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Published on: September 5, 2016
Advances and challenges in the management of complement-mediated thrombotic microangiopathies
Jean-Claude Davin1, Nicole C A J van de Kar2
1Paediatric Nephrology Department, Emma Children's Hospital-Academic Medical Centre, Meibergdreef 9, 1105 AZ Amsterdam Z-O, The Netherlands.
Insights
Atypical hemolytic uremic syndrome (aHUS) is a severe kidney disease driven by complement activation. Anti-C5 monoclonal antibodies (anti-C5 mAb) are now first-line treatment, significantly improving outcomes despite high costs.
Area of Science:
- Nephrology
- Immunology
- Hematology
Background:
- Complement activation is central to renal pathophysiology, leading to inflammation and cell lysis.
- Atypical hemolytic uremic syndrome (aHUS) involves excessive complement activation in microcirculation, causing thrombotic microangiopathy.
- Untreated aHUS leads to end-stage renal failure or death in over 50% of patients.
Purpose of the Study:
- To review the advancements in understanding and treating atypical hemolytic uremic syndrome (aHUS).
- To highlight the pivotal role of complement inhibitors, specifically anti-C5 monoclonal antibodies (anti-C5 mAb), in managing aHUS.
- To discuss the current treatment landscape and future directions for aHUS therapy.
Main Methods:
- Review of scientific literature on complement activation in renal diseases and aHUS.
- Analysis of treatment protocols including plasma therapy, transplantation, and complement inhibition.
- Evaluation of the efficacy and limitations of anti-C5 mAb in aHUS management.
Main Results:
- Significant progress in understanding aHUS etiology has led to improved therapeutic strategies.
- Plasma therapy and transplantation were established treatments, with anti-C5 mAb emerging as first-line therapy.
- Anti-C5 mAb demonstrates favorable effects in aHUS, though high cost limits global accessibility.
Conclusions:
- Complement inhibition, particularly with anti-C5 mAb, represents a major therapeutic advance for aHUS.
- Vaccination against meningococcal infection is crucial before initiating anti-C5 mAb therapy.
- Future efforts should focus on reducing costs through generics and developing alternative complement inhibitors to improve worldwide access.
Abstract:
Complement activation plays a major role in several renal pathophysiological conditions. The three pathways of complement lead to C3 activation, followed by the formation of the anaphylatoxin C5a and the terminal membrane attack complex (MAC) in blood and at complement activating surfaces, lead to a cascade of events responsible for inflammation and for the induction of cell lysis. In case of ongoing uncontrolled complement activation, endothelial cells activation takes place, leading to events in which at the end thrombotic microangiopathy can occur. Atypical haemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy characterized by excessive complement activation on the surface of the microcirculation. It is a severe, rare disease which leads to end-stage renal failure (ESRF) and/or to death in more than 50% of patients without treatment. In the first decade of the second millennium, huge progress in understanding the aetiology of this disease was made, which paved the way to better treatment. First, protocols of plasma therapy for treatment, prevention of relapses and for renal transplantation in those patients were set up. Secondly, in some severe cases, combined kidney and liver transplantation was reported. Finally, at the end of this decade, the era of complement inhibitors, as anti-C5 monoclonal antibody (anti-C5 mAb) began. The past five years have seen growing evidence of the favourable effect of anti-C5 mAb in aHUS which has made this drug the first-line treatment in this disease. The possible complication of meningococcal infection needs appropriate vaccination before its use. Unfortunately, the worldwide use of anti-C5 mAb is limited by its very high price. In the future, extension of indications for anti-C5 mAb use, the elaboration of generics and of mAbs directed towards other complement factors of the terminal pathway of the complement system might succeed in reducing the cost of this new valuable therapeutic approach and render it available worldwide for patients from all social classes.
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