The role of inflammation in retinal neurodegeneration and degenerative diseases

G Kaur, NK Singh - International Journal of Molecular Sciences, 2021 - mdpi.com
Retinal neurodegeneration is predominantly reported as the apoptosis or impaired function
of the photoreceptors. Retinal degeneration is a major causative factor of irreversible vision …

The human factor H protein family–an update

N Sándor, AE Schneider, AT Matola… - Frontiers in …, 2024 - frontiersin.org
Complement is an ancient and complex network of the immune system and, as such, it plays
vital physiological roles, but it is also involved in numerous pathological processes. The …

Anti-factor H antibody and its role in atypical hemolytic uremic syndrome

R Raina, G Mangat, G Hong, R Shah, N Nair… - Frontiers in …, 2022 - frontiersin.org
Atypical hemolytic uremic syndrome (aHUS) an important form of a thrombotic
microangiopathy (TMA) that can frequently lead to acute kidney injury (AKI). An important …

Rare variants in complement gene in C3 glomerulopathy and immunoglobulin-mediated membranoproliferative GN

MS Meuleman, P Vieira-Martins… - Clinical Journal of the …, 2023 - journals.lww.com
Background C3 glomerulopathy and idiopathic immunoglobulin-mediated
membranoproliferative GN (Ig-MPGN) are rare complement-mediated kidney diseases …

Clinicopathologic implications of complement genetic variants in kidney transplantation

Z Ren, SJ Perkins, L Love-Gregory, JP Atkinson… - Frontiers in …, 2021 - frontiersin.org
Genetic testing has uncovered rare variants in complement proteins associated with
thrombotic microangiopathy (TMA) and C3 glomerulopathy (C3G). Approximately 50% are …

Atypical hemolytic uremic syndrome: diagnosis, management, and discontinuation of therapy

A Java - Hematology, 2024 - ashpublications.org
Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy typically
characterized by anemia, thrombocytopenia, and end-organ injury. aHUS occurs due to …

Rare germline complement factor H variants in patients with paroxysmal nocturnal hemoglobinuria

PH Prata, JE Galimard, F Sicre de Fontbrune, A Duval… - Blood, 2023 - ashpublications.org
Patients with paroxysmal nocturnal hemoglobinuria (PNH) are susceptible to complement-
mediated intravascular hemolysis and thrombosis. Factor H (FH) is the main regulator of the …

Adamts7-mediated complement factor H degradation potentiates complement activation to contributing to renal injuries

Z Ma, C Mao, Y Jia, F Yu, P Xu, Y Tan… - Journal of the …, 2023 - journals.lww.com
Background The dysfunction of complement factor H (CFH), the main soluble complement
negative regulator, potentiates various complement-induced renal injuries. However …

The role of properdin and Factor H in disease

C Cortes, C Desler, A Mazzoli, JY Chen… - Advances in …, 2022 - Elsevier
The complement system consists of three pathways (alternative, classical, and lectin) that
play a fundamental role in immunity and homeostasis. The multifunctional role of the …

[HTML][HTML] Atypical hemolytic uremic syndrome: genetically-based insights into pathogenesis through an analysis of the complement regulator CD46

X Wu, MK Liszewski, A Java, JP Atkinson - Annals of Blood, 2023 - aob.amegroups.org
The complement system is a critical innate immune defense mechanism that also facilitates
antigen recognition as well as antibody production through the adaptive immune response …