Massachusettes General Hospital, Boston, USA.
Clin Exp Immunol. 2011 May;164 Suppl 1(Suppl 1):27-30. doi: 10.1111/j.1365-2249.2011.04363.x.
Anti-neutrophil cytoplasmic antibodies (ANCA) have been associated with a spectrum of vasculitis that includes granulomatous polyangiitis (formerly known as Wegener's granulomatosis), microscopic polyangiitis, the Churg-Strauss syndrome, primary pauciimmune necrotizing and crescentic glomerulonephritis and related forms of vasculitis. In vitro, in vivo and clinical evidence support the conclusion that ANCA participate in the pathophysiology of this disease spectrum. Rituximab is a potent tool that can interrupt B cell-mediated immunity without major compromise of T cell-mediated immunity. Thus, it has great appeal as a tool to interrupt antibody-mediated autoimmune disease. The results of two prospective randomized trials confirm that rituximab can be effective as part of induction therapy for active ANCA-associated vasculitis. The safety profile for rituximab appears favourable relative to cyclophosphamide and steroids. However, there remain many patients who require individualized adjustments of ancillary therapy, as breakthrough disease, relapses and infectious complications do occur. Based on our current knowledge, rituximab should now be incorporated as part of induction therapy in many patients with ANCA-associated vasculitis. However, more work is needed to determine how rituximab may best be integrated into the overall immunosuppression of these patients.
抗中性粒细胞胞质抗体(ANCA)与多种血管炎相关,包括肉芽肿性多血管炎(以前称为韦格纳肉芽肿病)、显微镜下多血管炎、Churg-Strauss 综合征、原发性少免疫性坏死性和新月体性肾小球肾炎及相关形式的血管炎。体外、体内和临床证据支持这样的结论,即 ANCA 参与了这一疾病谱的病理生理过程。利妥昔单抗是一种有效的工具,可以在不严重影响 T 细胞介导免疫的情况下阻断 B 细胞介导的免疫。因此,它作为一种阻断抗体介导的自身免疫性疾病的工具具有很大的吸引力。两项前瞻性随机试验的结果证实,利妥昔单抗可以作为活性 ANCA 相关性血管炎诱导治疗的一部分有效。与环磷酰胺和类固醇相比,利妥昔单抗的安全性特征似乎更好。然而,仍有许多患者需要对辅助治疗进行个体化调整,因为突破性疾病、复发和感染并发症确实会发生。基于我们目前的知识,利妥昔单抗现在应该作为许多 ANCA 相关性血管炎患者诱导治疗的一部分。然而,还需要更多的工作来确定利妥昔单抗如何才能最好地整合到这些患者的整体免疫抑制治疗中。