[HTML][HTML] Circular RNAs in immune responses and immune diseases

X Chen, T Yang, W Wang, W Xi, T Zhang, Q Li… - Theranostics, 2019 - ncbi.nlm.nih.gov
Circular RNAs (circRNAs) are novel clusters of endogenous noncoding RNAs (ncRNAs) that
are widely expressed in eukaryotic cells. In contrast to the generation of linear RNA …

Altered B cell signalling in autoimmunity

DJ Rawlings, G Metzler, M Wray-Dutra… - Nature reviews …, 2017 - nature.com
Recent work has provided new insights into how altered B cell-intrinsic signals—through the
B cell receptor (BCR) and key co-receptors—function together to promote the pathogenesis …

Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott–Aldrich syndrome

A Magnani, M Semeraro, F Adam, C Booth, L Dupré… - Nature Medicine, 2022 - nature.com
Abstract Patients with Wiskott–Aldrich syndrome (WAS) lacking a human leukocyte antigen-
matched donor may benefit from gene therapy through the provision of gene-corrected …

A map of human circular RNAs in clinically relevant tissues

PG Maass, P Glažar, S Memczak, G Dittmar… - Journal of molecular …, 2017 - Springer
Cellular circular RNAs (circRNAs) are generated by head-to-tail splicing and are present in
all multicellular organisms studied so far. Recently, circRNAs have emerged as a large class …

Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 …

F Ferrua, MP Cicalese, S Galimberti… - The Lancet …, 2019 - thelancet.com
Summary Background Wiskott-Aldrich syndrome is a rare, life-threatening, X-linked primary
immunodeficiency characterised by microthrombocytopenia, infections, eczema …

Clinical manifestations and pathophysiological mechanisms of the Wiskott-Aldrich syndrome

F Candotti - Journal of clinical immunology, 2018 - Springer
Abstract The Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder originally described
by Dr. Alfred Wiskott in 1937 and Dr. Robert Aldrich in 1954 as a familial disease …

RHO GTPases: from new partners to complex immune syndromes

R El Masri, J Delon - Nature Reviews Immunology, 2021 - nature.com
Ras homology (RHO) GTPases are signalling proteins that have crucial roles in triggering
multiple immune functions. Through their interactions with a broad range of effectors and …

Hereditary thrombocytopenias: a growing list of disorders

P Noris, A Pecci - Hematology 2014, the American Society of …, 2017 - ashpublications.org
The introduction of high throughput sequencing (HTS) techniques greatly improved the
knowledge of inherited thrombocytopenias (ITs) over the last few years. A total of 33 different …

FOXP3 deficiency, from the mechanisms of the disease to curative strategies

S Borna, E Meffre, R Bacchetta - Immunological Reviews, 2024 - Wiley Online Library
FOXP3 gene is a key transcription factor driving immune tolerance and its deficiency causes
immune dysregulation, polyendocrinopathy, enteropathy X‐linked syndrome (IPEX), a …

AIRE expression controls the peripheral selection of autoreactive B cells

J Sng, B Ayoglu, JW Chen, JN Schickel… - Science …, 2019 - science.org
Autoimmune regulator (AIRE) mutations result in autoimmune polyendocrinopathy-
candidiasis-ectodermal dystrophy (APECED) syndrome characterized by defective central T …