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Sex-Based Differences in Susceptibility to Severe Acute Respiratory Syndrome Coronavirus Infection

Rudragouda Channappanavar, Craig Fett, Matthias Mack, Patrick P. Ten Eyck, David K. Meyerholz and Stanley Perlman
J Immunol April 1, 2017, 1601896; DOI: https://doi.org/10.4049/jimmunol.1601896
Rudragouda Channappanavar
*Department of Microbiology, University of Iowa, Iowa City, IA 52242;
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Craig Fett
*Department of Microbiology, University of Iowa, Iowa City, IA 52242;
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Matthias Mack
†Department of Internal Medicine, University Hospital Regensburg, Regensburg 93042, Germany;
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Patrick P. Ten Eyck
‡Institute for Clinical and Translational Science, University of Iowa, Iowa City, IA 52242; and
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David K. Meyerholz
§Department of Pathology, University of Iowa, Iowa City, IA 52242
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Stanley Perlman
*Department of Microbiology, University of Iowa, Iowa City, IA 52242;
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Abstract

Pathogenic human coronaviruses (CoVs), such as the severe acute respiratory syndrome (SARS)-CoV and the Middle East respiratory syndrome–CoV, cause acute respiratory illness. Epidemiological data from the 2002–2003 SARS epidemic and recent Middle East respiratory syndrome outbreak indicate that there may be sex-dependent differences in disease outcomes. To investigate these differences, we infected male and female mice of different age groups with SARS-CoV and analyzed their susceptibility to the infection. Our results showed that male mice were more susceptible to SARS-CoV infection compared with age-matched females. The degree of sex bias to SARS-CoV infection increased with advancing age, such that middle-aged mice showed much more pronounced differences compared with young mice. Enhanced susceptibility of male mice to SARS-CoV was associated with elevated virus titers, enhanced vascular leakage, and alveolar edema. These changes were accompanied by increased accumulation of inflammatory monocyte macrophages and neutrophils in the lungs of male mice, and depletion of inflammatory monocyte macrophages partially protected these mice from lethal SARS. Moreover, the sex-specific differences were independent of T and B cell responses. Furthermore, ovariectomy or treating female mice with an estrogen receptor antagonist increased mortality, indicating a protective effect for estrogen receptor signaling in mice infected with SARS-CoV. Together, these data suggest that sex differences in the susceptibility to SARS-CoV in mice parallel those observed in patients and also identify estrogen receptor signaling as critical for protection in females.

Footnotes

  • This work was supported in part by the National Institutes of Health (Grants P01 AI060699 and R01 AI091322).

  • The online version of this article contains supplemental material.

  • Received November 7, 2016.
  • Accepted March 10, 2017.
  • Copyright © 2017 by The American Association of Immunologists, Inc.
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The Journal of Immunology: 206 (8)
The Journal of Immunology
Vol. 206, Issue 8
15 Apr 2021
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Sex-Based Differences in Susceptibility to Severe Acute Respiratory Syndrome Coronavirus Infection
Rudragouda Channappanavar, Craig Fett, Matthias Mack, Patrick P. Ten Eyck, David K. Meyerholz, Stanley Perlman
The Journal of Immunology April 1, 2017, 1601896; DOI: 10.4049/jimmunol.1601896

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Sex-Based Differences in Susceptibility to Severe Acute Respiratory Syndrome Coronavirus Infection
Rudragouda Channappanavar, Craig Fett, Matthias Mack, Patrick P. Ten Eyck, David K. Meyerholz, Stanley Perlman
The Journal of Immunology April 1, 2017, 1601896; DOI: 10.4049/jimmunol.1601896
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Print ISSN 0022-1767        Online ISSN 1550-6606