Infection rate and virus-induced cytokine secretion in experimental rhinovirus infection in mucosal organ culture: comparison between specimens from patients with chronic rhinosinusitis with nasal polyps and those from normal subjects

Arch Otolaryngol Head Neck Surg. 2008 Apr;134(4):424-7. doi: 10.1001/archotol.134.4.424.

Abstract

Objective: To investigate the difference in susceptibility to rhinovirus (RV) infection and RV-induced inflammatory response between the nasal mucosae from patients with chronic rhinosinusitis with nasal polyps (CRS/NP) and subjects without CRS/NP (hereinafter, normal subjects).

Design: In vitro study.

Setting: Tertiary care rhinology clinic.

Patients: We conducted RV infection experiments on the organ cultures of NPs and inferior turbinate mucosae from 16 patients with CRS/NP and sphenoid sinus and inferior turbinate mucosae from 19 patients who underwent transsphenoidal pituitary surgery.

Main outcome measures: Successful RV-16 infection was determined by positive identification of RV on the surface fluid of organ culture using seminested reverse transcriptase-polymerase chain reaction. Effects of RV on interleukin 6 (IL-6) and IL-8 secretion were measured by enzyme-linked immunosorbent assay.

Results: The successful RV infection was achievable in 9 of 16 NP samples (56.3%) and 9 of 16 turbinate samples (56.3%) from patients with CRS/NP compared with 11 of 19 sphenoid sinus samples (57.9%) and 15 of 19 turbinate samples (78.9%) from normal subjects. The RV infection increased IL-6 and IL-8 secretion 236% and 173%, respectively, in NP samples, and 218% and 178%, respectively, in turbinate samples from patients with CRS/NP; compared with 231% and 145%, respectively, in sphenoid mucosa samples, and 181% and 148%, respectively, in turbinate samples from normal subjects. However, there were no statistical differences among the 4 groups.

Conclusion: These in vitro findings suggest that subjects with CRS/NP mucosa might not be more susceptible to RV infection, and did not secrete more cytokines in response to rhinovirus infection, than those with normal mucosa.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Case-Control Studies
  • Child
  • Chronic Disease
  • Cytokines / metabolism*
  • Disease Susceptibility
  • Female
  • Humans
  • Male
  • Middle Aged
  • Nasal Polyps / complications*
  • Nasal Polyps / metabolism
  • Nasal Polyps / virology
  • Picornaviridae Infections / etiology
  • Picornaviridae Infections / metabolism*
  • Rhinitis / complications*
  • Rhinitis / metabolism
  • Rhinitis / virology
  • Rhinovirus*
  • Sinusitis / complications*
  • Sinusitis / metabolism
  • Sinusitis / virology
  • Tissue Culture Techniques
  • Turbinates / metabolism

Substances

  • Cytokines