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Alliance"],"published-print":{"date-parts":[[2019,6]]},"abstract":"<jats:p>STING-associated vasculopathy with onset in infancy (SAVI) is an autoinflammatory disorder characterized by blood vessel occlusions, acral necrosis, myositis, rashes, and pulmonary inflammation that are the result of activating mutations in the STimulator of Interferon Genes (STING). We generated a transgenic line that recapitulates many of the phenotypic aspects of SAVI by targeting the expression of the human STING-N154S\u2013mutant protein to the murine hematopoietic compartment.<jats:italic>hSTING-N154S<\/jats:italic>mice demonstrated failure to gain weight, lymphopenia, progressive paw swelling accompanied by inflammatory infiltrates, severe myositis, and ear and tail necrosis. However, no significant lung inflammation was observed. X-ray microscopy imaging revealed vasculopathy characterized by arteriole occlusions and venous thromboses. Type I interferons and proinflammatory mediators were elevated in<jats:italic>hSTING-N154S<\/jats:italic>sera. Importantly, the phenotype was prevented in<jats:italic>hSTING-N154S<\/jats:italic>mice lacking the type I interferon receptor gene (<jats:italic>Ifnar1<\/jats:italic>). This model, based on a mutant human STING protein, may shed light on the pathophysiological mechanisms operative in SAVI.<\/jats:p>","DOI":"10.26508\/lsa.201800215","type":"journal-article","created":{"date-parts":[[2019,6,20]],"date-time":"2019-06-20T18:55:15Z","timestamp":1561056915000},"page":"e201800215","update-policy":"https:\/\/doi.org\/10.26508\/lsa.crossmarkpolicy","source":"Crossref","is-referenced-by-count":34,"title":["Expression of a constitutively active human<i>STING<\/i>mutant in hematopoietic cells produces an<i>Ifnar1<\/i>-dependent vasculopathy in mice"],"prefix":"10.26508","volume":"2","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8237-5436","authenticated-orcid":true,"given":"Gary R","family":"Martin","sequence":"first","affiliation":[{"name":"Department of Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, Canada"},{"name":"The McCaig Institute for Bone and Joint Health, Cumming School of Medicine, University of 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