Literature DB >> 23486421

Eculizumab in the treatment of atypical haemolytic uraemic syndrome and other complement-mediated renal diseases.

Carla M Nester1, Patrick D Brophy.   

Abstract

PURPOSE OF REVIEW: This review considers the use of eculizumab in the treatment of atypical haemolytic uraemic syndrome (aHUS) as well as the other complement-mediated renal diseases, including dense deposit disease (DDD) and C3 glomerulonephritis (C3GN). In addition, a brief discussion of the effectiveness of eculizumab for the prevention of antibody-mediated rejection (AMR) in the setting of renal transplant and the treatment of shiga toxin associated haemolytic uraemic syndrome (STEC HUS) is also provided. RECENT
FINDINGS: No randomized controlled trials exist to support the use of eculizumab in renal disease. The results of two unpublished, prospective adult and adolescent trials support its utility in aHUS, whereas retrospective data support the effectiveness in paediatric aHUS. These two data sets form the basis of the sole renal indication for eculizumab. One small, single-centre trial and a growing number of case reports support the use of eculizumab in C3 glomerulopathy (C3G). There are limited trial data in AMR and renal transplant. Finally, there are conflicting data for the use of eculizumab in STEC HUS.
SUMMARY: The cumulative published data establish the effectiveness of eculizumab in a select group of renal diseases that have at the centre of their disease either abnormal complement control or maladaptive complement activation.

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Year:  2013        PMID: 23486421     DOI: 10.1097/MOP.0b013e32835df4a3

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  12 in total

Review 1.  The Evolving Landscape for Complement Therapeutics in Rheumatic and Autoimmune Diseases.

Authors:  Joshua M Thurman; Ashley Frazer-Abel; V Michael Holers
Journal:  Arthritis Rheumatol       Date:  2017-10-17       Impact factor: 10.995

2.  Two cases of atypical hemolytic uremic syndrome (aHUS) and eosinophilic granulomatosis with polyangiitis (EGPA): a possible relationship.

Authors:  Mercedes Cao; Tamara Ferreiro; Bruna N Leite; Francisco Pita; Luis Bolaños; Francisco Valdés; Angel Alonso; Eduardo Vázquez; Juan Mosquera; María Trigás; Santiago Rodríguez
Journal:  CEN Case Rep       Date:  2017-03-01

3.  Local Inhibition of Complement Improves Mesenchymal Stem Cell Viability and Function After Administration.

Authors:  Yan Li; John Fung; Feng Lin
Journal:  Mol Ther       Date:  2016-07-05       Impact factor: 11.454

Review 4.  New milestones ahead in complement-targeted therapy.

Authors:  Daniel Ricklin; John D Lambris
Journal:  Semin Immunol       Date:  2016-06-16       Impact factor: 11.130

Review 5.  Complement cascade and kidney transplantation: The rediscovery of an ancient enemy.

Authors:  Alberto Mella; Maria Messina; Antonio Lavacca; Luigi Biancone
Journal:  World J Transplant       Date:  2014-09-24

6.  Monitoring of complement activation biomarkers and eculizumab in complement-mediated renal disorders.

Authors:  C Wehling; O Amon; M Bommer; B Hoppe; K Kentouche; G Schalk; R Weimer; M Wiesener; B Hohenstein; B Tönshoff; R Büscher; H Fehrenbach; Ö-N Gök; M Kirschfink
Journal:  Clin Exp Immunol       Date:  2016-11-25       Impact factor: 4.330

7.  Complement Factor C4d Is a Common Denominator in Thrombotic Microangiopathy.

Authors:  Jamie S Chua; Hans J Baelde; Malu Zandbergen; Suzanne Wilhelmus; Leendert A van Es; Johan W de Fijter; Jan A Bruijn; Ingeborg M Bajema; Danielle Cohen
Journal:  J Am Soc Nephrol       Date:  2015-01-08       Impact factor: 10.121

Review 8.  Complement in disease: a defence system turning offensive.

Authors:  Daniel Ricklin; Edimara S Reis; John D Lambris
Journal:  Nat Rev Nephrol       Date:  2016-05-23       Impact factor: 28.314

9.  Interventions for atypical haemolytic uraemic syndrome.

Authors:  Dan Pugh; Eoin D O'Sullivan; Fiona Ai Duthie; Philip Masson; David Kavanagh
Journal:  Cochrane Database Syst Rev       Date:  2021-03-23

10.  Severe active C3 glomerulonephritis triggered by immune complexes and inactivated after eculizumab therapy.

Authors:  Tanja Kersnik Levart; Dušan Ferluga; Alenka Vizjak; Jerica Mraz; Nika Kojc
Journal:  Diagn Pathol       Date:  2016-10-07       Impact factor: 2.644

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