Ventilatory capacity in CLAD is driven by dysfunctional airway structureResearch in context
Pieterjan Kerckhof,
Gene P.L. Ambrocio,
Hanne Beeckmans,
Janne Kaes,
Vincent Geudens,
Saskia Bos,
Lynn Willems,
Astrid Vermaut,
Marie Vermant,
Tinne Goos,
Charlotte De Fays,
Lucia Aversa,
Yousry Mohamady,
Arno Vanstapel,
Michaela Orlitová,
Jan Van Slambrouck,
Xin Jin,
Vimi Varghese,
Iván Josipovic,
Matthieu N. Boone,
Lieven J. Dupont,
Birgit Weynand,
Adriana Dubbeldam,
Dirk E. Van Raemdonck,
Laurens J. Ceulemans,
Ghislaine Gayan-Ramirez,
Laurens J. De Sadeleer,
John E. McDonough,
Bart M. Vanaudenaerde,
Robin Vos
Affiliations
Pieterjan Kerckhof
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Gene P.L. Ambrocio
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium; Division of Pulmonary Medicine, Department of Internal Medicine, University of the Philippines – Philippine General Hospital, Manilla, The Philippines
Hanne Beeckmans
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Janne Kaes
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Vincent Geudens
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Saskia Bos
Newcastle University, Translational and Clinical Research Institute, Newcastle upon Tyne, United Kingdom
Lynn Willems
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Astrid Vermaut
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Marie Vermant
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Tinne Goos
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Charlotte De Fays
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium; Pole of Pneumology, ENT, and Dermatology, Institute of Experimental and Clinical Research, Université Catholique de Louvain, Brussels, Belgium
Lucia Aversa
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Yousry Mohamady
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Arno Vanstapel
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium; Department of Pathology, University Hospitals Leuven, Leuven, Belgium
Michaela Orlitová
Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium
Jan Van Slambrouck
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Xin Jin
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Vimi Varghese
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium; Department of Heart and Lung Transplant, Yashoda Hospitals, Hyderabad, India
Iván Josipovic
Department of Physics and Astronomy, UGCT, Radiation Physics, Ghent University, Gent, Belgium
Matthieu N. Boone
Department of Physics and Astronomy, UGCT, Radiation Physics, Ghent University, Gent, Belgium
Lieven J. Dupont
Department of Respiratory Diseases, University Hospitals Leuven, Leuven, Belgium
Birgit Weynand
Department of Pathology, University Hospitals Leuven, Leuven, Belgium
Adriana Dubbeldam
Department of Radiology, University Hospitals Leuven, Leuven, Belgium
Dirk E. Van Raemdonck
Department of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium
Laurens J. Ceulemans
Department of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium
Ghislaine Gayan-Ramirez
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Laurens J. De Sadeleer
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium; Cell Circuits in Systems Medicine of Lung Disease (Schiller Lab), Institute of Lung Health and Immunity (LHI) / Comprehensive Pneumology Centre (CPC), German Centre for Lung Research, Helmholtz Zentrum München, München, Germany
John E. McDonough
Department of Medicine, McMaster University, Firestone Institute of Respiratory Health, Hamilton, Canada
Bart M. Vanaudenaerde
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of CHROMETA, KU Leuven, Leuven, Belgium
Robin Vos
Department of Respiratory Diseases, University Hospitals Leuven, Leuven, Belgium; Corresponding author. Department of Chronic Diseases, Metabolism and ageing (CHROMETA), Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), KU Leuven and University Hospitals Leuven, Herestraat 49, B-3000, Leuven, Belgium.
Summary: Background: Chronic lung allograft dysfunction (CLAD) encompasses three main phenotypes: bronchiolitis obliterans syndrome (BOS), restrictive allograft syndrome (RAS) and a Mixed phenotype combining both pathologies. How the airway structure in its entirety is affected in these phenotypes is still poorly understood. Methods: A detailed analysis of airway morphometry was applied to gain insights on the effects of airway remodelling on the distribution of alveolar ventilation in end-stage CLAD. Ex vivo whole lung μCT and tissue-core μCT scanning of six control, six BOS, three RAS and three Mixed explant lung grafts (9 male, 9 female, 2014–2021, Leuven, Belgium) were used for digital airway reconstruction and calculation of airway dimensions in relation to luminal obstructions. Findings: BOS and Mixed explants demonstrated airway obstructions of proximal bronchioles (starting at generation five), while RAS explants particularly had airway obstructions in the most distal bronchioles (generation >12). In BOS and Mixed explants 76% and 84% of bronchioles were obstructed, respectively, while this was 22% in RAS. Bronchiolar obstructions were mainly caused by lymphocytic inflammation of the airway wall or fibrotic remodelling, i.e. constrictive bronchiolitis. Proximal bronchiolectasis and imbalance in distal lung ventilation were present in all CLAD phenotypes and explain poor lung function and deterioration of specific lung function parameters. Interpretation: Alterations in the structure of conducting bronchioles revealed CLAD to affect alveolar ventilatory distribution in a regional fashion. The significance of various obstructions, particularly those associated with mucus, is highlighted. Funding: This research was funded with the National research fund Flanders (G060322N), received by R.V.