Neutrophilic inflammation promotes SARS-CoV-2 infectivity and augments the inflammatory responses in airway epithelial cells

中性粒细胞炎症促进 SARS-CoV-2 传染性并增强呼吸道上皮细胞的炎症反应

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作者:Ben A Calvert, Erik J Quiroz, Zareeb Lorenzana, Ngan Doan, Seongjae Kim, Christiana N Senger, Jeffrey J Anders, Wiliam D Wallace, Matthew P Salomon, Jill Henley, Amy L Ryan

Conclusions

This study reveals a key role for neutrophil-epithelial interactions in determining inflammation and infectivity.

Methods

To determine the impact of neutrophil-epithelial interactions on the infectivity and inflammatory responses to SARS-CoV-2 infection, we developed a co-culture model of airway neutrophilia. This model was infected with live SARS-CoV-2 virus the epithelial response to infection was evaluated.

Results

SARS-CoV-2 infection of airway epithelium alone does not result in a notable pro-inflammatory response from the epithelium. The addition of neutrophils induces the release of proinflammatory cytokines and stimulates a significantly augmented proinflammatory response subsequent SARS-CoV-2 infection. The resulting inflammatory responses are polarized with differential release from the apical and basolateral side of the epithelium. Additionally, the integrity of the \epithelial barrier is impaired with notable epithelial damage and infection of basal stem cells. Conclusions: This study reveals a key role for neutrophil-epithelial interactions in determining inflammation and infectivity.

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