Early mucosal IFN-α, IP-10, and IL-1RA and synchronized mucosal and systemic immune responses mediate COVID-19 disease progression

This research is crucial for understanding the intricate interplay between mucosal immunity and SARS-CoV-2 infection. By examining the distinct systemic and mucosal immune responses during COVID-19, this study addresses the critical gap in our knowledge of how the body defends itself at the primary site of infection: the respiratory mucosa. The findings shed light on the specific characteristics of the mucosal immune response, including the roles of different antibody isotypes, immune cells, and local factors in controlling viral entry and replication. Furthermore, because this study focuses on <i>de novo</i> immune responses, the results may have broad implications for understanding immune responses to future novel pathogens. Ultimately, this research will contribute to the development of more effective diagnostic tools, therapeutic strategies, and mucosal vaccines to prevent and control COVID-19. By focusing on the often-overlooked mucosal compartment, this work offers a new perspective on comprehending SARS-CoV-2 infection, its implications for public health, and preparedness for future pandemic threats.

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Publication Details

Journal
mBio
Published
2025-11-28
DOI
https://doi.org/10.1128/mbio.01491-25
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
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article

Early mucosal IFN-α, IP-10, and IL-1RA and synchronized mucosal and systemic immune responses mediate COVID-19 disease progression

Mona Agrawal, Nicholas D. Hysmith, Richard J. Webby, Armando S. Flores-Torres et al.
mBio
SARS-CoV-2 and COVID-19 Research
article

Early mucosal IFN-α, IP-10, and IL-1RA and synchronized mucosal and systemic immune responses mediate COVID-19 disease progression

Mona Agrawal, Nicholas D. Hysmith, Richard J. Webby, Armando S. Flores-Torres, Heather S. Smallwood, Michael A. Whitt, Thomas Fabrizio, Laura V. Boywid, Chloe Hundman, Amanda Green, Rachael Keating, Sarah Y. Lang, Paul G. Thomas, A. Blair, John S. Franks, Kristin E. McNair
article en

Abstract

This research is crucial for understanding the intricate interplay between mucosal immunity and SARS-CoV-2 infection. By examining the distinct systemic and mucosal immune responses during COVID-19, this study addresses the critical gap in our knowledge of how the body defends itself at the primary site of infection: the respiratory mucosa. The findings shed light on the specific characteristics of the mucosal immune response, including the roles of different antibody isotypes, immune cells, and local factors in controlling viral entry and replication. Furthermore, because this study focuses on <i>de novo</i> immune responses, the results may have broad implications for understanding immune responses to future novel pathogens. Ultimately, this research will contribute to the development of more effective diagnostic tools, therapeutic strategies, and mucosal vaccines to prevent and control COVID-19. By focusing on the often-overlooked mucosal compartment, this work offers a new perspective on comprehending SARS-CoV-2 infection, its implications for public health, and preparedness for future pandemic threats.

mBioVol. 17(1)
St. Jude Children's Research Hospital (US), University of Tennessee Health Science Center (US), Children’s Foundation (GB), Le Bonheur Children's Hospital (US), Monash University (AU)
Openalex Percentile: Top 56%
SARS-CoV-2 and COVID-19 Research
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