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补体C5抑制剂依库珠单抗在系统性硬化病合并肾危象中的应用进展

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摘要 系统性硬化病(SSc)合并肾危象是SSc的一种罕见的严重并发症,临床上主要表现为突然出现血压升高、急性肾衰竭和血栓性微血管病变,是导致SSc患者死亡的主要原因之一。早期诊断后积极应用血管紧张素转换酶抑制剂(ACEI)控制血压可改善预后,但仍有大多数患者治疗效果不理想,肾功能持续恶化,总体结局较差。这种疾病的病因及发病机制尚不明确,但有越来越多的证据表明补体系统的异常激活可能参与其中,早期应用补体C5抑制剂依库珠单抗可有效阻断补体系统活化,对难治性SSc肾危象患者可能具有治疗潜力。
出处 《中华风湿病学杂志》 CAS CSCD 北大核心 2023年第11期785-788,共4页 Chinese Journal of Rheumatology
基金 河南省医学科技攻关计划联合共建项目(LHGJ20210280)。
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  • 1Botto M, Kirschfink M, Macor P, et al. Complement in hu- man diseases., lessons from complement deficiencies [J]. Mol Immunol, 2009, 46(14): 2774-2783.
  • 2Schmidtko J, Peine S, EL-Housseini Y, et al. Treatment of atypical hemolytic uremic syndrome and thrombotic microan- giopathies., a focus on eculizumab [J]. Am J Kidney Dis, 2013, 61(2):289-299.
  • 3McRae JL, Duthy TG, Griggs KM, et al. Human factor H- related protein 5 has cofactor activity, inhibits C3 convertase activity, binds heparin and C-reactive protein, and associates with lipoprotein [J]. J Immunol, 2005, 174(10):6250-6256.
  • 4Constantinescu AR, Bitzan M, Weiss LS, et al. Non- enteropathic hemolytic uremic syndrome:causes and short- term course [J]. Am J Kidney Dis, 2004,43(6): 976-982.
  • 5Campistol JM, Arias M, Ariceta G, et al. An update for atypical haemolytic uraemic syndrome: diagnosis and treat- ment. A consensus document [J]. Nefrologia, 2013,33 (1): 27-45.
  • 6Noris M, Caprioli J, Bresin E, et al. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype [J]. Clin J Am Soc Nephrol, 2010,5(10): 1844-1859.
  • 7Westra D, Volokhina E, van der Heijden E, et al. Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS) [J]. Nephrol Dial Transplant, 2010, 25(7): 2195-2202.
  • 8Bienaime F, Dragon-Durey MA, Regnier CH, et al. Muta- tions in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome [J]. Kidney Int, 2010, 77(4): 339-349.
  • 9Dragon-Durey MA, Sethi SK, Bagga A, et aL Clinical fea- tures of anti-factor H autoantibody-associated hemolytic ure- mic syndrome [J]. JAm Soc Nephrol,2010,21(12):2180-2187.
  • 10Orth D, W0rzner R. Complement in typical hemolytic uremic syndrome [J]. Semin Thromb Hemost, 2010, 36(6): 620-624.

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