C3‐dependent effector functions of complement

A Zarantonello, M Revel, A Grunenwald… - Immunological …, 2023 - Wiley Online Library
C3 is the central effector molecule of the complement system, mediating its multiple
functions through different binding sites and their corresponding receptors. We will introduce …

[HTML][HTML] Complement regulates nutrient influx and metabolic reprogramming during Th1 cell responses

M Kolev, S Dimeloe, G Le Friec, A Navarini, G Arbore… - Immunity, 2015 - cell.com
Expansion and acquisition of Th1 cell effector function requires metabolic reprogramming;
however, the signals instructing these adaptations remain poorly defined. Here we found …

[HTML][HTML] Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome

M Le Quintrec, J Zuber, B Moulin, N Kamar… - American Journal of …, 2013 - Elsevier
Atypical hemolytic and uremic syndrome (aHUS) is a severe disease strongly associated
with genetic abnormalities in the complement alternative pathway. In renal …

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome

AL Sellier-Leclerc, V Fremeaux-Bacchi… - Journal of the …, 2007 - journals.lww.com
Mutations in factor H (CFH), factor I (IF), and membrane cofactor protein (MCP) genes have
been described as risk factors for atypical hemolytic uremic syndrome (aHUS). This study …

Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome

F Bu, T Maga, NC Meyer, K Wang… - Journal of the …, 2014 - journals.lww.com
Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy caused by
uncontrolled activation of the alternative pathway of complement at the cell surface level that …

Mutations in complement regulatory proteins predispose to preeclampsia: a genetic analysis of the PROMISSE cohort

JE Salmon, C Heuser, M Triebwasser… - PLoS …, 2011 - journals.plos.org
Background Pregnancy in women with systemic lupus erythematosus (SLE) or
antiphospholipid antibodies (APL Ab)—autoimmune conditions characterized by …

Genetic variability shapes the alternative pathway complement activity and predisposition to complement‐related diseases

S Rodríguez de Córdoba - Immunological Reviews, 2023 - Wiley Online Library
The implementation of next‐generation sequencing technologies has provided a sharp
picture of the genetic variability in the components and regulators of the alternative pathway …

Hemolytic uremic syndrome in pregnancy and postpartum

A Bruel, D Kavanagh, M Noris, Y Delmas… - Clinical Journal of the …, 2017 - journals.lww.com
Background Pregnancy is associated with various forms of thrombotic microangiopathy,
including hemolytic uremic syndrome. A previous small French study suggested that …

New insights into postrenal transplant hemolytic uremic syndrome

J Zuber, M Le Quintrec, R Sberro-Soussan… - Nature Reviews …, 2011 - nature.com
After renal transplantation, hemolytic uremic syndrome (HUS) may occur either as a
recurrent or de novo form. Over the past decade, much effort has been devoted to …

The CD46-Jagged1 interaction is critical for human TH1 immunity

G Le Friec, D Sheppard, P Whiteman, CM Karsten… - Nature …, 2012 - nature.com
CD46 is a complement regulator with important roles related to the immune response. CD46
functions as a pathogen receptor and is a potent costimulator for the induction of interferon-γ …