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      Mucus plugs in patients with asthma linked to eosinophilia and airflow obstruction

      research-article
      1 , 2 , 3 , 4 , 4 , 5 , 1 , 1 , 1 , 5 , 6 , 4 , 7 , 8 , 8 , 9 , 10 , 11 , 11 , 12 , 12 , 1 , 1 , 1 , 1 , The National Heart Lung and Blood Institute (NHLBI) Severe Asthma Research Program (SARP) 13
      The Journal of Clinical Investigation
      American Society for Clinical Investigation
      Pulmonology, Asthma, Cytokines, Th2 response

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          Abstract

          BACKGROUND. The link between mucus plugs and airflow obstruction has not been established in chronic severe asthma, and the role of eosinophils and their products in mucus plug formation is unknown.

          METHODS. In clinical studies, we developed and applied a bronchopulmonary segment–based scoring system to quantify mucus plugs on multidetector computed tomography (MDCT) lung scans from 146 subjects with asthma and 22 controls, and analyzed relationships among mucus plug scores, forced expiratory volume in 1 second (FEV1), and airway eosinophils. Additionally, we used airway mucus gel models to explore whether oxidants generated by eosinophil peroxidase (EPO) oxidize cysteine thiol groups to promote mucus plug formation.

          RESULTS. Mucus plugs occurred in at least 1 of 20 lung segments in 58% of subjects with asthma and in only 4.5% of controls, and the plugs in subjects with asthma persisted in the same segment for years. A high mucus score (plugs in ≥ 4 segments) occurred in 67% of subjects with asthma with FEV1 of less than 60% of predicted volume, 19% with FEV1 of 60%–80%, and 6% with FEV1 greater than 80% ( P < 0.001) and was associated with marked increases in sputum eosinophils and EPO. EPO catalyzed oxidation of thiocyanate and bromide by H 2 O 2 to generate oxidants that crosslink cysteine thiol groups and stiffen thiolated hydrogels.

          CONCLUSION. Mucus plugs are a plausible mechanism of chronic airflow obstruction in severe asthma, and EPO-generated oxidants may mediate mucus plug formation. We propose an approach for quantifying airway mucus plugging using MDCT lung scans and suggest that treating mucus plugs may improve airflow in chronic severe asthma.

          TRIAL REGISTRATION. Clinicaltrials.gov NCT01718197, NCT01606826, NCT01750411, NCT01761058, NCT01761630, NCT01759186, NCT01716494, and NCT01760915.

          FUNDING. NIH grants P01 HL107201, R01 HL080414, U10 HL109146, U10 HL109164, U10 HL109172, U10 HL109086, U10 HL109250, U10 HL109168, U10 HL109257, U10 HL109152, and P01 HL107202 and National Center for Advancing Translational Sciences grants UL1TR0000427, UL1TR000448, and KL2TR000428.

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          Author and article information

          Contributors
          Journal
          J Clin Invest
          J. Clin. Invest
          J Clin Invest
          The Journal of Clinical Investigation
          American Society for Clinical Investigation
          0021-9738
          1558-8238
          5 February 2018
          1 March 2018
          1 June 2018
          : 128
          : 3
          : 997-1009
          Affiliations
          [1 ]Division of Pulmonary and Critical Care Medicine, Department of Medicine and Cardiovascular Research Institute, and
          [2 ]Department of Radiology and Biomedical Imaging, UCSF, San Francisco, California, USA.
          [3 ]Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri, USA.
          [4 ]Department of Medical Physics and Department of Radiology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
          [5 ]Division of Cardiovascular and Pulmonary Imaging, Department of Radiology, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA.
          [6 ]Division of Pulmonary and Critical Care Medicine, Department of Medicine, Washington University, St. Louis, Missouri, USA.
          [7 ]Allergy, Pulmonary and Critical Care Medicine Division, University of Wisconsin School of Medicine, Madison, Wisconsin, USA.
          [8 ]Pulmonary and Critical Care Medicine Division, Brigham and Women’s Hospital, Boston, Massachusetts, USA.
          [9 ]Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
          [10 ]Pulmonary, Allergy and Critical Care Medicine Division, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
          [11 ]Center for Genomics and Personalized Medicine Research, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
          [12 ]Division of Biostatistics and Bioinformatics, Department of Public Health Sciences, Penn State University, Hershey, Pennsylvania, USA.
          [13 ]The NHLBI SARP investigators are detailed in the Supplemental Acknowledgments.
          Author notes
          Address correspondence to: John Fahy, Room 1303, Health Sciences East, UCSF, 513 Parnassus Avenue, San Francisco, California 94143, USA. Phone: 415.476.9940; Email: john.fahy@ 123456ucsf.edu .
          Author information
          http://orcid.org/0000-0001-6328-8994
          Article
          PMC5824874 PMC5824874 5824874 95693
          10.1172/JCI95693
          5824874
          29400693
          fb65d630-5e81-4fdb-a235-e12b01af5ec4
          Copyright © 2018, American Society for Clinical Investigation
          History
          : 21 June 2017
          : 19 December 2017
          Funding
          Funded by: NIH
          Award ID: P01 HL107201
          Funded by: NIH
          Award ID: R01 HL080414
          Funded by: NIH
          Award ID: U10 HL109146
          Funded by: NIH
          Award ID: U10 HL109164
          Funded by: NIH
          Award ID: U10 HL109172
          Funded by: NIH
          Award ID: U10 HL109086
          Funded by: NIH
          Award ID: U10 HL109250
          Funded by: NIH, https://doi.org/10.13039/100007189;
          Award ID: U10 HL109168
          Funded by: NIH
          Award ID: U10 HL109257
          Funded by: NIH
          Award ID: U10 HL109152
          Funded by: NIH
          Award ID: P01 HL107202
          Funded by: NCATS
          Award ID: UL1TR0000427
          Funded by: NCATS
          Award ID: UL1TR000448
          Funded by: NCATS
          Award ID: KL2TR000428
          Categories
          Clinical Medicine

          Pulmonology,Asthma,Cytokines,Th2 response
          Pulmonology, Asthma, Cytokines, Th2 response

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