Dermatomyositis: clinical features and pathogenesis

ME DeWane, R Waldman, J Lu - Journal of the American Academy of …, 2020 - Elsevier
Dermatomyositis (DM) is an idiopathic inflammatory myopathy that is clinically
heterogeneous and that can be difficult to diagnose. Cutaneous manifestations sometimes …

PTPN22: the archetypal non-HLA autoimmunity gene

SM Stanford, N Bottini - Nature Reviews Rheumatology, 2014 - nature.com
PTPN22 encodes a tyrosine phosphatase that is expressed by haematopoietic cells and
functions as a key regulator of immune homeostasis by inhibiting T-cell receptor signalling …

239th ENMC international workshop: classification of dermatomyositis, Amsterdam, the Netherlands, 14–16 December 2018

AL Mammen, Y Allenbach, W Stenzel… - Neuromuscular …, 2020 - Elsevier
Idiopathic inflammatory myopathies (IIM) are a heterogenous family of diseases that can
affect the muscles, skin, lungs, and joints. There have been prior attempts to classify IIMs …

Early components of the complement classical activation pathway in human systemic autoimmune diseases

KE Lintner, YL Wu, Y Yang, CH Spencer… - Frontiers in …, 2016 - frontiersin.org
The complement system consists of effector proteins, regulators, and receptors that
participate in host defense against pathogens. Activation of the complement system, via the …

Risk factors and disease mechanisms in myositis

FW Miller, JA Lamb, J Schmidt… - Nature Reviews …, 2018 - nature.com
Autoimmune diseases develop as a result of chronic inflammation owing to interactions
between genes and the environment. However, the mechanisms by which autoimmune …

Complement in autoimmune diseases

P Vignesh, A Rawat, M Sharma, S Singh - Clinica Chimica Acta, 2017 - Elsevier
The complement system is an ancient and evolutionary conserved element of the innate
immune mechanism. It comprises of more than 20 serum proteins most of which are …

Sex differences in pediatric rheumatology

M Cattalini, M Soliani, MC Caparello… - Clinical reviews in allergy & …, 2019 - Springer
Autoimmune diseases affect up to 10% of the world's population and, as a whole, they are
far more common in females, although differences exist according to the single disease and …

Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic …

S Rothwell, RG Cooper, IE Lundberg… - Annals of the …, 2016 - ard.bmj.com
Objectives The idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of rare
autoimmune diseases characterised by muscle weakness and extramuscular manifestations …

The juvenile idiopathic inflammatory myopathies: pathogenesis, clinical and autoantibody phenotypes, and outcomes

LG Rider, K Nistala - Journal of internal medicine, 2016 - Wiley Online Library
The aim of this review was to summarize recent advances in the understanding of the
clinical and autoantibody phenotypes, their associated outcomes and the pathogenesis of …

Anti-MDA5 antibody-positive dermatomyositis: pathogenesis and clinical progress

X Lu, Q Peng, G Wang - Nature Reviews Rheumatology, 2024 - nature.com
Anti-melanoma differentiation-associated protein 5 (MDA5) antibody-positive
dermatomyositis (MDA5-DM) is a subtype of dermatomyositis. Although the aetiology and …