Melander Catherine, Sallée Marion, Trolliet Pierre, Candon Sophie, Belenfant Xavier, Daugas Eric, Rémy Phillipe, Zarrouk Virginie, Pillebout Evangéline, Jacquot Christian, Boffa Jean-Jacques, Karras Alexandre, Masse Virginie, Lesavre Philippe, Elie Caroline, Brocheriou Isabelle, Knebelmann Bertrand, Noël Laure-Hélène, Fakhouri Fadi
Department of Nephrology, Assistance Publique-Hôpitaux Paris, Université Paris Descartes, Hôpital Necker, Paris, France.
Clin J Am Soc Nephrol. 2009 Mar;4(3):579-87. doi: 10.2215/CJN.04030808. Epub 2009 Mar 4.
Standard treatment for lupus nephritis, including corticosteroids and cyclophosphamide, is efficient but is still associated with refractory or relapsing disease, or severe deleterious effects. Rituximab, a monoclonal chimeric anti-B cell antibody, is increasingly used in patients with lupus nephritis, but reported series were small and had a short follow-up.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: The authors analyzed clinical and histologic data of 20 patients who were treated with rituximab for lupus nephritis and followed up for at least 12 mo.
Nineteen women and one man received rituximab as induction treatment for an active class IV (15 cases) or class V (5 cases) lupus nephritis. Rituximab was given for lupus nephritis refractory to standard treatment (12 cases), for relapsing disease (6 cases), or as first-line treatment (2 cases). Three patients received cyclophosphamide concomitantly with rituximab. Ten received new injections of rituximab as maintenance therapy. Side effects included mainly five infections and four moderate neutropenias. After a median follow-up of 22 mo, complete or partial renal remission was obtained in 12 patients (60%). Lupus nephritis relapsed in one patient, who responded to a new course of rituximab. The achievement of B cell depletion 1 mo after rituximab, which negatively correlated with black ethnicity and hypoalbuminemia, was strongly associated with renal response. Rapidly progressive glomerulonephritis did not respond to rituximab.
Rituximab is an interesting therapeutic option in relapsing or refractory lupus nephritis when early B cell depletion is obtained.
狼疮性肾炎的标准治疗方法,包括使用皮质类固醇和环磷酰胺,虽有疗效,但仍与难治性或复发性疾病,或严重有害效应相关。利妥昔单抗是一种嵌合单克隆抗B细胞抗体,越来越多地用于狼疮性肾炎患者,但已报道的病例系列规模较小且随访时间较短。
设计、地点、参与者及测量指标:作者分析了20例接受利妥昔单抗治疗狼疮性肾炎且随访至少12个月的患者的临床和组织学数据。
19名女性和1名男性接受利妥昔单抗作为活动性IV级(15例)或V级(5例)狼疮性肾炎的诱导治疗。利妥昔单抗用于标准治疗难治的狼疮性肾炎(12例)、复发性疾病(6例)或作为一线治疗(2例)。3例患者在使用利妥昔单抗的同时接受了环磷酰胺治疗。10例患者接受了新的利妥昔单抗注射作为维持治疗。副作用主要包括5次感染和4次中度中性粒细胞减少。中位随访22个月后,12例患者(60%)获得了完全或部分肾脏缓解。1例患者狼疮性肾炎复发,对新一轮利妥昔单抗治疗有反应。利妥昔单抗治疗1个月后B细胞耗竭的实现与黑人种族和低白蛋白血症呈负相关,与肾脏反应密切相关。快速进展性肾小球肾炎对利妥昔单抗无反应。
当早期实现B细胞耗竭时,利妥昔单抗是复发性或难治性狼疮性肾炎的一种有吸引力的治疗选择。