Author:
Nakayama Emi E.,Kubota-Koketsu Ritsuko,Sasaki Tadahiro,Suzuki Keita,Uno Kazuko,Shimizu Jun,Okamoto Toru,Matsumoto Hisatake,Matsuura Hiroshi,Hashimoto Shoji,Tanaka Toshio,Harada Hiromasa,Tomita Masafumi,Kaneko Mitsunori,Yoshizaki Kazuyuki,Shioda Tatsuo
Abstract
AbstractA cytokine storm induces acute respiratory distress syndrome, the main cause of death in coronavirus disease 2019 (COVID-19) patients. However, the detailed mechanisms of cytokine induction due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remain unclear. To examine the cytokine production in COVID-19, we mimicked the disease in SARS-CoV-2-infected alveoli by adding the lysate of SARS-CoV-2-infected cells to cultured macrophages or induced pluripotent stem cell-derived myeloid cells. The cells secreted interleukin (IL)-6 after the addition of SARS-CoV-2-infected cell lysate. Screening of 25 SARS-CoV-2 protein-expressing plasmids revealed that the N protein-coding plasmid alone induced IL-6 production. The addition of anti-N antibody further enhanced IL-6 production, but the F(ab’)2 fragment did not. Sera from COVID-19 patients also enhanced IL-6 production, and sera from patients with severer disease induced higher levels of IL-6. These results suggest that anti-N antibody promotes IL-6 production in SARS-CoV-2-infected alveoli, leading to the cytokine storm of COVID-19.
Funder
Japan Agency for Medical Research and Development
Publisher
Springer Science and Business Media LLC
Cited by
16 articles.
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