Eosinophil cationic protein and chemokines in nasopharyngeal secretions of infants with respiratory syncytial virus (RSV) bronchiolitis and non-RSV bronchiolitis

被引:15
作者
Kim, Hyun Hee [1 ]
Lee, Mi Hee [1 ]
Lee, Joon Sung [1 ]
机构
[1] Catholic Univ Korea, Kangnam St Marys Hosp Coll Med, Dept Pediat, Seoul 137701, South Korea
关键词
respiratory syncytial viruses; bronchiolitis; nasopharyngeal secretion; body secretions; eosinophil cationic protein; RANTES; eotaxin; CCL; 11; chemokine;
D O I
10.3346/jkms.2007.22.1.37
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:37 / 42
页数:6
相关论文
共 21 条
[11]   Eosinophil cationic protein in infants with respiratory syncytial virus bronchiolitis: Predictive value for subsequent development of persistent wheezing [J].
Pifferi, M ;
Ragazzo, V ;
Caramella, D ;
Baldini, G .
PEDIATRIC PULMONOLOGY, 2001, 31 (06) :419-424
[12]   Measuring airway inflammation in asthma: Eosinophils and eosinophilic cationic protein in induced sputum compared with peripheral blood [J].
Pizzichini, E ;
Pizzichini, MMM ;
Efthimiadis, A ;
Dolovich, J ;
Hargreave, FE .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1997, 99 (04) :539-544
[13]   Cloning of the human eosinophil chemoattractant, eotaxin - Expression, receptor binding, and functional properties suggest a mechanism for the selective recruitment of eosinophils [J].
Ponath, PD ;
Qin, SX ;
Ringler, DJ ;
ClarkLewis, I ;
Wang, J ;
Kassam, N ;
Smith, H ;
Shi, XJ ;
Gonzalo, JA ;
Newman, W ;
GutierrezRamos, JC ;
Mackay, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (03) :604-612
[14]  
Rosi E, 2000, CLIN EXP ALLERGY, V30, P577
[15]   Respiratory syncytial virus infection results in airway hyperresponsiveness and enhanced airway sensitization to allergen [J].
Schwarze, J ;
Hamelmann, E ;
Bradley, KL ;
Takeda, K ;
Gelfand, EW .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (01) :226-233
[16]   Elevated cytokine concentrations in the nasopharyngeal and tracheal secretions of children with respiratory syncytial virus disease [J].
Sheeran, P ;
Jafri, H ;
Carubelli, C ;
Saavedra, J ;
Johnson, C ;
Krisher, K ;
Sánchez, PJ ;
Ramilo, O .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1999, 18 (02) :115-122
[17]  
Shields MD, 1999, CLIN EXP ALLERGY, V29, P1382
[18]   A comparison of cytokine responses in respiratory syncytial virus and influenza A infections in infants [J].
Sung, RYT ;
Hui, SHL ;
Wong, CK ;
Lam, CWK ;
Yin, J .
EUROPEAN JOURNAL OF PEDIATRICS, 2001, 160 (02) :117-122
[19]  
VENGE P, 1995, PEDIATR PULM, P34
[20]  
Wang S Z, 2000, Respirology, V5, P1, DOI 10.1046/j.1440-1843.2000.00219.x