4.7 Article

Upper respiratory tract bacterial-immune interactions during respiratory syncytial virus infection in infancy

期刊

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 149, 期 3, 页码 966-976

出版社

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2021.08.022

关键词

Airway; bronchiolitis; chemokines; cytokines; growth factors; immune response; infancy; mediation; microbiome; nasopharynx; respiratory syncytial virus; severity; wheezing

资金

  1. National Institute of Allergy and Infectious Diseases [U19AI095227, K24AI77930, HHSN272200900007C, R21AI142321, U19AI110819, R21AI154016, R21AI149262, UG3OD023282]
  2. National Heart, Lung, and Blood Institute [K23HL148638, R01HL146401]
  3. National Institute of General Medical Sciences [R01GM140464]
  4. Parker B. Francis Fellowship Program
  5. Vanderbilt Institute for Clinical and Translational Research (National Center for Advancing Translational Sciences) [UL1TR000445]
  6. Department of Pediatrics at Vanderbilt University Medical Center (Eunice Kennedy Shriver National Institute of Child Health and Human Development) [K12HD087023]
  7. Vanderbilt Building Interdisciplinary Research Careers in Women's Health K-12 program (Eunice Kennedy Shriver National Institute of Child Health and Human Development) [K12HD04348318]
  8. Vanderbilt Technologies for Advanced Genomics Core (National Institutes of Health) [UL1RR024975, P30CA68485, P30EY08126, G20RR030956]

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The study found that the upper respiratory tract (URT) microbiome during RSV ARI in infancy is associated with the acute local immune response, disease severity, and number of wheezing episodes in the fourth year of life. The diversity of the URT microbiome is related to the course of RSV ARI, and there are complex interactions between the URT microbiome and the immune system.
Background: The risk factors determining short-and long-term morbidity following acute respiratory infection (ARI) due to respiratory syncytial virus (RSV) in infancy remain poorly understood. Objectives: Our aim was to examine the associations of the upper respiratory tract (URT) microbiome during RSV ARI in infancy with the acute local immune response and short-and long-term clinical outcomes. Methods: We characterized the URT microbiome by 16S ribosomal RNA sequencing and assessed the acute local immune response by measuring 53 immune mediators with high throughput immunoassays in 357 RSV-infected infants. Our short-and long-term clinical outcomes included several markers of disease severity and the number of wheezing episodes in the fourth year of life, respectively. Results: We found several specific URT bacterial-immune mediator associations. In addition, the Shannon alpha-diversity index of the URT microbiome was associated with a higher respiratory severity score (beta = .50 [95% CI = 0.13-0.86]), greater odds of a lower ARI (odds ratio = 1.63 [95% CI = 1.10-2.43]), and higher number of wheezing episodes in the fourth year of life (beta = 0.89 [95% CI = 0.37-1.40]). The Jaccard beta-diversity index of the URT microbiome differed by level of care required (P = .04). Furthermore, we found an interaction between the Shannon alpha-diversity index of the URT microbiome and the first principal component of the acute local immune response on the respiratory severity score (P = .048). Conclusions: The URT microbiome during RSV ARI in infancy is associated with the acute local immune response, disease severity, and number of wheezing episodes in the fourth year of life. Our results also suggest complex URT bacterial-immune interactions that can affect the severity of the RSV ARI.

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