STAT proteins: a kaleidoscope of canonical and non-canonical functions in immunity and cancer
STAT proteins represent an important family of evolutionarily conserved transcription factors
that play key roles in diverse biological processes, notably including blood and immune cell …
that play key roles in diverse biological processes, notably including blood and immune cell …
Differentiating between UCTD and early-stage SLE: from definitions to clinical approach
S Sciascia, D Roccatello, M Radin, I Parodis… - Nature Reviews …, 2022 - nature.com
Systemic lupus erythematosus (SLE) is an autoimmune disease with heterogeneous clinical
manifestations that can potentially affect every organ and system. SLE is usually identified …
manifestations that can potentially affect every organ and system. SLE is usually identified …
Combined proteomics and single cell RNA-sequencing analysis to identify biomarkers of disease diagnosis and disease exacerbation for systemic lupus …
Y Li, C Ma, S Liao, S Qi, S Meng, W Cai, W Dai… - Frontiers in …, 2022 - frontiersin.org
Introduction Systemic lupus erythematosus (SLE) is a chronic autoimmune disease for which
there is no cure. Effective diagnosis and precise assessment of disease exacerbation …
there is no cure. Effective diagnosis and precise assessment of disease exacerbation …
[HTML][HTML] SARS-Cov2 acute and post-active infection in the context of autoimmune and chronic inflammatory diseases
R Larionova, K Byvaltsev, О Kravtsova, E Takha… - Journal of Translational …, 2022 - Elsevier
The clinical and immunological spectrum of acute and post-active COVID-19 syndrome
overlaps with criteria used to characterize autoimmune diseases such as rheumatoid …
overlaps with criteria used to characterize autoimmune diseases such as rheumatoid …
Identification of key interferon-stimulated genes for indicating the condition of patients with systemic lupus erythematosus
M Shen, C Duan, C Xie, H Wang, Z Li, B Li… - Frontiers in …, 2022 - frontiersin.org
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with highly
heterogeneous clinical symptoms and severity. There is complex pathogenesis of SLE, one …
heterogeneous clinical symptoms and severity. There is complex pathogenesis of SLE, one …
Placental damage in pregnancies with systemic lupus erythematosus: A narrative review
AS Castellanos Gutierrez, F Figueras… - Frontiers in …, 2022 - frontiersin.org
Systemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune disease of
unknown cause, which mainly affects women of childbearing age, especially between 15 …
unknown cause, which mainly affects women of childbearing age, especially between 15 …
The crucial regulatory role of type I interferon in inflammatory diseases
L Ji, T Li, H Chen, Y Yang, E Lu, J Liu, W Qiao, H Chen - Cell & Bioscience, 2023 - Springer
Abstract Type I interferon (IFN-I) plays crucial roles in the regulation of inflammation and it is
associated with various inflammatory diseases including systemic lupus erythematosus …
associated with various inflammatory diseases including systemic lupus erythematosus …
Interferons and systemic lupus erythematosus: Pathogenesis, clinical features, and treatments in interferon-driven disease
Y Tanaka, M Kusuda, Y Yamaguchi - Modern Rheumatology, 2023 - academic.oup.com
Type I interferons (IFNs) have recently received a lot of attention with the elucidation of the
pathogenesis of systemic lupus erythematosus (SLE). Type I IFNs are associated with many …
pathogenesis of systemic lupus erythematosus (SLE). Type I IFNs are associated with many …
Novel heterozygous TREX1 mutation in a juvenile systemic lupus erythematosus patient with severe cutaneous involvement treated successfully with Jak-inhibitors: a …
M Rossano, EA Conti, P Bocca, S Volpi… - Frontiers in …, 2023 - frontiersin.org
Juvenile systemic lupus erythematosus (jSLE) is a complex inflammatory autoimmune
disorder. In the last decades, genetic factors and activation pathways have been …
disorder. In the last decades, genetic factors and activation pathways have been …
Gene signature of regulatory T Cells isolated from children with selective IgA deficiency and common variable immunodeficiency
M Rutkowska-Zapała, A Grabowska-Gurgul, M Lenart… - Cells, 2024 - mdpi.com
Selective IgA deficiency (SIgAD) is the most common form and common variable
immunodeficiency (CVID) is the most symptomatic form of predominant antibody deficiency …
immunodeficiency (CVID) is the most symptomatic form of predominant antibody deficiency …