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Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19

Authors
Daniel Blanco-Melo,Benjamin E. Nilsson-Payant
Wen-Chun Liu,Skyler Uhl,Daisy Hoagland,Rasmus Møller,Tristan X. Jordan,Kohei Oishi,Maryline Panis,David Sachs,Taia T. Wang,Robert E. Schwartz,Jean K. Lim,Randy A. Albrecht,Benjamin R. tenOever,Benjamin Nilsson-Payant,Wen‐Chun Liu,Tristan Jordan,Taia Wang,Robert Schwartz,Jean Lim,Randy Albrecht
+20 authors
,Benjamin tenOever
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Published
May 1, 2020
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Abstract

Viral pandemics, such as the one caused by SARS-CoV-2, pose an imminent threat to humanity. Because of its recent emergence, there is a paucity of information regarding viral behavior and host response following SARS-CoV-2 infection. Here we offer an in-depth analysis of the transcriptional response to SARS-CoV-2 compared with other respiratory viruses. Cell and animal models of SARS-CoV-2 infection, in addition to transcriptional and serum profiling of COVID-19 patients, consistently revealed a unique and inappropriate inflammatory response. This response is defined by low levels of type I and III interferons juxtaposed to elevated chemokines and high expression of IL-6. We propose that reduced innate antiviral defenses coupled with exuberant inflammatory cytokine production are the defining and driving features of COVID-19.

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