Spotlight: “Human STAT2 deficiency: a severe defect of antiviral immunity”
Author:
Funder
KU Leuven
Jeffrey Modell Foundation
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics,Immunology
Link
https://www.nature.com/articles/s41435-023-00246-3.pdf
Reference9 articles.
1. Duncan CJA, Hambleton S. Human disease phenotypes associated with loss and gain of function mutations in STAT2: viral susceptibility and type I interferonopathy. J Clin Immunol. 2021;41:1446–56.
2. Meyts I, Casanova JL. Viral infections in humans and mice with genetic deficiencies of the type I IFN response pathway. Eur J Immunol. 2021;51:1039–61.
3. Bucciol G, Moens L, Ogishi M, Rinchai D, Matuozzo D, Momenilandi M, et al. Human inherited complete STAT2 deficiency underlies inflammatory viral diseases. J Clin Invest. 2023;133:e168321.
4. Zhang Q, Matuozzo D, Le Pen J, Lee D, Moens L, Asano T, et al. Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia. J Exp Med. 2022;219:e20220131.
5. López-Nevado M, Sevilla J, Almendro-Vázquez P, Gil-Etayo FJ, Garcinuño S, Serrano-Hernández A, et al. Inborn error of STAT2-dependent IFN-I immunity in a patient presented with hemophagocytic lymphohistiocytosis and multisystem inflammatory syndrome in children. J Clin Immunol. 2023;43:1278–88.
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