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      Elevated Levels of Type 2 Respiratory Innate Lymphoid Cells in Human Infants with Severe Respiratory Syncytial Virus Bronchiolitis

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          Abstract

          Rationale: Studies of the immune responses at the site of respiratory syncytial virus (RSV) infection are sparse despite nearly five decades of research into understanding RSV disease.

          Objectives: To investigate the role of mucosal innate immune responses to RSV and respiratory viral load in infants hospitalized with the natural disease.

          Methods: Cytokines, viral load, and type 2 innate lymphoid cell (ILC2) levels in nasal aspirates, collected within 24 hours of enrollment, from infants hospitalized with RSV infection were quantified.

          Measurements and Main Results: RSV severity in infants was categorized based on admission to the general ward (moderate) or the pediatric ICU (severe). Evaluable subjects included 30 patients with severe and 63 patients with moderate disease (median age, 74 d; range, 9–297 d). ILC2s were found in the nasal aspirates of patients with severe disease (0.051% of total respiratory CD45 + cells) to a significantly greater extent than in patients with moderate disease (0.018%, P = 0.004). Levels of IL-4, IL-13, IL-33, and IL-1β were significantly higher in nasal aspirates of patients with severe disease compared with those of patients with moderate disease. Factors associated with disease severity were gestational age (odds ratio, 0.49; 95% confidence interval, 0.29–0.82; P = 0.007) and IL-4 (odds ratio, 9.67; 95% confidence interval, 2.45–38.15; P = 0.001).

          Conclusions: This study shows, for the first time, that elevated levels of ILC2s is associated with infant RSV severity. The findings highlight the dominance of type-2 responses to RSV infection in infants and suggest an important role of ILC2 in shaping the immune response early during RSV infection.

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          Author and article information

          Journal
          Am J Respir Crit Care Med
          Am J Respir Crit Care Med
          ajrccm
          American Journal of Respiratory and Critical Care Medicine
          American Thoracic Society
          1073-449X
          1535-4970
          1 December 2019
          1 December 2019
          1 December 2019
          : 200
          : 11
          : 1414-1423
          Affiliations
          [ 1 ]Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana
          [ 2 ]Department of Comparative Biomedical Sciences, Louisiana State University School of Veterinary Medicine, Baton Rouge, Louisiana
          [ 3 ]Department of Pediatrics
          [ 4 ]Department of Preventive Medicine, and
          [ 6 ]Department of Microbiology, Immunology, and Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee; and
          [ 5 ]Children’s Foundation Research Institute, Le Bonheur Children’s Hospital, Memphis, Tennessee
          Author notes
          Correspondence and requests for reprints should be addressed to Stephania A. Cormier, Ph.D., Department of Biological Sciences, Louisiana State University, 202 Life Sciences Building, Baton Rouge, LA 70803. E-mail: stephaniacormier@ 123456lsu.edu .
          Author information
          http://orcid.org/0000-0002-6050-6172
          Article
          PMC6884055 PMC6884055 6884055 201812-2366OC
          10.1164/rccm.201812-2366OC
          6884055
          31237777
          2789855c-606a-4aa8-8d7a-1703e045c5fa
          Copyright © 2019 by the American Thoracic Society
          History
          : 20 December 2018
          : 25 June 2019
          Page count
          Figures: 4, Tables: 1, Pages: 10
          Categories
          Original Articles
          Pediatrics and Lung Development/Pulmonary Infections

          immune response,severity,respiratory syncytial virus,infant,type 2 innate lymphoid cell

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