| Literature DB >> 32470544 |
Hannah Siedel1, Axel Roers2, Angela Rösen-Wolff3, Hella Luksch1.
Abstract
STING-associated vasculopathy with onset in infancy (SAVI) is an autoimmune disease caused by heterozygous gain of function mutations of STING (stimulator of interferon genes) that had initially been classified as a type I interferonopathy. We recently reported a genetically engineered mouse strain carrying a common SAVI-associated STING mutation. These STING N153S/WT mice reproduce key features of SAVI, including lung inflammation, loss of T cells in spleen and blood, splenomegaly and thymic hypoplasia. Here we show that αβ T lymphocytopenia is due to disrupted T cell development and is associated with impaired T cell activation and a relative increase in γδ T cell numbers. These alterations were not rescued by additional knockout of the type I IFN receptor (IFNAR1). Collectively, our findings consolidate the concept that constitutive STING signalling leads to a SCID-like phenotype in STING N153S/WT mice.Entities:
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Year: 2020 PMID: 32470544 DOI: 10.1016/j.clim.2020.108466
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969