘻采纳,获得10
13秒前
14秒前
简单的灵槐完成签到,获得积分20
15秒前
15秒前
追忆发布了新的文献求助10
15秒前
陈陈陈完成签到,获得积分10
16秒前
16秒前
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
CODESSA 2000
Rosenblum, Global Change Biology 800
Berberine regulates the TLR4 signaling pathway to suppress hypoxia-induced proliferation and migration of pulmonary arterial smooth muscle cells 520
Organizational Behavior 510
The Welfare Assembly Line: Public Servants in the Suffering City 500
Polymer-based Membranes for Separation and Recovery of Precious Metals 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 有机化学 化学工程 内科学 物理 生物化学 复合材料 催化作用 细胞生物学 人工智能 心理学 无机化学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 7849159
求助须知:如何正确求助?哪些是违规求助? 9368981
关于积分的说明 20665522
捐赠科研通 7446337
什么是DOI,文献DOI怎么找? 3342655
关于科研通互助平台的介绍 2486227
邀请新用户注册赠送积分活动 2365855