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<title>Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children</title>
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<description>Multisystem inflammatory syndrome in children (MIS-C) is a rare and severe condition that follows benign COVID-19. We report autosomal recessive deficiencies of OAS1, OAS2, or RNASEL in five unrelated children with MIS-C. The cytosolic double-stranded RNA (dsRNA)–sensing OAS1 and OAS2 generate 2′-5′-linked oligoadenylates (2-5A) that activate the single-stranded RNA–degrading ribonuclease L (RNase L). Monocytic cell lines and primary myeloid cells with OAS1, OAS2, or RNase L deficiencies produce excessive amounts of inflammatory cytokines upon dsRNA or severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) stimulation. Exogenous 2-5A suppresses cytokine production in OAS1-deficient but not RNase L–deficient cells. Cytokine production in RNase L–deficient cells is impaired by MDA5 or RIG-I deficiency and abolished by mitochondrial antiviral-signaling protein (MAVS) deficiency. Recessive OAS–RNase L deficiencies in these patients unleash the production of SARS-CoV-2–triggered, MAVS-mediated inflammatory cytokines by mononuclear phagocytes, thereby underlying MIS-C.</description>
<date>2025-01-24</date>
<date>2025-01-24</date>
<date>2023-02</date>
<type>info:eu-repo/semantics/article</type>
<identifier>0036-8075</identifier>
<identifier>http://hdl.handle.net/10259/10036</identifier>
<identifier>10.1126/SCIENCE.ABO3627</identifier>
<identifier>1095-9203</identifier>
<language>eng</language>
<relation>Science. 2023, V. 379, n. 6632</relation>
<relation>https://doi.org/10.1126/science.abo3627</relation>
<rights>http://creativecommons.org/licenses/by/4.0/</rights>
<rights>info:eu-repo/semantics/openAccess</rights>
<rights>Atribución 4.0 Internacional</rights>
<publisher>American Association for the Advancement of Science</publisher>
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