Zhong Yiwei, Su Caixia, Wu Shuting, Miao Chunhui, Wang Bin
Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS), Shanghai Frontiers Science Center of Pathogenic Microorganisms and Infection, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai, China; Fudan-Advaccine Join-Lab for Vaccine Research, Fudan University, Shanghai, China; Shanghai Institute of Infectious Disease and Biosecurity, Fudan University, Shanghai, China.
Advaccine Biopharmaceutics (Suzhou) Co. Ltd, Suzhou, Jiangsu Province, China.
Int Immunopharmacol. 2023 Mar;116:109718. doi: 10.1016/j.intimp.2023.109718. Epub 2023 Feb 2.
Asthma poses a significant threat to public health, with an estimated burden of over 334 million people worldwide. Available treatments are often inadequate. We developed a thermo-sensitive hydrogel vaccine containing allergen and FK506 that induced immune tolerance via intranasal administration to treat experimental allergic asthma. The hydrogel delivery system was formulated based on Poloxamer 407 (P407), Carbopol 974P NF, and Polyoxyl 15 hydroxystearate (Kolliphor HS15, HS15). It flowed freely at room temperature and rapidly formed a hydrogel in the nasal cavity once the temperature rose over 33 °C. Ovalbumin and FK506 were slowly released from the hydrogel form and their mucosal residence time was significantly prolonged compared to the liquid formulation. In both an OVA-induced asthma model and an HDM-induced asthma model, the vaccines formulated in hydrogel gave lower levels of eosinophilic inflammation, and airway remodeling. The reduction of lung function was ameliorated, and Foxp3-expressing CD4 + Treg cells were significantly higher. The frequency of Foxp3 + Tregs in lung-draining lymph nodes (dLNs) was correlated with the amelioration. Depletion of Foxp3 + Treg cells abolished the beneficial effects of the allergen/FK506 hydrogel vaccinations. Thus, the allergen/FK506 hydrogel formulation has the potential to be a delivery system for therapeutic allergy vaccines to induce immune tolerance.
哮喘对公众健康构成重大威胁,全球估计负担超过3.34亿人。现有的治疗方法往往不足。我们开发了一种含有变应原和FK506的热敏水凝胶疫苗,通过鼻内给药诱导免疫耐受,以治疗实验性过敏性哮喘。水凝胶递送系统是基于泊洛沙姆407(P407)、卡波姆974P NF和聚氧乙烯15羟基硬脂酸酯(聚氧乙烯氢化蓖麻油HS15,HS15)配制的。它在室温下自由流动,一旦温度超过33°C,就在鼻腔内迅速形成水凝胶。卵清蛋白和FK506从水凝胶形式中缓慢释放,与液体制剂相比,它们在粘膜中的停留时间显著延长。在卵清蛋白诱导的哮喘模型和屋尘螨诱导的哮喘模型中,水凝胶配制的疫苗产生的嗜酸性粒细胞炎症和气道重塑水平较低。肺功能的降低得到改善,表达Foxp3的CD4 + T调节细胞显著增多。肺引流淋巴结(dLNs)中Foxp3 + Tregs的频率与改善情况相关。去除Foxp3 + T调节细胞消除了变应原/FK506水凝胶疫苗接种的有益效果。因此,变应原/FK506水凝胶制剂有可能成为一种治疗性过敏疫苗的递送系统,以诱导免疫耐受。