Whole blood transcriptome identifies interferon-regulated genes as key drivers in thrombotic primary antiphospholipid syndrome

KM Verrou, PP Sfikakis, MG Tektonidou - Journal of Autoimmunity, 2023 - Elsevier
Objective Pathogenesis of antiphospholipid syndrome (APS) isn't fully elucidated. We aimed
to identify gene signatures characterizing thrombotic primary APS (thrPAPS) and subgroups …

Trophoblast cell function in the antiphospholipid syndrome

S Vrzić Petronijević, A Vilotić, Ž Bojić-Trbojević… - Biomedicines, 2023 - mdpi.com
Antiphospholipid syndrome (APS) is a complex thrombo-inflammatory autoimmune disease
characterized by the presence of antiphospholipid antibodies (aPL). Women with APS are at …

Regulation of IFNβ expression: focusing on the role of its promoter and transcription regulators

J Fan, Q Li, J Liang, Z Chen, L Chen, J Lai… - Frontiers in …, 2023 - frontiersin.org
IFNβ is a single-copy gene without an intron. Under normal circumstances, it shows low or
no expression in cells. It is upregulated only when the body needs it or is stimulated. Stimuli …

[HTML][HTML] Системная красная волчанка и антифосфолипидный синдром: вчера, сегодня, завтра

ЕЛ Насонов, ТМ Решетняк, СК Соловьев… - Терапевтический …, 2023 - cyberleninka.ru
Иммуновоспалительные (аутоиммунные и аутовоспалительные) ревматические
заболевания-не только весьма распространенные и тяжелые хронические …

H3K4me3‐Mediated FOXJ2/SLAMF8 Axis Aggravates Thrombosis and Inflammation in β2GPI/Anti‐β2GPI‐Treated Monocytes

Y Tan, J Qiao, S Yang, H Liu, Q Wang, Q Liu… - Advanced …, 2024 - Wiley Online Library
Antiphospholipid syndrome (APS) is characterized by thrombus formation, poor pregnancy
outcomes, and a proinflammatory response. H3K4me3‐related monocytes activation are key …

Case Report: A case of recurrent thrombosis in pediatric antiphospholipid syndrome associated with pediatric onset systemic lupus

L Liu, L Liu, L Zhang, P Huang, X Dang, L Shuai… - Frontiers in …, 2023 - frontiersin.org
Systemic lupus erythematosus (SLE) is an autoimmune disease with multi-system
involvement as the main manifestation, and has complex and diverse clinical features …

ARID5B‐mediated LINC01128 epigenetically activated pyroptosis and apoptosis by promoting the formation of the BTF3/STAT3 complex in β2GPI/anti‐β2GPI‐treated …

Y Tan, J Qiao, S Yang, Q Wang, H Liu… - Clinical and …, 2024 - Wiley Online Library
Background Alterations of the trimethylation of histone 3 lysine 4 (H3K4me3) mark in
monocytes are implicated in the development of autoimmune diseases. Therefore, the …

[HTML][HTML] Primary and secondary antiphospholipid syndrome characteristics in an Egyptian cohort

CS Morad, D Fayez, M Mahmoud, FM Aboud - The Egyptian …, 2022 - Elsevier
Aim of the work To describe the clinical and laboratory characteristics of patients with
primary and secondary antiphospholipid syndrome (APS) in an Egyptian cohort. Patients …

Interaction between long noncoding RNAs and syncytin-1/syncytin-2 genes and transcripts: how noncoding RNAs may affect pregnancy in patients with systemic …

R Talotta - International Journal of Molecular Sciences, 2023 - mdpi.com
Background: Patients with systemic lupus erythematosus (SLE) often suffer from obstetric
complications not necessarily associated with the antiphospholipid syndrome. These events …

Systemic lupus erythematosus and antiphospholipid syndrome: past, present, future

EL Nasonov, TM Reshetnyak, SK Solovyev… - Terapevticheskii …, 2023 - ter-arkhiv.ru
Immune-inflammatory (autoimmune and autoinflammatory) rheumatic diseases are
widespread severe chronic inflammatory diseases and also “models” for studying the …