Geetha Duvuru, Kallenberg Cees, Stone John H, Salama Alan D, Appel Gerald B, Duna George, Brunetta Paul, Jayne David
Division of Nephrology, Johns Hopkins University School of Medicine, Johns Hopkins Bayview Medical Center, 301 Mason Lord Drive, Suite 2500, Baltimore, MD, USA,
J Nephrol. 2015 Feb;28(1):17-27. doi: 10.1007/s40620-014-0135-3. Epub 2014 Sep 4.
Granulomatosis with polyangiitis and microscopic polyangiitis are anti-neutrophil cytoplasmic antibody-associated vasculitides (AAVs) that are prone to cycles of remission and relapse. The introduction of cytotoxic therapy has changed the prognosis for these diseases from typically fatal to manageable chronic illnesses with a relapsing course. Despite improvements in outcomes, recurrence of disease and drug-related toxicity continue to produce significant morbidity and mortality. Better understanding of the pathogenesis of AAV and the mechanism of action of cyclophosphamide has led to investigation of therapies that target B cells. Two randomized controlled trials have shown that rituximab is not inferior to cyclophosphamide for induction of remission in severe AAV, with no significant difference in the incidence of overall adverse events in rituximab- versus cyclophosphamide-treated patients. Data from ongoing clinical trials will determine the role of rituximab in the maintenance of remission.
肉芽肿性多血管炎和显微镜下多血管炎是抗中性粒细胞胞浆抗体相关性血管炎(AAV),易于缓解和复发。细胞毒性疗法的引入已将这些疾病的预后从通常致命转变为可控制的慢性复发性疾病。尽管治疗效果有所改善,但疾病复发和药物相关毒性仍会导致显著的发病率和死亡率。对AAV发病机制和环磷酰胺作用机制的深入了解促使人们对靶向B细胞的疗法进行研究。两项随机对照试验表明,在诱导重症AAV缓解方面,利妥昔单抗并不劣于环磷酰胺,利妥昔单抗治疗组与环磷酰胺治疗组的总体不良事件发生率无显著差异。正在进行的临床试验数据将确定利妥昔单抗在维持缓解中的作用。