Department of Otorhinolaryngology, Head and Neck Surgery, Inha University College of Medicine, Incheon, Korea.
Allergy. 2012 Feb;67(2):183-90. doi: 10.1111/j.1398-9995.2011.02735.x. Epub 2011 Nov 4.
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.
白细胞介素 (IL)-33 参与 Th2 免疫反应,在鼻过敏中可能发挥重要作用。因此,我们旨在研究抗-IL-33 治疗变应性鼻炎 (AR) 的潜力。
使用 24 只 BALB/c 小鼠。在 A 组(对照组,n = 6)中,小鼠用生理盐水致敏和激发。B 组 [卵清蛋白 (OVA) 组,n = 6] 小鼠接受腹腔和鼻腔 OVA 挑战。C 组(对照 IgG 组,n = 6),在 OVA 挑战前,小鼠接受腹腔注射兔对照 IgG。D 组(抗-IL-33 组,n = 6),在挑战前注射抗-IL-33。我们评估了抓鼻次数和外部形态;血清总 IgE 和 OVA 特异性 IgE;支气管肺泡灌洗液 (BAL) 中的嗜酸性粒细胞、中性粒细胞和淋巴细胞数;鼻腔组织病理学检查;和 BAL 液中的 IL-4、IL-5 和 IL-13。
抗-IL-33 治疗显著减少了抓鼻次数,改善了皮肤脱屑。D 组血清总 IgE 和 OVA 特异性 IgE 显著降低。BAL 液中的嗜酸性粒细胞数也显著减少。D 组鼻腔嗜酸性粒细胞浸润明显减少。BAL 液中的 IL-4、IL-5 和 IL-13 治疗后也显著降低。
抗-IL-33 抗体对实验性 AR 具有治疗潜力。