IL-13 Protects against SARS-CoV-2?
Peebles Jr discusses the paper by Bonser et al which examines the effects of IL-13 on SARS-CoV-2 infection of differentiated human bronchial epithelial cells (HBECs) cultured at an air-liquid interface. The authors report that IL-13 decreased viral RNA recovered from SARS-CoV-2-infected HBECs and re...
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Veröffentlicht in: | American journal of respiratory cell and molecular biology 2022-04, Vol.66 (4), p.351-352 |
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Sprache: | eng |
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Zusammenfassung: | Peebles Jr discusses the paper by Bonser et al which examines the effects of IL-13 on SARS-CoV-2 infection of differentiated human bronchial epithelial cells (HBECs) cultured at an air-liquid interface. The authors report that IL-13 decreased viral RNA recovered from SARS-CoV-2-infected HBECs and reduced double-stranded RNA, a marker of viral replication. This IL-13-mediated inhibition of SARS-CoV-2 infection of HBECs was independent of either IL-13-induced mucus gel or SAM pointed domain-containing Ets transcription factor expression (SPDEF) , suggesting that IL-13 had antiviral effects unrelated to its ability to induce a mucus barrier. They also found that mucus inhibited SARS-CoV-2 infection of HBECs in cells not cultured with IL-13 compared with HBECs in which mucus had been removed by washing. The authors further performed bulk RNA sequencing from HBECs from six subjects who were cultured with IL-13 or IFN-α and were subsequently infected with SARS-CoV-2 and, not surprisingly, found that there were nonredundant differential effects of these cytokines on viral-induced gene expression. |
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ISSN: | 1044-1549 1535-4989 |
DOI: | 10.1165/rcmb.2021-0562ED |