[HTML][HTML] The interferon in idiopathic inflammatory myopathies: Different signatures and new therapeutic perspectives. A literature review
M Gasparotto, C Franco, E Zanatta, A Ghirardello… - Autoimmunity …, 2023 - Elsevier
Idiopathic inflammatory myopathies (IIM), even though sharing common clinical
manifestations, are characterized by diversified molecular pathogenetic mechanisms which …
manifestations, are characterized by diversified molecular pathogenetic mechanisms which …
Emerging treatment for Sjögren's disease: A review of recent phase II and III trials
RI Fox, CM Fox, SS McCoy - Expert Opinion on Emerging Drugs, 2023 - Taylor & Francis
Introduction Sjögren's Disease, SjD, is a systemic autoimmune disorder characterized by
reduced function of the salivary and lacrimal glands. Patients suffer from dryness, fatigue …
reduced function of the salivary and lacrimal glands. Patients suffer from dryness, fatigue …
[HTML][HTML] Type I interferon score is associated with the severity and poor prognosis in anti-MDA5 antibody-positive dermatomyositis patients
J Qian, R Li, Z Chen, Z Cao, L Lu, Q Fu - Frontiers in Immunology, 2023 - frontiersin.org
Objectives To investigate the clinical significance of the interferon (IFN) score, especially the
IFN-I score, in patients with anti-melanoma differentiation-associated gene 5 (MDA5) …
IFN-I score, in patients with anti-melanoma differentiation-associated gene 5 (MDA5) …
[PDF][PDF] Association of combined anti-ro52/TRIM21 and anti-ro60/SSA antibodies with increased sjögren disease severity through interferon pathway activation
E Bettacchioli, A Saraux, A Tison… - Arthritis & …, 2024 - publicatio.bibl.u-szeged.hu
The biologic diagnosis of primary Sjögren disease (SjD) mainly relies on anti-Ro60/SSA
antibodies, whereas the significance of anti-Ro52/TRIM21 antibodies currently remains …
antibodies, whereas the significance of anti-Ro52/TRIM21 antibodies currently remains …
[HTML][HTML] Type-I interferon pathway and DNA damage accumulation in peripheral blood of patients with psoriatic arthritis
GE Fragoulis, PA Ntouros, A Nezos… - Frontiers in …, 2023 - frontiersin.org
Objectives The abnormal DNA damage response is associated with upregulation of the type-
1 interferon (IFN-I) pathway in certain rheumatic diseases. We investigated whether such …
1 interferon (IFN-I) pathway in certain rheumatic diseases. We investigated whether such …
[HTML][HTML] Involvement of CCL2 in Salivary Gland Response to Hyperosmolar Stress Related to Sjögren's Syndrome
C Chivasso, D Parisis, X Cabrol, A Datlibagi… - International journal of …, 2024 - mdpi.com
In primary Sjögren's syndrome (pSS) patients, salivary gland (SG) epithelial cells (SGECs)
could be exposed to chronic hyperosmotic stress (HOS), consecutive to their destruction and …
could be exposed to chronic hyperosmotic stress (HOS), consecutive to their destruction and …
[HTML][HTML] Immunogenetics of Systemic Sclerosis
O Gumkowska-Sroka, K Kotyla, P Kotyla - Genes, 2024 - mdpi.com
Systemic sclerosis (SSc) is a rare autoimmune connective tissue disorder characterized by
massive fibrosis, vascular damage, and immune imbalance. Advances in rheumatology and …
massive fibrosis, vascular damage, and immune imbalance. Advances in rheumatology and …
An interactive web application for exploring systemic lupus erythematosus blood transcriptomic diversity
In the field of complex autoimmune diseases such as systemic lupus erythematosus (SLE),
systems immunology approaches have proven invaluable in translational research settings …
systems immunology approaches have proven invaluable in translational research settings …
Towards adaptive structuring of the lupologist's consultation to transform the care pathway of systemic lupus erythematosus
L Chiche, G Thomas, N Jourde-Chiche… - Medical Research …, 2023 - esmed.org
Systemic lupus erythematosus (SLE) is a complex autoimmune disease, which can be
clinically heterogeneous in the same patient over the disease process and has an …
clinically heterogeneous in the same patient over the disease process and has an …
Monogenic mimics of Behçet's Disease
AG Burleigh - 2023 - discovery.ucl.ac.uk
Behçet's Disease (BD) is a rare multisystemic variable vessel vasculitis with a chronic and
relapsing disease course. BD is polygenic, and genome wide association studies in cohorts …
relapsing disease course. BD is polygenic, and genome wide association studies in cohorts …