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 …

The CXCL8/IL-8 chemokine family and its receptors in inflammatory diseases

RC Russo, CC Garcia, MM Teixeira… - Expert review of clinical …, 2014 - Taylor & Francis
Chemokines are small proteins that control several tissue functions, including cell
recruitment and activation under homeostatic and inflammatory conditions. CXCL8 …

Is there a crossroad between infections, genetics, and Henoch–Schönlein purpura?

D Rigante, L Castellazzi, A Bosco, S Esposito - Autoimmunity reviews, 2013 - Elsevier
Henoch–Schönlein purpura is the most common systemic vasculitis in childhood,
characterized by the presence of immunoglobulin A deposits in the small vessels of skin …

[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 …

Causal relationships between circulating inflammatory factors and IgA vasculitis: a bidirectional Mendelian randomization study

J Qin, L Zhang, B Ke, T Liu, C Kong, C Jin - Frontiers in Immunology, 2023 - frontiersin.org
Background IgA vasculitis (IgAV) is an immune-associated vasculitis, yet its exact etiology
remains unclear. Here, we explore the interaction between IgAV and inflammatory factors …

IgA vasculitis or Henoch-Schönlein purpura: genetics and beyond

M Jelusic, M Sestan - Pediatric Nephrology, 2021 - Springer
Considering the fact that the IgA vasculitis (IgAV), formerly known as Henoch-Schönlein
purpura, is the most common systemic vasculitis in childhood, with an incidence fluctuating …

Advances in our understanding of the pathogenesis of Henoch-Schönlein purpura and the implications for improving its diagnosis

SJ Park, JS Suh, JH Lee, JW Lee, SH Kim… - Expert Review of …, 2013 - Taylor & Francis
Henoch-Schönlein purpura (HSP) is a leukocytoclastic vasculitis classically characterized by
palpable purpura, arthritis, abdominal pain and renal disease. In this article, we summarize …

Polymorphism of the IL-8 gene and the risk of ovarian cancer

D Koensgen, D Bruennert, S Ungureanu, D Sofroni… - Cytokine, 2015 - Elsevier
Ovarian cancer still represents a challenge in gynecological oncology. Most patients are
diagnosed in an advanced tumor stage. No specific screening or prevention strategies for …

[HTML][HTML] IgA 血管炎免疫学发病机制的研究进展

刘雅婷, 卢思广 - 中国当代儿科杂志, 2017 - zgddek.com
IgA 血管炎(IgAV) 是儿童最常见的白细胞碎裂性小血管炎, 主要累及皮肤小血管, 关节,
消化道及肾脏, 其发病机制并不完全明确. 目前认为是在遗传的基础上, 受环境影响 …

Association of TLR4 gene polymorphisms with childhood Henoch–Schönlein purpura in a Chinese population

H Xu, G Jiang, H Shen, W Li, J Mao, Y Pan - Rheumatology International, 2017 - Springer
Recent studies demonstrated that aberrant activation of Toll-like receptor (TLR) 4 was
involved in the pathogenesis of Henoch–Schönlein purpura (HSP). In this study, we …