卵清蛋白
免疫球蛋白E
医学
免疫学
鼻腔给药
支气管肺泡灌洗
嗜酸性粒细胞
白细胞介素5
过敏
抗体
免疫系统
白细胞介素
哮喘
细胞因子
内科学
肺
作者
Young Hyo Kim,Ting Yang,C.‐S. Park,Sung‐Hoon Ahn,Byong-Kwan Son,Jeong Hee Kim,Dae Hyun Lim,Tae Young Jang
出处
期刊:Allergy
[Wiley]
日期:2011-11-04
卷期号:67 (2): 183-190
被引量:103
标识
DOI:10.1111/j.1398-9995.2011.02735.x
摘要
Interleukin (IL)-33 is involved in the Th2 immune response and could play an essential role in nasal allergy. Therefore, we aimed to investigate the therapeutic potential of anti-IL-33 for allergic rhinitis (AR).Twenty-four BALB/c mice were used. In group A (control group, n = 6), mice were sensitized and challenged with saline. Group B [ovalbumin (OVA) group, n = 6] mice received intraperitoneal and intranasal OVA challenge. In group C (control IgG group, n = 6), mice were injected intraperitoneally with rabbit control IgG before OVA challenge. In group D (anti-IL-33 group, n = 6), anti-IL-33 was injected before challenge. We evaluated the number of nose-scratching events and external morphology; serum total and OVA-specific IgE; number of eosinophils, neutrophils, and lymphocytes in bronchoalveolar lavage (BAL) fluid; histopathologic examination of nasal cavity; and IL-4, IL-5, and IL-13 in BAL fluid.Anti-IL-33 treatment significantly reduced the nose-scratching events and ameliorated skin denudation. Serum total and OVA-specific IgE was significantly decreased in group D. The number of eosinophils in BAL fluid was also significantly decreased. Eosinophilic infiltration in the nasal cavity was significantly decreased in group D. IL-4, IL-5, and IL-13 in BAL fluid were also significantly decreased after treatment.Anti-IL-33 antibody has a therapeutic potential for experimental AR.
科研通智能强力驱动
Strongly Powered by AbleSci AI