Fungal allergens induce cathelicidin LL-37 expression in chronic rhinosinusitis patients in a nasal explant model

Am J Rhinol. 2007 May-Jun;21(3):367-72. doi: 10.2500/ajr.2007.21.3025.

Abstract

Background: Fungus is thought to play an important role in some subgroups of chronic rhinosinusitis (CRS) patients with eosinophilic mucus (EMCRS). The cathelicidin LL-37 is an important innate defense peptide with antimicrobial activity but its responses in CRS and EMCRS patients have not been established. We investigated the innate immune responses of LL-37 in nasal tissue from CRS and EMCRS patients to fungal allergen challenge.

Methods: The levels of LL-37 produced by nasal tissue and secreted in response to fungal allergen challenge were determined by a nasal tissue explant in vitro model. LL-37 mRNA and protein levels were quantified by real-time reverse-transcriptase-polymerase chain reaction and immunoassay methods.

Results: LL-37 mRNA expression in CRS, but not EMCRS patients, is significantly upregulated by Aspergillus (mean fourfold increase) and Alternaria (mean sixfold increase) extracts in a dose-response manner (p < 0.001). LL-37 peptide levels in the nasal tissue from CRS patients are increased in response to Alternaria (p < 0.05). In contrast, with EMCRS patients, the expression of LL-37 peptide in nasal tissue is increased with Aspergillus (p < 0.001) but is reduced with Alternaria. We also observed a trend where levels of secreted LL-37 were decreased with higher doses of Alternaria and Aspergillus extracts.

Conclusion: LL-37 is significantly up-regulated at the mRNA and protein level in CRS patients in response to fungal allergens. However, EMCRS patients do not show increased LL-37 at either the mRNA or the protein level in response to Alternaria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens*
  • Alternaria / isolation & purification
  • Antimicrobial Cationic Peptides / genetics*
  • Aspergillus / isolation & purification
  • Biopsy
  • Cathelicidins
  • Cells, Cultured
  • Fungi
  • Humans
  • Lipopolysaccharides
  • Multigene Family*
  • Paranasal Sinuses / pathology
  • Paranasal Sinuses / surgery
  • RNA, Messenger / genetics
  • Rhinitis / genetics
  • Rhinitis / microbiology
  • Rhinitis / pathology
  • Rhinitis / surgery*
  • Sinusitis / genetics
  • Sinusitis / microbiology
  • Sinusitis / pathology
  • Sinusitis / surgery*
  • Up-Regulation

Substances

  • Allergens
  • Antimicrobial Cationic Peptides
  • Lipopolysaccharides
  • RNA, Messenger
  • Cathelicidins