Haemolytic uraemic syndrome

M Michael, A Bagga, SE Sartain, RJH Smith - The Lancet, 2022 - thelancet.com
Haemolytic uraemic syndrome (HUS) is a heterogeneous group of diseases that result in a
common pathology, thrombotic microangiopathy, which is classically characterised by the …

Coagulopathy in COVID-19: Focus on vascular thrombotic events

W Shi, J Lv, L Lin - Journal of molecular and cellular cardiology, 2020 - Elsevier
SARS-CoV-2 causes a phenotype of pneumonia with diverse manifestation, which is termed
as coronavirus disease 2019 (COVID-19). An impressive high transmission rate allows …

Terminal complement inhibitor ravulizumab in generalized myasthenia gravis

T Vu, A Meisel, R Mantegazza, D Annane… - NEJM …, 2022 - evidence.nejm.org
Background Generalized myasthenia gravis (gMG) is a rare, chronic, and debilitating
autoimmune disease. Activation of the complement system by autoantibodies against the …

Long-term efficacy and safety of ravulizumab in adults with anti-acetylcholine receptor antibody-positive generalized myasthenia gravis: results from the phase 3 …

A Meisel, D Annane, T Vu, R Mantegazza… - Journal of …, 2023 - Springer
Introduction Ravulizumab demonstrated efficacy and an acceptable safety profile versus
placebo in the randomized controlled period (RCP) of the phase 3 CHAMPION MG trial in …

Advances in understanding of pathogenesis and treatment of immune-mediated kidney disease: A review

S Kant, A Kronbichler, P Sharma, D Geetha - American Journal of Kidney …, 2022 - Elsevier
There continues to be rapid advancement in our understanding of the pathogenesis of
immune-mediated kidney disease. This progress has culminated in the development of …

Ravulizumab pharmacokinetics and pharmacodynamics in patients with generalized myasthenia gravis

T Vu, S Ortiz, M Katsuno, D Annane, R Mantegazza… - Journal of …, 2023 - Springer
Introduction The terminal complement C5 inhibitor ravulizumab has a long elimination half-
life, allowing maintenance dosing every 8 weeks. In the 26-week, double-blind, randomized …

Complement-mediated kidney diseases

F Poppelaars, JM Thurman - Molecular Immunology, 2020 - Elsevier
It has long been known that the complement cascade is activated in various forms of
glomerulonephritis. In many of these diseases, immune-complexes deposit in the glomeruli …

How I diagnose and treat atypical hemolytic uremic syndrome

F Fakhouri, N Schwotzer… - Blood, The Journal of …, 2023 - ashpublications.org
Our understanding and management of atypical hemolytic uremic syndrome (aHUS) have
dramatically improved in the last decade. aHUS has been established as a prototypic …

The role of complement in kidney disease

V Petr, JM Thurman - Nature Reviews Nephrology, 2023 - nature.com
The complement cascade comprises soluble and cell surface proteins and is an important
arm of the innate immune system. Once activated, the complement system rapidly generates …

[HTML][HTML] The long-acting C5 inhibitor, ravulizumab, is effective and safe in pediatric patients with atypical hemolytic uremic syndrome naïve to complement inhibitor …

G Ariceta, BP Dixon, SH Kim, G Kapur, T Mauch… - Kidney international, 2021 - Elsevier
Ravulizumab, a long-acting complement C5 inhibitor engineered from eculizumab, allows
extending maintenance dosing from every 2–3 weeks to every 4–8 weeks depending on …