Journal article
Outcomes from the International Society of Nephrology Forum on Complement Therapeutics in C3G & IgAN
Kidney international
08/26/2026
DOI: 10.1016/j.kint.2026.08.007
PMID: 42648401
Abstract
C3 glomerulopathy (C3G) and primary immune-complex membranoproliferative glomerulonephritis (IC-MPGN) are both prototypical complement disorders in which complement overactivation is the primary driver of disease. Complement is not the primary cause of disease in IgA nephropathy (IgAN); however, increasing evidence implicates complement as a secondary factor in kidney damage in this more complex, multifactorial disorder. The success of recent clinical trials using alternative pathway complement inhibitors in C3G, IC-MPGN, and IgAN pose questions as to how they should be used in the real world. We report the findings of the 2025 International Society of Nephrology Forum on Complement Therapeutics in C3G & IgAN, where a global panel of experts considered the current state of knowledge, identified areas of uncertainty, and proposed optimal solutions. Areas of uncertainty and areas for future research included how complement biomarkers, complement autoantibodies, genetics and the kidney biopsy guide therapy. The current rationale for the use of complement inhibitors and their place within the current therapeutic landscape are discussed.
Details
- Title: Subtitle
- Outcomes from the International Society of Nephrology Forum on Complement Therapeutics in C3G & IgAN
- Creators
- D Kavanagh - Royal Victoria InfirmaryA Alladin-Karan - University of CalgaryS Alexander - Christian Medical College, VelloreS Chauvet - Hôpital Européen Georges-PompidouC K Cheung - University Hospitals of Leicester NHS TrustH T Cook - Imperial College Healthcare NHS TrustF Fakhouri - University of LausanneV Fremeaux-Bacchi - Hôpital EuropéenD P Gale - University College LondonP Garred - Copenhagen University HospitalR A Lafayette - Stanford UniversityA L T Ma - University of Hong KongC Nester - University of Iowa Stead Family Children’s HospitalR J H Smith - University of Iowa, Iowa Neuroscience InstituteE Pillebout - InsermH N Reich - University Health NetworkD V Rizk - University of Alabama at BirminghamI S D Roberts - John Radcliffe HospitalB H Rovin - The Ohio State University Wexner Medical CenterS H Sacks - King's College LondonS Shah - King's College LondonH Trimarchi - Hospital Británico de Buenos AiresM Vivarelli - Bambino Gesù Children's HospitalE K S Wong - Royal Victoria InfirmaryH Zhang - Peking UniversityJ Barratt - University of LeicesterForum Participants
- Resource Type
- Journal article
- Publication Details
- Kidney international
- DOI
- 10.1016/j.kint.2026.08.007
- PMID
- 42648401
- ISSN
- 1523-1755
- eISSN
- 1523-1755
- Publisher
- Elsevier
- Language
- English
- Electronic publication date
- 08/26/2026
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Nephrology, Dialysis and Transplantation; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
- Record Identifier
- 9985220839802771
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