Shin Ji Hyeon, Kim Do Hyun, Kim Boo Young, Kim Sung Won, Hwang Se Hwan, Lee Joohyung, Kim Soo Whan
Department of Otolaryngology-Head and Neck Surgery, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Allergy Asthma Immunol Res. 2017 May;9(3):237-246. doi: 10.4168/aair.2017.9.3.237.
Interleukin (IL)-9 induces allergic responses; however, the roles of anti-IL-9 antibody in the induction of tolerance remain unclear. This study investigated the effects of anti-IL-9 antibody on oral tolerance (OT) in a mouse model of allergic rhinitis (AR).
BALB/c mice were divided into 4 groups: the control, AR, OT, and OT with anti-IL-9 antibody (OT+IL9AB) groups. Ovalbumin (OVA) was used for sensitization and challenge. Mice in the OT and OT+IL9AB groups were fed OVA for immunotherapy. During immunotherapy, OT+IL9AB mice were injected with anti-IL-9 antibody. Allergic symptoms, tissue eosinophil counts, and serum OVA-specific immunoglobulin E (IgE) were measured. The mRNA expressions of cytokines and transcription factors of T cells of nasal mucosa were determined by real-time polymerase chain reaction (PCR). The protein levels of GATA3, ROR-γt, and Foxp3 in nasal mucosa were determined by Western blot. CD4⁺CD25⁺Foxp3⁺ T cells in the spleen were analyzed by flow cytometry.
Administration of anti-IL-9 antibody decreased allergic symptoms, OVA-specific IgE levels, and eosinophil counts. In addition, it inhibited T-helper (Th) 2 responses, but had no effect on Th1 responses. Protein levels of ROR-γt and mRNA levels of PU.1 and ROR-γt were reduced by anti-IL-9 antibody. Anti-IL-9 antibody increased Foxp3 and IL-10 mRNA expression, Foxp3 protein, and induction of CD4⁺CD25⁺Foxp3⁺ T cells.
Anti-IL-9 antibody decreased allergic inflammation through suppression of Th2 and Th17 cells. Anti-IL-9 antibody enhanced the tolerogenic effects of regulatory T cells. These results suggest that anti-IL-9 antibody might represent a potential therapeutic agent for allergen immunotherapy in patients with uncontrolled allergic airway disease.
白细胞介素(IL)-9可诱导过敏反应;然而,抗IL-9抗体在诱导免疫耐受中的作用仍不清楚。本研究在变应性鼻炎(AR)小鼠模型中探讨了抗IL-9抗体对口服耐受(OT)的影响。
将BALB/c小鼠分为4组:对照组、AR组、OT组和抗IL-9抗体OT组(OT+IL9AB组)。用卵清蛋白(OVA)进行致敏和激发。OT组和OT+IL9AB组小鼠喂食OVA进行免疫治疗。在免疫治疗期间,给OT+IL9AB组小鼠注射抗IL-9抗体。测量过敏症状、组织嗜酸性粒细胞计数和血清OVA特异性免疫球蛋白E(IgE)。通过实时聚合酶链反应(PCR)测定鼻黏膜T细胞细胞因子和转录因子的mRNA表达。通过蛋白质免疫印迹法测定鼻黏膜中GATA3、ROR-γt和Foxp3的蛋白水平。通过流式细胞术分析脾脏中CD4⁺CD25⁺Foxp3⁺ T细胞。
给予抗IL-9抗体可减轻过敏症状、OVA特异性IgE水平和嗜酸性粒细胞计数。此外,它抑制辅助性T(Th)2反应,但对Th1反应无影响。抗IL-9抗体降低了ROR-γt的蛋白水平以及PU.1和ROR-γt的mRNA水平。抗IL-9抗体增加了Foxp3和IL-10的mRNA表达、Foxp3蛋白以及CD4⁺CD25⁺Foxp3⁺ T细胞的诱导。
抗IL-9抗体通过抑制Th2和Th17细胞减轻变应性炎症。抗IL-9抗体增强了调节性T细胞的致耐受性作用。这些结果表明,抗IL-9抗体可能是治疗未控制的变应性气道疾病患者变应原免疫治疗的一种潜在治疗药物。