Sex differences in innate anti-viral immune responses to respiratory viruses and in their clinical outcomes in a birth cohort study
File(s)s41598-021-03044-x.pdf (1.93 MB)
Published version
Author(s)
Type
Journal Article
Abstract
The mechanisms explaining excess morbidity and mortality in respiratory infections among males are poorly understood. Innate immune responses are critical in protection against respiratory virus infections. We hypothesised that innate immune responses to respiratory viruses may be deficient in males. We stimulated peripheral blood mononuclear cells from 345 participants at age 16 years in a population-based birth cohort with three live respiratory viruses (rhinoviruses A16 and A1, and respiratory syncytial virus) and two viral mimics (R848 and CpG-A, to mimic responses to SARS-CoV-2) and investigated sex differences in interferon (IFN) responses. IFN-α responses to all viruses and stimuli were 1.34–2.06-fold lower in males than females (P = 0.018 − < 0.001). IFN-β, IFN-γ and IFN-induced chemokines were also deficient in males across all stimuli/viruses. Healthcare records revealed 12.1% of males and 6.6% of females were hospitalized with respiratory infections in infancy (P = 0.017). In conclusion, impaired innate anti-viral immunity in males likely results in high male morbidity and mortality from respiratory virus infections.
Date Issued
2021-12-09
Date Acceptance
2021-11-23
Citation
Scientific Reports, 2021, 11 (23741), pp.1-15
ISSN
2045-2322
Publisher
Nature Publishing Group
Start Page
1
End Page
15
Journal / Book Title
Scientific Reports
Volume
11
Issue
23741
Copyright Statement
© The Author(s) 2021. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Sponsor
Asthma UK
Asthma UK
National Institute for Health Research
Commission of the European Communities
Identifier
https://www.nature.com/articles/s41598-021-03044-x
Grant Number
CH11SJ
CH11SJ
NF-SI-0514-10092
788575
Subjects
Science & Technology
Multidisciplinary Sciences
Science & Technology - Other Topics
PLASMACYTOID DENDRITIC CELLS
BRONCHIAL EPITHELIAL-CELLS
IFN-ALPHA PRODUCTION
SYNCYTIAL VIRUS
INTERFERON BETA-1B
MEDIATED RESPONSE
ASTHMA
INFECTIONS
RHINOVIRUS
DEFICIENT
Adolescent
Birth Cohort
Cohort Studies
Female
Humans
Imidazoles
Immunity, Innate
Interferons
Leukocytes, Mononuclear
Male
Oligodeoxyribonucleotides
Picornaviridae Infections
Respiratory Syncytial Virus Infections
Respiratory Syncytial Virus, Human
Respiratory Tract Infections
Rhinovirus
SARS-CoV-2
Sex Factors
Leukocytes, Mononuclear
Humans
Respiratory Syncytial Virus, Human
Rhinovirus
Respiratory Tract Infections
Respiratory Syncytial Virus Infections
Picornaviridae Infections
Imidazoles
Interferons
Oligodeoxyribonucleotides
Cohort Studies
Sex Factors
Adolescent
Female
Male
Immunity, Innate
SARS-CoV-2
Birth Cohort
Publication Status
Published
Date Publish Online
2021-12-09