T280M variation of the CX3C receptor gene is associated with increased risk for severe respiratory syncytial virus bronchiolitis

Pediatr Infect Dis J. 2006 May;25(5):410-4. doi: 10.1097/01.inf.0000214998.16248.b7.

Abstract

Background: Recent data suggest that immunologic response during respiratory syncytial virus (RSV) infection is partially modified through interaction of viral G glycoprotein with the host's chemokine receptor, CX3CR1. We hypothesized that two nonsynonymous, single-nucleotide polymorphisms of the CX3CR1 gene (CX3CR1-V249I and CX3CR1-T280M) that disrupt the affinity of CX3CR1 for its natural ligand (fractalkine) could also affect the G glycoprotein-CX3CR1 pathway.

Methods: To test the hypothesis, DNA samples were obtained from 82 children hospitalized for RSV bronchiolitis in a 1-year period. One hundred twenty sex-matched healthy adults, without a history of severe lower respiratory tract infections, formed the control group.

Results: Epidemiologic data showed an increase in the RSV infection rate during the late winter season, with a peak rate in early spring. Genotyping revealed predominance of the 280M-containing genotypes (M/M or T/M) in cases compared with controls (37.8% versus 20.8%, respectively; odds ratio, 2.03; 95% confidence interval, 1.1-3.9; P = 0.025), demonstrating an association between the common CX3CR1-T280M variations and increased risk of severe RSV bronchiolitis.

Conclusions: Our findings support the hypothesis of the pivotal role of the G glycoprotein CX3CR1 pathway in the pathogenesis of RSV bronchiolitis and propose CX3CR1 as a potential therapeutic target.

MeSH terms

  • Bronchiolitis, Viral / epidemiology
  • Bronchiolitis, Viral / genetics*
  • Bronchiolitis, Viral / physiopathology*
  • Bronchiolitis, Viral / virology
  • CX3C Chemokine Receptor 1
  • Case-Control Studies
  • Chemokine CX3CL1
  • Chemokines, CX3C / metabolism
  • Female
  • Genetic Variation*
  • Humans
  • Infant
  • Male
  • Membrane Proteins / metabolism
  • Polymorphism, Single Nucleotide
  • Receptors, Cytokine / genetics*
  • Receptors, Cytokine / metabolism
  • Receptors, HIV / genetics*
  • Receptors, HIV / metabolism
  • Respiratory Syncytial Virus Infections / epidemiology
  • Respiratory Syncytial Virus Infections / genetics*
  • Respiratory Syncytial Virus Infections / physiopathology
  • Respiratory Syncytial Virus Infections / virology
  • Respiratory Syncytial Virus, Human / metabolism
  • Respiratory Syncytial Virus, Human / pathogenicity*
  • Risk Factors
  • Seasons
  • Severity of Illness Index

Substances

  • CX3C Chemokine Receptor 1
  • CX3CL1 protein, human
  • Chemokine CX3CL1
  • Chemokines, CX3C
  • Membrane Proteins
  • Receptors, Cytokine
  • Receptors, HIV