Division of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229, USA.
J Allergy Clin Immunol. 2010 Feb;125(2):469-476.e2. doi: 10.1016/j.jaci.2009.09.054.
The cytokine IL-9 has been implicated in allergic reactions, including food allergy, but its contribution to parenteral versus oral antigen-induced anaphylaxis remains unclear.
We sought to delineate the contribution of the IL-9/IL-9 receptor alpha-chain (IL-9R) pathway to parenteral and oral antigen-induced anaphylaxis.
Wild-type, IL-9-deficient (Il9(-/-)), and IL-9R-deficient (Il9R(-/-)) mice were subjected to passive and active parenteral and oral antigen (ovalbumin [OVA])-induced anaphylaxis. Severity of systemic anaphylaxis was gauged by decreased body temperature; intestinal anaphylaxis was assessed based on secretory diarrhea, intestinal mastocytosis, and serum murine mast cell protease 1 level. Specific immunoglobulin isotypes or immunoglobulin receptor-blocking antibodies were administered before challenge to define the role of the IgE and IgG pathways.
Repeated oral antigen challenge of OVA-sensitized wild-type mice induced anaphylaxis with both systemic and intestinal involvement; both were IgE dependent and attenuated in Il9(-/-) and Il9R(-/-) mice. In contrast, parenteral OVA challenge of OVA-sensitized wild-type mice induced systemic anaphylaxis, which was independent of the IL-9/IL-9R pathway. Strikingly, the IL-9/IL-9R pathway had no role in either the IgG or IgE component of parenteral antigen-induced or anti-IgE and anti-FcgammaRII/III mAb-induced systemic anaphylaxis.
Parenteral antigen-induced murine systemic anaphylaxis is mediated by both IgG- and IgE-dependent pathways, and both can occur independently of IL-9/IL-9R signaling. In contrast, oral antigen-induced intestinal and systemic anaphylaxis is strictly IgE mediated and requires IL-9/IL-9R signaling. These studies indicate differential involvement of the IL-9/IL-9R pathway in systemic and oral antigen-induced anaphylaxis.
细胞因子 IL-9 已被牵涉到过敏反应中,包括食物过敏,但它对肠外和口服抗原诱导的过敏反应的贡献尚不清楚。
我们试图阐明 IL-9/IL-9 受体α链(IL-9R)途径对肠外和口服抗原诱导的过敏反应的贡献。
野生型、IL-9 缺陷型(Il9(-/-))和 IL-9R 缺陷型(Il9R(-/-))小鼠接受被动和主动肠外和口服抗原(卵清蛋白[OVA])诱导的过敏反应。全身过敏反应的严重程度通过体温下降来衡量;肠过敏反应基于分泌性腹泻、肠肥大细胞和血清鼠肥大细胞蛋白酶 1 水平来评估。在挑战前给予特异性免疫球蛋白同种型或免疫球蛋白受体阻断抗体,以确定 IgE 和 IgG 途径的作用。
重复口服 OVA 致敏的野生型小鼠的 OVA 挑战会引起全身和肠道参与的过敏反应;两者均依赖 IgE,并在 Il9(-/-)和 Il9R(-/-)小鼠中减弱。相比之下,肠外 OVA 致敏的野生型小鼠的 OVA 挑战会引起全身过敏反应,该反应不依赖于 IL-9/IL-9R 途径。引人注目的是,IL-9/IL-9R 途径在肠外抗原诱导或抗 IgE 和抗 FcγRII/III mAb 诱导的全身过敏反应的 IgG 或 IgE 成分中均不起作用。
肠外抗原诱导的小鼠全身过敏反应是由 IgG 和 IgE 依赖性途径介导的,并且两者都可以独立于 IL-9/IL-9R 信号发生。相比之下,口服抗原诱导的肠道和全身过敏反应严格依赖 IgE,需要 IL-9/IL-9R 信号。这些研究表明,IL-9/IL-9R 途径在全身和口服抗原诱导的过敏反应中存在差异。