Trivioli Giorgio, Casal Moura Marta, Kronbichler Andreas, Smith Rona M, Terrier Benjamin, McAdoo Stephen, Jones Rachel B, Merkel Peter A, Jayne David R W
Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Department of Medicine, University of Cambridge, Cambridge, UK.
Nat Rev Rheumatol. 2025 Jun 5. doi: 10.1038/s41584-025-01266-1.
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) consists of a group of small-vessel vasculitides that often present with organ-threatening or life-threatening manifestations. Current immunosuppressive treatments have improved survival and rates of remission, but are not curative, have frequent toxicities, and do not effectively prevent relapse. Clinical trials have established the role of rituximab, an anti-CD20 B cell-depleting monoclonal antibody, in both the remission-induction and maintenance phases of the disease and demonstrated that glucocorticoid doses can be substantially reduced from historical dosing levels without affecting treatment efficacy. Therapies that have the potential to be more effective and safer have become available or are under investigation. Avacopan, an oral C5a receptor antagonist, was approved as an adjunctive treatment for AAV and use of this drug in combination with rituximab or cyclophosphamide and markedly reduced glucocorticoid dosing demonstrated superior efficacy and potentially greater kidney recovery than prior standard of care. Other agents under study for treatment of AAV include next-generation anti-CD20 monoclonal antibodies, anti-CD19 chimeric antigen receptor T cells, novel complement inhibitors and agents that can target fibrosis. Alongside traditional randomized controlled trials with clinical endpoints, experimental medicine studies are focusing on mechanistic endpoints and disease biomarkers. This Review discusses current treatments and the advances in the management of AAV.
抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)是一组小血管炎,常表现为威胁器官或生命的症状。目前的免疫抑制治疗提高了生存率和缓解率,但并非治愈性治疗,常有毒性,且不能有效预防复发。临床试验已证实利妥昔单抗(一种抗CD20 B细胞耗竭性单克隆抗体)在该疾病的诱导缓解期和维持期均有作用,并表明糖皮质激素剂量可从既往给药水平大幅降低而不影响治疗效果。更有效、更安全的治疗方法已可获得或正在研究中。阿伐可泮是一种口服C5a受体拮抗剂,已被批准作为AAV的辅助治疗药物,该药物与利妥昔单抗或环磷酰胺联合使用,并显著降低糖皮质激素剂量,显示出比既往标准治疗更高的疗效和可能更好的肾脏恢复效果。其他正在研究用于治疗AAV的药物包括新一代抗CD20单克隆抗体、抗CD19嵌合抗原受体T细胞、新型补体抑制剂以及可靶向纤维化的药物。除了以临床终点为指标的传统随机对照试验外,实验医学研究正聚焦于机制性终点和疾病生物标志物。本综述讨论了AAV的当前治疗方法及管理进展。