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Obesity Correlates With Pronounced Aberrant Innate Immune Responses in Hospitalized Aged COVID-19 Patients

  • Michael Z. Zulu
  • , Suhas Sureshchandra
  • , Amanda N. Pinski
  • , Brianna Doratt
  • , Weining Shen
  • , Ilhem Messaoudi

Producción científica: Articlerevisión exhaustiva

12 Citas (Scopus)

Resumen

Both age and obesity are leading risk factors for severe coronavirus disease 2019 (COVID-19), which is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Specifically, although most infections occur in individuals under the age of 55 years, 95% of hospitalizations, admissions to the intensive care unit, and deaths occur in those over the age of 55 years. Moreover, hospitalized COVID-19 patients have a higher prevalence of obesity. It is generally believed that chronic low-grade inflammation and dysregulated innate and adaptive immune responses that are associated with aging and obesity are responsible for this elevated risk of severe disease. However, the impact of advanced age and obesity on the host response to SARS-CoV-2 infection remains poorly defined. In this study, we assessed changes in the concentration of soluble immune mediators, IgG antibody titers, frequency of circulating immune cells, and cytokine responses to mitogen stimulation as a function of BMI and age. We detected significant negative correlations between BMI and myeloid immune cell subsets that were more pronounced in aged patients. Similarly, inflammatory cytokine production by monocytes was also negatively correlated with BMI in aged patients. These data suggest that the BMI-dependent impact on host response to SARS-CoV-2 is more pronounced on innate responses of aged patients.

Idioma originalEnglish
Número de artículo760288
PublicaciónFrontiers in Immunology
Volumen12
DOI
EstadoPublished - oct 11 2021

Nota bibliográfica

Publisher Copyright:
© Copyright © 2021 Zulu, Sureshchandra, Pinski, Doratt, Shen and Messaoudi.

Financiación

This study was supported by the National Cancer Research Resources and the National Center for Advancing We would like to thank Hannah Debray and Danielle Gerken for their assistance with sample processing and experiments. The authors wish to acknowledge the support of the Chao Family Comprehensive Tissue Shared Resource, supported by the National Cancer Institutes of Health under the award number P30CA062203.

FinanciadoresNúmero del financiador
National Institutes of Health/National Cancer InstituteP30CA062203
National Cancer Research Resources
National Center for Research Resources and National Center for Advancing Translational Sciences
National Center for Advancing Translational Sciences (NCATS)UL1TR001414

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Immunology and Allergy
    • Immunology

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