C3 glomerulopathy—understanding a rare complement-driven renal disease

RJH Smith, GB Appel, AM Blom, HT Cook… - Nature reviews …, 2019 - nature.com
The C3 glomerulopathies are a group of rare kidney diseases characterized by complement
dysregulation occurring in the fluid phase and in the glomerular microenvironment, which …

The Factor H protein family: The switchers of the complement alternative pathway

L Lucientes‐Continente… - Immunological …, 2023 - Wiley Online Library
The factor H (FH) protein family is emerging as a complex network of proteins controlling the
fate of the complement alternative pathway (AP) and dictating susceptibility to a wide range …

[HTML][HTML] Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

A Servais, LH Noël, LT Roumenina, M Le Quintrec… - Kidney international, 2012 - Elsevier
Dense deposit disease and glomerulonephritis with isolated C3 deposits are
glomerulopathies characterized by deposits of C3 within or along the glomerular basement …

Complement C3 variant and the risk of age-related macular degeneration

JRW Yates, T Sepp, BK Matharu, JC Khan… - … England Journal of …, 2007 - Mass Medical Soc
Background Age-related macular degeneration is the most common cause of blindness in
Western populations. Susceptibility is influenced by age and by genetic and environmental …

Complement control protein factor H: the good, the bad, and the inadequate

VP Ferreira, MK Pangburn, C Cortés - Molecular immunology, 2010 - Elsevier
The complement system is an essential component of the innate immune system that
participates in elimination of pathogens and altered host cells and comprises an essential …

The human complement factor H: functional roles, genetic variations and disease associations

SR de Córdoba, J Esparza-Gordillo, EG de Jorge… - Molecular …, 2004 - Elsevier
Factor H is an essential regulatory protein that plays a critical role in the homeostasis of the
complement system in plasma and in the protection of bystander host cells and tissues from …

Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H

MC Pickering, HT Cook, J Warren, AE Bygrave… - Nature …, 2002 - nature.com
The alternative pathway of complement is activated continuously in vivo through the C3'tick-
over'pathway 1. This pathway is triggered by the hydrolysis of C3, resulting in the formation …

The central role of the alternative complement pathway in human disease

JM Thurman, VM Holers - The Journal of Immunology, 2006 - journals.aai.org
The complement system is increasingly recognized as important in the pathogenesis of
tissue injury in vivo following immune, ischemic, or infectious insults. Within the complement …

Systemic lupus erythematosus, complement deficiency, and apoptosis

MC Pickering, M Botto, PR Taylor, PJ Lachmann… - Advances in …, 2001 - Elsevier
There are many links between the complement system and the autoimmune disease
systemic lupus erythematosus (SLE). Soon after the identification of antinuclear antibodies …

Control of the complement system.

MK Liszewski, TC Farries, DM Lublin… - Advances in …, 1996 - europepmc.org
The complement system has developed a remarkably simple but elegant manner of
regulating itself. It has faced and successfully dealt with how to facilitate activation on a …