Modern challenges in infection prevention: encapsulated organisms in the era of novel complement inhibitors

Ayman Al Jurdi1, Camille N Kotton2, Richard Lafayette3

  • 1Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.

Kidney International
|December 27, 2025
PubMed

Insights

Complement inhibitors are approved for kidney diseases like atypical HUS and IgA nephropathy. This review guides nephrologists on preventing infections, especially from encapsulated organisms, when using these novel therapies.

Area of Science:

  • Nephrology
  • Immunology
  • Pharmacology

Background:

  • Complement inhibitors are increasingly approved for treating rare kidney diseases, including atypical hemolytic uremic syndrome (aHUS), IgA nephropathy, and C3 glomerulopathy.
  • These targeted therapies offer new treatment avenues for patients with specific glomerular diseases.
  • The expanding use of complement inhibitors necessitates a proactive approach to managing potential side effects.

Purpose of the Study:

  • To provide guidance for nephrologists on preventing infectious complications associated with complement inhibitor therapy.
  • To specifically address the risk of infections caused by encapsulated organisms in patients receiving complement inhibitors.
  • To support the safe and effective utilization of complement inhibitors in nephrology practice.

Main Methods:

  • This is a review article, synthesizing current literature and clinical guidelines.
  • It focuses on the pathophysiology of complement-mediated kidney diseases and the mechanism of action of complement inhibitors.
  • The review analyzes data on infection risks associated with immunosuppressive therapies in nephrology.

Main Results:

  • Complement inhibitors, while effective, increase the risk of serious infections, particularly from encapsulated bacteria (e.g., Streptococcus pneumoniae, Neisseria meningitidis, Haemophilus influenzae).
  • Prophylactic strategies, including vaccination and potentially antimicrobial prophylaxis, are crucial for mitigating these risks.
  • Understanding the specific complement pathway targeted by the inhibitor may inform risk stratification and management.

Conclusions:

  • Nephrologists must be vigilant in monitoring for and preventing infections in patients treated with complement inhibitors.
  • Implementing preventive measures, such as vaccination schedules and patient education, is essential for optimizing outcomes.
  • Further research is needed to refine prophylactic strategies and long-term safety profiles for complement inhibitor use in kidney disease.

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