알레르기 비염 환자에서 비유발시험 후 비즙내 특이 IgA와 호산구 활성화의 상관관계
DC Field | Value | Language |
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dc.contributor.advisor | 박해심 | - |
dc.contributor.author | 오정훈 | - |
dc.date.accessioned | 2019-10-21T06:46:00Z | - |
dc.date.available | 2019-10-21T06:46:00Z | - |
dc.date.issued | 2006-08 | - |
dc.identifier.other | 1616 | - |
dc.identifier.uri | https://dspace.ajou.ac.kr/handle/2018.oak/16367 | - |
dc.description | 학위논문(박사)--아주대학교 일반대학원 :의학과,2006. 8 | - |
dc.description.tableofcontents | ABSTRACT i TABLE OF CONTENTS iv LIST OF FIGURES vi LIST OF TABLES vii Ⅰ. INTRODUCTION 1 Ⅱ. MATERIALS AND METHODS 3 A. Subjects 3 B. Nasal allergen provocation 3 C. Evaluation of symptom score and acoustic rhinometry 4 D. Nasal lavage and inflammatory cells 4 E. Measurement of allergen-specific IgE 5 F. Measurement of allergen-specific IgG 6 G. Measurement of allergen-specific IgA 6 H. Measurement of total IgE and ECP 7 I. Statistical analyses 7 Ⅲ. RESULTS 8 A. Clinical characteristics of allergic rhinitis subjects and controls 8 B. Nasal symptom scores and acoustic rhinometry 9 C. Inflammatory cell counts and ECP levels in nasal lavage fluids 12 D. Total and specific immunoglobulins in nasal lavage fluids 16 E. Correlation between ECP and specific antibodies 20 F. ELISA inhibition results for specific antibodies 21 Ⅳ. DISCUSSION 22 Ⅴ. CONCLUSION 28 REFERENCES 29 국문요약 36 | - |
dc.language.iso | eng | - |
dc.publisher | The Graduate School, Ajou University | - |
dc.rights | 아주대학교 논문은 저작권에 의해 보호받습니다. | - |
dc.title | 알레르기 비염 환자에서 비유발시험 후 비즙내 특이 IgA와 호산구 활성화의 상관관계 | - |
dc.title.alternative | Jeong-Hoon Oh | - |
dc.type | Thesis | - |
dc.contributor.affiliation | 아주대학교 일반대학원 | - |
dc.contributor.alternativeName | Jeong-Hoon Oh | - |
dc.contributor.department | 일반대학원 의학과 | - |
dc.date.awarded | 2006. 8 | - |
dc.description.degree | Master | - |
dc.identifier.localId | 565541 | - |
dc.identifier.url | http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000001616 | - |
dc.subject.keyword | allergic rhinitis | - |
dc.subject.keyword | late response | - |
dc.subject.keyword | specific antibody | - |
dc.description.alternativeAbstract | Background: Eosinophils are the major effector cells in nasal allergic inflammation. However, the mechanism of eosinophil activation mediated by a series of inflammatory mediators presenting in early and late responses of allergic rhinitis (AR) is not fully understood. Objective: The aim of this study was to evaluate the role of locally produced allergen specific antibodies in the nasal lavage fluid during the recruitment of inflammatory cells in AR. Methods: Thirteen patients diagnosed with AR induced by sensitivity to Dermatophagoides pteronyssinus (Dp) according to positive responses to nasal provocation tests were enrolled in this study (positive group). Ten asymptomatic, sensitized subjects were enrolled as the control group. Of the positive responders, early (N = 7) and dual (N = 6) responders were categorized according to the presence of increased eosinophil counts 3 to 24 h after provocation. Nasal provocation tests were preformed with Dp-soaked paper disks, and nasal lavage fluids were collected before provocation and at 10, 30, and 60 min and 3, 6, and 24 h after the provocation test. The changes in symptoms were assessed with scores and acoustic rhinometry. Inflammatory cells, including eosinophils, were counted in the nasal lavage fluid. Eosinophil cationic protein (ECP), considered an active marker of inflammation, was measured by the CAP system. Specific IgE, IgG, and IgA antibodies to Dp were measured by ELISA. Results: Eosinophil counts were significantly increased in the positive group compared with the control group at baseline. After nasal provocation tests, eosinophil counts continuously increased with a peak at 1 h, and the increased numbers persisted until 24 h in the positive group. Eosinophil counts at baseline and at 1 to 24 h after nasal provocation were significantly higher in dual responders than in early responders. Specific IgA levels were increased after provocation in both the early and late responses of the positive group, and statistical significance was noted at 10 min and 3 h. There were no significant differences in specific IgE and IgG levels during nasal provocation between the two groups. Significant correlations were observed between specific IgA and ECP levels at baseline and 10 min, and between 6 h and 24 h after nasal provocation (r = 0.58, p = 0.004; r = 0.81, p < 0.0001; r = 0.46, p < 0.023; and r = 0.61, p = 0.02). Conclusion: Eosinophils act as major effector cells in both the early and late responses after allergen exposure in perennial allergic rhinitis. Locally produced allergen-specific IgA, but not specific IgE or IgG, in nasal mucosa may be involved in eosinophil activation in both the early and late responses. | - |
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