MOV纳米粒的构建及其通过恢复气道免疫调节功能改善气道过敏性疾病的作用OA
Construction of MOV nanoparticles to improve allergic airway diseases by restoring airway immunomodulatory function
目的 构建一种可恢复气道免疫调节功能的纳米粒,并评价其对气道过敏性炎症的免疫调控作用.方法 采用双乳化法制备负载血管活性肠肽(VIP)的纳米粒(VIP NPs),并利用MHC-Ⅱ/OVA表位肽融合蛋白修饰形成MOV纳米粒(MOV NPs),表征其理化性质及体外释放特性.在卵清蛋白(OVA)诱导的小鼠气道过敏模型中,给予不同剂量MOV NPs,检测血清特异性抗体、肺泡灌洗液(BALF)炎性介质和Th2细胞因子水平,结合流式细胞术与功能实验分析气道组织调节性T细胞(Tregs)的数量及功能,并检测Tregs相关因子转化生长因子-β(TGF-β)和白细胞介素-10(IL-10)的表达.结果 MOV NPs呈规则球形,具有负电位、稳定缓释特性,VIP包封率为(63.12±2.15)%.MOV NPs能降低血清sIgG1、sIgE水平及BALF中炎性介质和Th2细胞因子含量,并呈剂量依赖性效应.与模型组相比,MOV NPs可提升气道Tregs的数量及免疫抑制功能,并上调其TGF-β和IL-10表达水平.结论 MOV NPs兼具抗原递呈与VIP免疫调控双重作用,可有效抑制气道过敏性炎症并恢复局部免疫稳态.
Objective To construct a nanoparticle-based carrier capable of restoring airway immunoregulatory function under allergic conditions,and evaluate its immunomodulatory effects and potential therapeutic value against allergic airway inflammation.Methods Vasoactive intestinal peptide(VIP)-loaded nanoparticles(VIP NPs)were prepared using a double-emulsion method and further modified with an MHC-Ⅱ/OVA epitope peptide fusion protein to generate MOV nanoparticles(MOV NPs).The physicochemical properties and in vitro release profile of MOV NPs were characterized.An ovalbumin(OVA)-induced murine model of allergic airway disease was established and treated with different doses of MOV NPs.Serum allergen-specific antibodies,inflammatory mediators and Th2 cytokines in bronchoalveolar lavage fluid(BALF)were measured.Flow cytometry and functional assays were performed to analyze the abundance and suppressive activity of regulatory T cells(Tregs)in airway tissues.The expression levels of Treg-associated cytokines,transforming growth factor-β(TGF-β)and interleukin-10(IL-10)were further determined.Results MOV NPs exhibited a uniform spherical morphology,negative surface charge,stable sustained-release properties,and a VIP encapsulation efficiency of(63.12±2.15)%.MOV NPs treatment significantly reduced serum sIgG1 and sIgE levels,as well as BALF inflammatory mediators and Th2 type cytokines,in a dose-dependent manner.Compared with the model group,MOV NPs markedly increased the number and immunosuppressive function of airway Tregs,and up-regulated the expression levels of TGF-β and IL-10.Conclusion MOV NPs integrate dual functions of antigen presentation and VIP-mediated immunoregulation,which can effectively inhibit airway allergic inflammation and restore local immune homeostasis.
莫丽华;胡宇琴;杨锦娜;罗向前
南方医科大学深圳医院儿童耳鼻喉科,广东 深圳 518055南方医科大学深圳医院儿童耳鼻喉科,广东 深圳 518055南方医科大学深圳医院儿童耳鼻喉科,广东 深圳 518055南方医科大学深圳医院儿童耳鼻喉科,广东 深圳 518055
MOV纳米粒血管活性肠肽调节性T细胞免疫调控气道过敏性疾病
MOV nanoparticlesVasoactive intestinal peptideRegulatory T cellsImmune homeostasisAllergic airway disease
《新医学》 2026 (2)
139-148,10
广东省基础与应用基础研究基金(2023A1515030299)深圳市科技计划资助项目(JCYJ20220530154013030,JCYJ20240813145213018)南方医科大学深圳医院院内基金腾飞计划项目(22H3ATF04)
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