4.6 Article

Toll-Like Receptor (TLR2 and TLR4) Polymorphisms and Chronic Obstructive Pulmonary Disease

Journal

PLOS ONE
Volume 7, Issue 8, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0043124

Keywords

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Funding

  1. Graduate School for Drug Exploration (GUIDE), University Medical Center Groningen, University of Groningen, the Netherlands
  2. Netherlands Organization for Scientific Research (NWO) [940-35-033]
  3. Netherlands Asthma Foundation (NAF) [37.97.74, 3.2.02.51]
  4. GlaxoSmithKline (NL)
  5. Leiden University Medical Center (LUMC)
  6. University of Groningen (RUG)
  7. AstraZeneca
  8. GSK
  9. Nycomed
  10. Chiesi
  11. Amgen
  12. Boehringer Ingelheim
  13. Centocor
  14. Galapagos
  15. GlaxoSmithKline
  16. Glaxo-SmithKline
  17. Netherlands Asthma Funds

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Toll-like receptors (TLRs) participate in the defence against bacterial infections that are common in patients with Chronic Obstructive Pulmonary Disease (COPD). We studied all tagging SNPs in TLR2 and TLR4 and their associations with the level and change over time of both FEV1 and sputum inflammatory cells in moderate-to-severe COPD. Nine TLR2 SNPs and 17 TLR4 SNPs were genotyped in 110 COPD patients. Associations of SNPs with lung function and inflammatory cells in induced sputum were analyzed cross-sectionally with linear regression and longitudinally with linear mixed-effect models. Two SNPs in TLR2 (rs1898830 and rs11938228) were associated with a lower level of FEV1 and accelerated decline of FEV1 and higher numbers of sputum inflammatory cells. None of the TLR4 SNPs was associated with FEV1 level. Eleven out of 17 SNPs were associated with FEV1 decline, including rs12377632 and rs10759931, which were additionally associated with higher numbers of sputum inflammatory cells at baseline and with increase over time. This is the first longitudinal study showing that tagging SNPs in TLR2 and TLR4 are associated with the level and decline of lung function as well as with inflammatory cell numbers in induced sputum in COPD patients, suggesting a role in the severity and progression of COPD.

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