Phenotypical diversity of airway morphology in chronic lung graft vs. host disease after stem cell transplantation.


Journal

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
ISSN: 1530-0285
Titre abrégé: Mod Pathol
Pays: United States
ID NLM: 8806605

Informations de publication

Date de publication:
06 2019
Historique:
received: 08 10 2018
accepted: 11 12 2018
revised: 10 12 2018
pubmed: 7 2 2019
medline: 21 4 2020
entrez: 7 2 2019
Statut: ppublish

Résumé

Pulmonary graft vs. host disease is a diverse and underestimated complication following allogenic hematopoietic stem cell transplantation. We aimed to compare the airway architecture with chronic lung allograft dysfunction post lung transplantation. Inflated explant lungs from graft vs. host disease patients were compared with lungs with chronic lung allograft dysfunction following lung transplantation, and control lungs using a combination of CT, microCT, and histology (n = 6 per group) and pathology in the (small) airways was further quantified and analyzed. Following allogenic hematopoietic stem cell transplantation, three patients presented as bronchiolitis obliterans syndrome and three patients showed interstitial changes and restriction. The CT analysis demonstrated a strong similarity between bronchiolitis obliterans syndrome after lung transplantation and post allogenic hematopoietic stem cell transplantation, evidenced by severe ( > 50%) airway obstruction from generation 9, with 70.8% of the airways ending in obstruction. Further analysis indicated that the airways either collapsed or accumulated matrix along a segment of the airway. In patients with restriction and interstitial changes following allogenic hematopoietic stem cell transplantation, the degree of airway obstruction was lower compared with bronchiolitis obliterans syndrome post allogenic hematopoietic stem cell transplantation, but similar to restrictive allograft syndrome post lung transplantation, showing a lower proportion of airway obstruction (20-35%), decreased number of terminal bronchioles per lung (p < 0.01), and parenchymal fibrosis. We observed similarities in the airway and parenchymal morphometric changes in lung graft vs. host disease and with chronic lung allograft dysfunction following lung transplantation, suggesting similar pathophysiological mechanisms.

Identifiants

pubmed: 30723292
doi: 10.1038/s41379-019-0203-2
pii: S0893-3952(22)01063-8
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

817-829

Auteurs

Stijn E Verleden (SE)

Lung Transplant Unit, Department of Chronic diseases, Metabolism and Aging, KU Leuven, Leuven, Belgium. stijn.verleden@med.kuleuven.be.

John E McDonough (JE)

Lung Transplant Unit, Department of Chronic diseases, Metabolism and Aging, KU Leuven, Leuven, Belgium.

Helene Schoemans (H)

Department of Hematology, University Hospital Leuven and KU Leuven, Leuven, Belgium.

Christiane Knoop (C)

Unite de Transplantation Cardiaque et Pulmonaire, Université Libre de Bruxelles, Brussels, Belgium.

Johny Verschakelen (J)

Department of Imaging and Pathology, KU Leuven, Leuven, Belgium.

Adriana Dubbeldam (A)

Department of Imaging and Pathology, KU Leuven, Leuven, Belgium.

Matthieu N Boone (MN)

Department of Physics and Astronomy, Radiation Physics-Centre for X-ray Tomography, Ghent University, Ghent, Belgium.

Luc Van Hoorebeke (L)

Department of Physics and Astronomy, Radiation Physics-Centre for X-ray Tomography, Ghent University, Ghent, Belgium.

Erik Verbeken (E)

Department of Imaging and Pathology, KU Leuven, Leuven, Belgium.

Birgit Weynand (B)

Department of Imaging and Pathology, KU Leuven, Leuven, Belgium.

Dirk Van Raemdonck (D)

Lung Transplant Unit, Department of Chronic diseases, Metabolism and Aging, KU Leuven, Leuven, Belgium.

Geert M Verleden (GM)

Lung Transplant Unit, Department of Chronic diseases, Metabolism and Aging, KU Leuven, Leuven, Belgium.

Robin Vos (R)

Lung Transplant Unit, Department of Chronic diseases, Metabolism and Aging, KU Leuven, Leuven, Belgium.

Bart M Vanaudenaerde (BM)

Lung Transplant Unit, Department of Chronic diseases, Metabolism and Aging, KU Leuven, Leuven, Belgium.

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