A review of the mechanism of vascular endothelial injury in immunoglobulin a vasculitis

S Xu, S Han, Y Dai, L Wang, X Zhang… - Frontiers in Physiology, 2022 - frontiersin.org
Immunoglobulin A (IgA) vasculitis (IgAV), also known as Henoch-Schönlein purpura, is the
most common form of childhood vasculitis. It is characterized by cutaneous hemorrhage …

[HTML][HTML] New insights in the pathogenesis of immunoglobulin A vasculitis (Henoch-Schönlein purpura)

MH Heineke, AV Ballering, A Jamin, SB Mkaddem… - Autoimmunity …, 2017 - Elsevier
Immunoglobulin A vasculitis (IgAV), also referred to as Henoch-Schönlein purpura, is the
most common form of childhood vasculitis. The pathogenesis of IgAV is still largely …

[HTML][HTML] Pathogenesis of IgA vasculitis: an up-to-date review

Y Song, X Huang, G Yu, J Qiao, J Cheng, J Wu… - Frontiers in …, 2021 - frontiersin.org
Immunoglobin A (IgA) vasculitis (IgAV), formerly called the Henoch-Schönlein purpura
(HSP), is a small vessel vasculitis, characterized by IgA1-dominant immune deposition at …

[HTML][HTML] IgA vasculitis update: Epidemiology, pathogenesis, and biomarkers

L Xu, Y Li, X Wu - Frontiers in Immunology, 2022 - frontiersin.org
Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura, is the
most common systemic vasculitis in children, characterized by diverse clinical …

[HTML][HTML] Genetics of immunoglobulin-A vasculitis (Henoch-Schönlein purpura): An updated review

R López-Mejías, S Castañeda, F Genre… - Autoimmunity …, 2018 - Elsevier
Immunoglobulin-A vasculitis (IgAV) is classically a childhood small-sized blood vessel
vasculitis with predominant involvement of the skin. Gastrointestinal and joint manifestations …

Mechanisms of endothelial cell injury in vasculitis

AA Pall, COS Savage - Springer seminars in immunopathology, 1994 - Springer
The aetiology of the primary systemic vasculitides remains obscure. Recent years have seen
significant advances in our understanding of inflammation and in particular the role of and …

IgA vasculitis: etiology, treatment, biomarkers and epigenetic changes

H Sugino, Y Sawada, M Nakamura - International journal of molecular …, 2021 - mdpi.com
IgA, previously called Henoch-Schönlein vasculitis, is an essential immune component that
drives the host immune response to the external environment. As IgA has the unique …

[HTML][HTML] Childhood IgA vasculitis (Henoch Schonlein purpura)—advances and knowledge gaps

L Oni, S Sampath - Frontiers in pediatrics, 2019 - frontiersin.org
Immunoglobulin A vasculitis (IgAV; formerly Henoch Schonlein Purpura) is the most
common form of childhood vasculitis. It can occur in any age and peaks around 4–6 years …

[HTML][HTML] New insights and challenges associated with IgA vasculitis and IgA vasculitis with nephritis—is it time to change the paradigm of the most common systemic …

M Jelusic, M Sestan, T Giani, R Cimaz - Frontiers in pediatrics, 2022 - frontiersin.org
What are the challenges ahead and how have we responded so far when it comes to the
non-granulomatous systemic vasculitis, characterized mainly by deposits of IgA immune …

Multisystemic manifestations of IgA vasculitis

L Du, P Wang, C Liu, S Li, S Yue, Y Yang - Clinical Rheumatology, 2021 - Springer
Immunoglobulin A vasculitis (IgAV), also known as Henoch-Schönlein Purpura, is one of the
most common kind of systemic vasculitis in children, and due to the involvement of small …