IFN Lambda 3/4 locus polymorphisms and IFN Lambda 3 circulating levels are associated with COPD severity and outcomes

  • Adrian Egli
  • , Jyotshna Mandal
  • , Desiree M. Schumann*
  • , Michael Roth
  • , Brad Thomas
  • , D. Lorne Tyrrell
  • , Francesco Blasi
  • , Kostantinos Kostikas
  • , Wim Boersma
  • , Branislava Milenkovic
  • , Alicia Lacoma
  • , Katharina Rentsch
  • , Gernot G. U. Rohde
  • , Renaud Louis
  • , Joachim G. Aerts
  • , Tobias Welte
  • , Antoni Torres
  • , Michael Tamm
  • , Daiana Stolz
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background: Interferon lambdas (IFNLs) have important anti-viral/bacterial and immunomodulatory functions in the respiratory tract. How do IFNLs impact COPD and its exacerbations? Methods: Five hundred twenty eight patients were recruited in a prospective observational multicentre cohort (PROMISE) study. The genetic polymorphisms (rs8099917 and rs12979860) within the IFNL3/4 gene region and circulating levels of IFNL3 in COPD patients were determined and associated with disease activity and outcome during a median follow-up of 24 months. Results: The GG genotype significantly influenced severe exacerbation rate (42 vs. 23%; p = 0.032) and time to severe exacerbation (HR = 2.260; p = 0.012). Compared to the TT or TG genotypes, the GG genotype was associated with severe dyspnoea (modified medical research council score >= median 3; 22 vs 42%, p = 0.030). The CC genotype of the rs12979860 SNP was associated with a poorer prognosis (body mass index, airflow obstruction, dyspnea and exercise capacity index >= median 4; 46 vs. 36% TC vs. 20.5% TT; p = 0.031). Patients with stable COPD and at exacerbation had significantly lower circulating IFNL3 compared to healthy controls (p < 0.001 and p < 0.001, respectively). Circulating IFNL3 correlated to post-bronchodilator FEV1% predicted and the tissue maturation biomarker Pro-collagen 3. Conclusion: IFNL3/4 polymorphisms and circulating IFNL3 may be associated with disease activity and outcomes in COPD.
Original languageEnglish
Article number51
Number of pages9
JournalBMC Pulmonary Medicine
Volume18
Issue number1
DOIs
Publication statusPublished - 21 Mar 2018

Keywords

  • Interleukin 28B
  • Cohort
  • Mortality
  • Biomarker
  • Single nucleotide polymorphisms
  • CHRONIC HEPATITIS-C
  • OBSTRUCTIVE PULMONARY-DISEASE
  • GENOME-WIDE ASSOCIATION
  • GENETIC-VARIATION
  • INTERFERON-LAMBDA
  • IL28B
  • ASTHMA
  • EXACERBATION
  • EXPRESSION
  • BIOMARKERS

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