Affiliations 

  • 1 Dept of Respiratory and Critical Care Medicine, Singapore General Hospital, Singapore
  • 2 Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore
  • 3 Dept of Biological Sciences, National University of Singapore, Singapore
  • 4 Dept of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong
  • 5 Dept of Medicine, University of Malaya, Kuala Lumpur, Malaysia
  • 6 Dept of Respiratory and Critical Care Medicine, Tan Tock Seng Hospital, Singapore
  • 7 Dept of Respiratory and Critical Care Medicine, Changi General Hospital, Singapore
  • 8 Living Systems Institute and Department of Mathematics, College of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter, UK
  • 9 Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore schotirmall@ntu.edu.sg
Eur Respir J, 2023 Jan;61(1).
PMID: 35926878 DOI: 10.1183/13993003.00507-2022

Abstract

BACKGROUND: Variable clinical outcomes are reported with fungal sensitisation in chronic obstructive pulmonary disease (COPD), and it remains unclear which fungi and what allergens associate with the poorest outcomes. The use of recombinant as opposed to crude allergens for such assessment is unknown.

METHODS: A prospective multicentre assessment of stable COPD (n=614) was undertaken in five hospitals across three countries: Singapore, Malaysia and Hong Kong. Clinical and serological assessment was performed against a panel of 35 fungal allergens including crude and recombinant Aspergillus and non-Aspergillus allergens. Unsupervised clustering and topological data analysis (TDA) approaches were employed using the measured sensitisation responses to elucidate if sensitisation subgroups exist and their related clinical outcomes.

RESULTS: Aspergillus fumigatus sensitisation was associated with increased exacerbations in COPD. Unsupervised cluster analyses revealed two "fungal sensitisation" groups. The first was characterised by Aspergillus sensitisation and increased exacerbations, poorer lung function and worse prognosis. Polysensitisation in this group conferred even poorer outcome. The second group, characterised by Cladosporium sensitisation, was more symptomatic. Significant numbers of individuals demonstrated sensitisation responses to only recombinant (as opposed to crude) A. fumigatus allergens f 1, 3, 5 and 6, and exhibited increased exacerbations, poorer lung function and an overall worse prognosis. TDA validated these findings and additionally identified a subgroup within Aspergillus-sensitised COPD of patients with frequent exacerbations.

CONCLUSION: Aspergillus sensitisation is a treatable trait in COPD. Measuring sensitisation responses to recombinant Aspergillus allergens identifies an important patient subgroup with poor COPD outcomes that remains overlooked by assessment of only crude Aspergillus allergens.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.