Giordano Andrea, Cencioni Luciano, Salvo Domenica Paola, Berrettini Mauro
U.O. Nefrologia e Dialisi, P.O. Orvieto, Orvieto.
G Ital Nefrol. 2011 Mar-Apr;28(2):214-8.
We report the case of a patient with rheumatoid arthritis (RA) who developed a membranous nephropathy (MN) with nephrotic syndrome while receiving etanercept, a fusion protein that binds specifically to TNFalpha and blocks its interaction with TNFalpha receptors. A 62-year-old man with RA treated with etanercept was admitted to our unit in March 2008 because of a full-blown nephrotic syndrome. Renal biopsy showed a typical MN. Since no improvement of proteinuria was observed after withdrawal of etanercept, we administered rituximab (1 g two weeks apart repeated after 6 months). The signs and symptoms of RA improved and proteinuria decreased from 7.2 g/24h to 2.3 g/24h. MN is an immunological glomerulonephritis that may complicate other immune-mediated diseases or may be triggered by a number of drugs. The clinical improvement of both RA and MN after rituximab may indirectly confirm the role of antibodies in the pathogenesis of these diseases, although the mechanisms of action of this drug in immunological disorders remain to be elucidated.
我们报告了一例类风湿关节炎(RA)患者的病例,该患者在接受依那西普治疗时出现了伴有肾病综合征的膜性肾病(MN)。依那西普是一种融合蛋白,可特异性结合肿瘤坏死因子α(TNFα)并阻断其与TNFα受体的相互作用。一名接受依那西普治疗的62岁RA男性患者于2008年3月因出现典型的肾病综合征入住我院。肾活检显示为典型的MN。停用依那西普后蛋白尿未见改善,我们给予利妥昔单抗(1 g,间隔两周,6个月后重复给药)。RA的症状和体征有所改善,蛋白尿从7.2 g/24小时降至2.3 g/24小时。MN是一种免疫性肾小球肾炎,可能并发于其他免疫介导的疾病,或由多种药物引发。利妥昔单抗治疗后RA和MN的临床改善可能间接证实了抗体在这些疾病发病机制中的作用,尽管该药物在免疫性疾病中的作用机制仍有待阐明。