Clinical and Experimental Pediatrics
- 제45권7호
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- Pages.875-883
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- 2002
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- 2713-4148(eISSN)
기도 염증이 유발된 생쥐에서 CpG Oligodeoxynucleotides가 미치는 효과
Effect of CpG Oligodeoxynucleotides on Airways of Mice with Established Airways Inflammation
- 황혜원 (동국대학교 의과대학 소아과학교실) ;
- 김수진 (동국대학교 의과대학 소아과학교실) ;
- 김원덕 (동국대학교 의과대학 소아과학교실) ;
- 조성민 (동국대학교 의과대학 소아과학교실) ;
- 이동석 (동국대학교 의과대학 소아과학교실) ;
- 최성민 (동국대학교 의과대학 소아과학교실)
- Hwang, Hei-Won (Department of Pediatrics, College of Medicine, Dongguk University) ;
- Kim, Su-Jin (Department of Pediatrics, College of Medicine, Dongguk University) ;
- Kim, Won-Duk (Department of Pediatrics, College of Medicine, Dongguk University) ;
- Cho, Sung-Min (Department of Pediatrics, College of Medicine, Dongguk University) ;
- Lee, Dong-Suk (Department of Pediatrics, College of Medicine, Dongguk University) ;
- Choi, Sung-Min (Department of Pediatrics, College of Medicine, Dongguk University)
- 투고 : 2002.01.21
- 심사 : 2002.05.08
- 발행 : 2002.07.15
초록
목 적 : 기관지 천식은 Th2 반응 우세로 인한 기도의 호산구증과 IgE 증가를 특징으로 하는 질환이다. 박테리아 DNA 혹은 합성 ODNs인 unmethylated CpG motifs(CpG)은 Th1 사이토카인인
Purpose : Airways eosinophilia and increased IgE, characteristic features of asthma, result from a predominant Th2 response. In this study, we investigated the effect of CpG oligodeoxynucleotides (ODNs) on the inhibition of airways eosinophilia in mice with established airway inflammation. We also investigated the immunological mechanisms involved. Methods : Groups of BALB/c mice were sensitized intradermally with ovalbumin(OVA). At week 10, airway inflammation was induced by intranasal challenge of the mice with OVA. At week 14, the mice were challenged intranasally again with OVA in the presence and without the presence of CpG ODNs. Mice with saline administration served as negative controls. Bronchoalveolar lavage fluids(BALF) were obtained and eosinophils were counted. Th1 and Th2 cytokines in the spleen cell cultures were measured by ELISA. Serum OVA-specific IgE and IgG2a antibodies were also measured by ELISA. Results : BALF eosinophils were significantly inhibited in the CpG ODNs-treated mice(P<0.01). IgE and IgG2a levels increased significantly in both CpG ODNs-treated and untreated groups as compared to the negative control group; there was, however, no significant difference between the two groups four days after intranasal administration of CpG ODNs. Cytokine analysis revealed decreased production of IL-4, IL-5, and IL-13 and increased production of IL-12 in the CpG ODNs-treated group as compared to the untreated group. Interestingly,