The interferon landscape along the respiratory tract impacts the severity of COVID-19

Benedetta Sposito(Boston Children's Hospital), Achille Broggi(Boston Children's Hospital), Laura Pandolfi(Istituti di Ricovero e Cura a Carattere Scientifico), Stefania Crotta(The Francis Crick Institute), Nicola Clementi(Vita-Salute San Raffaele University), Roberto Ferrarese(Vita-Salute San Raffaele University), Sofia Sisti(Vita-Salute San Raffaele University), Elena Criscuolo(Vita-Salute San Raffaele University), Roberto Spreafico(QB3), Jaclyn M. Long(Boston Children's Hospital), Alessandro Ambrosi(Vita-Salute San Raffaele University), Enju Liu(Boston Children's Hospital), Vanessa Frangipane(Istituti di Ricovero e Cura a Carattere Scientifico), Laura Saracino(Istituti di Ricovero e Cura a Carattere Scientifico), Sara Bozzinì(Istituti di Ricovero e Cura a Carattere Scientifico), Laura Marongiu(University of Milano-Bicocca), Fabio A. Facchini(University of Milano-Bicocca), Andrea Bottazzi(Policlinico San Matteo Fondazione), Tommaso Fossali(University of Milan), Riccardo Colombo(University of Milan), Massimo Clementi(Vita-Salute San Raffaele University), Elena Tagliabue(MultiMedica), Janet Chou(Boston Children's Hospital), Antonio E. Pontiroli(University of Milan), Federica Meloni(University of Pavia), Andreas Wack(The Francis Crick Institute), Nicasio Mancini(Vita-Salute San Raffaele University), Ivan Zanoni(Boston Children's Hospital)
Cell
August 19, 2021
Cited by 279Open Access
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Abstract

Severe coronavirus disease 2019 (COVID-19) is characterized by overproduction of immune mediators, but the role of interferons (IFNs) of the type I (IFN-I) or type III (IFN-III) families remains debated. We scrutinized the production of IFNs along the respiratory tract of COVID-19 patients and found that high levels of IFN-III, and to a lesser extent IFN-I, characterize the upper airways of patients with high viral burden but reduced disease risk or severity. Production of specific IFN-III, but not IFN-I, members denotes patients with a mild pathology and efficiently drives the transcription of genes that protect against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In contrast, compared to subjects with other infectious or noninfectious lung pathologies, IFNs are overrepresented in the lower airways of patients with severe COVID-19 that exhibit gene pathways associated with increased apoptosis and decreased proliferation. Our data demonstrate a dynamic production of IFNs in SARS-CoV-2-infected patients and show IFNs play opposing roles at distinct anatomical sites.


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