Saegusa Kazusa, Tsuchida Yumi, Komai Toshihiko, Tsuchiya Haruka, Fujio Keishi
Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
Int J Mol Sci. 2025 Jan 23;26(3):929. doi: 10.3390/ijms26030929.
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with diverse clinical manifestations that can lead to severe organ damage. The complex pathophysiology of SLE makes treatment selection difficult. This review examines the current evidence for biological therapies in SLE, including the anti-B cell activating factor antibody belimumab; the type I interferon receptor antagonist anifrolumab; the novel calcineurin inhibitor voclosporin; and rituximab, which targets CD20 on B cells. We also describe emerging therapies, including novel agents in development and CD19-directed chimeric antigen receptor (CAR) T cell therapy, which has shown promise in early clinical experience. Recent advances in biomarker research, including interferon signatures and transcriptomic profiles, may facilitate patient stratification and treatment selection. This review offers insights into current and future treatment strategies for patients with SLE by analyzing clinical trial results and recent immunological findings.
系统性红斑狼疮(SLE)是一种临床表现多样的慢性自身免疫性疾病,可导致严重的器官损害。SLE复杂的病理生理学使得治疗方案的选择颇具难度。本综述探讨了SLE生物疗法的现有证据,包括抗B细胞活化因子抗体贝利尤单抗;I型干扰素受体拮抗剂阿尼鲁单抗;新型钙调神经磷酸酶抑制剂voclosporin;以及靶向B细胞上CD20的利妥昔单抗。我们还描述了新兴疗法,包括正在研发的新型药物以及CD19导向的嵌合抗原受体(CAR)T细胞疗法,后者在早期临床经验中已显示出前景。生物标志物研究的最新进展,包括干扰素特征和转录组谱,可能有助于患者分层和治疗选择。本综述通过分析临床试验结果和近期免疫学发现,为SLE患者当前和未来的治疗策略提供见解。