Fatal COVID-19 Infection in Two Children with STAT1 Gain-of-Function

• Published in: Journal of clinical immunology 2024-01, Vol.44 (1), p.20-20, Article 20
• Main Authors: Staines-Boone, Aidé Tamara, Vignesh, Pandiarajan, Tsumura, Miyuki, de la Garza Fernández, Germán, Tyagi, Reva, Rawat, Amit, Das, Jhumki, Tomomasa, Dan, Asano, Takaki, Hijikata, Atsushi, Salazar-Gálvez, Yuridia, Kanegane, Hirokazu, Okada, Satoshi, Reyes, Saul O Lugo
• Format: Article
• Language: English
• Subjects: Biomedical and Life Sciences; Biomedicine; Child; Child, Preschool; Cough; COVID-19; COVID-19 - genetics; Gain of Function Mutation; Histiocytosis; Humans; Hypoxemia; Immunology; Immunoregulation; Infections; Infectious Diseases; Interferon; Interferon Type I; Interferon-alpha - genetics; Internal Medicine; Lymphocytosis; Medical Microbiology; Myxovirus resistance proteins; Original Article; Patients; Regulatory sequences; SARS-CoV-2 - metabolism; Severe acute respiratory syndrome coronavirus 2; Stat1 protein; STAT1 Transcription Factor - genetics; STAT1 Transcription Factor - metabolism; α-Interferon; γ-Interferon
• ISSN: 0271-9142; 1573-2592
• DOI: 10.1007/s10875-023-01634-0

While SARS-CoV-2 infection causes a mild disease in most children, SARS-CoV-2 infection may be lethal in a few of them. In the defense against SARS-CoV-2, type I interferons are key players, and several studies have identified a defective or neutralized interferon response as the cause of overwhelming viral infection. However, inappropriate, untimely, or excessive interferon production may also be detrimental to the host. Here, we describe two patients with STAT1 gain-of-function (GOF), a known type I interferonopathy, who died of COVID-19. Whole-exome sequencing and interferon-gamma-activated sequence (GAS) and interferon-sensitive responsive element (ISRE) reporter assay were performed to identify and characterize STAT1 variants. Patient 1 developed hemophagocytic lymphohistiocytosis (HLH) in the context of COVID-19 infection and died in less than a week at the age of 4 years. Patient 2 developed a high fever, cough, and hypoxemia and succumbed to COVID-19 pneumonia at the age of 5 years. Two heterozygous missense variants, p.E563Q and p.K344E, in STAT1 were identified. Functional validation by reporter assay and immunoblot confirmed that both variants are gain-of-function (GOF). GOF variants transiently expressing cells exhibited enhanced upregulation of downstream genes, including ISG15 , MX1 , and OAS1 , in response to IFN-α stimulation. A catastrophic course with HLH or acute respiratory failure is thought to be associated with inappropriate immunoregulatory mechanisms to handle SARS-CoV-2 in STAT1 GOF. While most patients with inborn errors of immunity who developed COVID-19 seem to handle it well, these cases suggest that patients with STAT1-GOF might be at risk of developing fatal complications due to SARS-CoV-2.