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Artikel ; Online: Human inherited complete STAT2 deficiency underlies inflammatory viral diseases

Giorgia Bucciol / Leen Moens / Masato Ogishi / Darawan Rinchai / Daniela Matuozzo / Mana Momenilandi / Nacim Kerrouche / Catherine M. Cale / Elsa R. Treffeisen / Mohammad Al Salamah / Bandar K. Al-Saud / Alain Lachaux / Remi Duclaux-Loras / Marie Meignien / Aziz Bousfiha / Ibtihal Benhsaien / Anna Shcherbina / Anna Roppelt / COVID Human Genetic Effort /
Florian Gothe / Nadhira Houhou-Fidouh / Scott J. Hackett / Lisa M. Bartnikas / Michelle C. Maciag / Mohammed F. Alosaimi / Janet Chou / Reem W. Mohammed / Bishara J. Freij / Emmanuelle Jouanguy / Shen-Ying Zhang / Stephanie Boisson-Dupuis / Vivien Béziat / Qian Zhang / Christopher J.A. Duncan / Sophie Hambleton / Jean-Laurent Casanova / Isabelle Meyts

The Journal of Clinical Investigation, Vol 133, Iss

2023  Band 12

Abstract: STAT2 is a transcription factor activated by type I and III IFNs. We report 23 patients with loss-of-function variants causing autosomal recessive (AR) complete STAT2 deficiency. Both cells transfected with mutant STAT2 alleles and the patients’ cells ... ...

Abstract STAT2 is a transcription factor activated by type I and III IFNs. We report 23 patients with loss-of-function variants causing autosomal recessive (AR) complete STAT2 deficiency. Both cells transfected with mutant STAT2 alleles and the patients’ cells displayed impaired expression of IFN-stimulated genes and impaired control of in vitro viral infections. Clinical manifestations from early childhood onward included severe adverse reaction to live attenuated viral vaccines (LAV) and severe viral infections, particularly critical influenza pneumonia, critical COVID-19 pneumonia, and herpes simplex virus type 1 (HSV-1) encephalitis. The patients displayed various types of hyperinflammation, often triggered by viral infection or after LAV administration, which probably attested to unresolved viral infection in the absence of STAT2-dependent types I and III IFN immunity. Transcriptomic analysis revealed that circulating monocytes, neutrophils, and CD8+ memory T cells contributed to this inflammation. Several patients died from viral infection or heart failure during a febrile illness with no identified etiology. Notably, the highest mortality occurred during early childhood. These findings show that AR complete STAT2 deficiency underlay severe viral diseases and substantially impacts survival.
Schlagwörter Immunology ; Medicine ; R
Sprache Englisch
Erscheinungsdatum 2023-06-01T00:00:00Z
Verlag American Society for Clinical Investigation
Dokumenttyp Artikel ; Online
Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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