J Korean Med Sci.  2007 Feb;22(1):37-42. 10.3346/jkms.2007.22.1.37.

Eosinophil Cationic Protein and Chemokines in Nasopharyngeal Secretions of Infants with Respiratory Syncytial Virus (RSV) Bronchiolitis and Non-RSV Bronchiolitis

Affiliations
  • 1Department of Pediatrics, Kangnam St. Mary's Hospital College of Medicine, The Catholic University of Korea, Seoul, Korea. jslee@catholic.ac.kr

Abstract

Bronchiolitis is a risk factor for the development of childhood asthma. Eosinophilic inflammation in airways plays an important role in the pathophysiology of both bronchiolitis and asthma. To investigate this inflammation, we measured the eosinophil cationic protein (ECP), regulated on activation normal T-cell expressed and secreted (RANTES) and eotaxin levels in nasopharyngeal secretions (NPS). Twenty-eight patients with RSV bronchiolitis (RSV group), 11 patients with non-RSV bronchiolitis (non-RSV group) and 7 controls were enrolled in this study. ECP, RANTES, and eotaxin levels were measured by enzyme immunoassays. The ECP level in the NPS of the RSV group was significantly higher than that in the NPS of the non-RSV group and controls. RANTES and eotaxin levels in infants with bronchiolitis were significantly higher than those in the controls, but there was no significant difference between the RSV and non-RSV groups. In conclusion, with regard to eosinophilic airway inflammation, as compared with non-RSV bronchiolitis, RSV bronchiolitis may be more similar to childhood asthma.

Keyword

Respiratory Syncytial Viruses; Bronchiolitis; Nasopharyngeal Secretion; Body Secretions; Eosinophil Cationic Protein; RANTES; Eotaxin; CCL11 chemokine

MeSH Terms

Respiratory Syncytial Virus Infections/*immunology
RANTES/analysis
Nasopharynx/*immunology/secretion
Male
Infant
Humans
Female
Eosinophil Cationic Protein/*analysis
Chemokines, CC/analysis
Chemokines/*analysis
Bronchiolitis/*immunology

Figure

  • Fig. 1 ECP levels in nasopharyngeal secretion are significantly different between group (p<0.05). RSV (+), RSV bronchiolitis; RSV (-), non-RSV bronchiolitis.

  • Fig. 2 RANTES levels in nasopharyngeal secretion of infants with RSV bronchiolitis are significantly higher than those of controls (p<0.05). RSV (+), RSV bronchiolitis; RSV(-), non-RSV bronchiolitis.

  • Fig. 3 Eotaxin levels in nasopharyngeal secretion of infants with RSV bronchiolitis as well as those of infants with non-RSV bronchiolitis are significantly higher than those of controls (p<0.05). RSV (+), RSV bronchiolitis; RSV (-), non-RSV bronchiolitis.

  • Fig. 4 ECP level in nasopharyngeal secretion of infants with RSV bronchiolitis show highly correlated with eotaxin level (p=0.02, r=0.562) than with RANTES level (p=0.0497, r=0.36).

  • Fig. 5 RANTES and eotaxin levels in nasopharyngeal secretion of infants with RSV bronchiolitis show significant correlation (r=0.4392, p=0.039).


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