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采用一锅法制备甘露聚糖包裹的过敏原纳米颗粒进行安全有效的口服过敏免疫治疗。

Safe and efficient oral allergy immunotherapy using one-pot-prepared mannan-coated allergen nanoparticles.

机构信息

Graduate School of Systems Life Sciences, Kyushu University, Fukuoka, 819-0395, Japan.

Division of Biochemistry, Graduate School of Pharmaceutical Sciences, Keio University, Tokyo, 105-8512, Japan.

出版信息

Biomaterials. 2023 Dec;303:122381. doi: 10.1016/j.biomaterials.2023.122381. Epub 2023 Oct 31.

DOI:10.1016/j.biomaterials.2023.122381
PMID:37935073
Abstract

Allergen immunotherapy (AIT) is the only curative treatment for allergic diseases. However, AIT has many disadvantages related to efficiency, safety, long-term duration, and patient compliance. Dendritic cells (DCs) have an important role in antigen-specific tolerance induction; thus, DC-targeting strategies to treat allergies such as glutaraldehyde crosslinked antigen to mannoprotein (MAN) have been established. However, glutaraldehyde crosslinking may reduce the antigen presentation efficiency of DCs. To overcome this, we developed a MAN-coated ovalbumin (OVA) nanoparticle (MDO), which uses intermolecular disulfide bond to crosslink OVA and MAN. MDO effectively targeted DCs resulting in tolerogenic DCs, and promoted higher antigen presentation efficiency by DCs compared with OVA or glutaraldehyde crosslinked nanoparticles. In vitro and in vivo experiments showed that DCs exposed to MDO induced T cells. Moreover, MDO had low reactivity with anti-OVA antibodies and did not induce anaphylaxis in allergic mice, demonstrating its high safety profile. In a mouse model of allergic asthma, MDO had significant preventative and therapeutic effects when administered orally or subcutaneously. Therefore, MDO represents a promising new approach for the efficient and safe treatment of allergies.

摘要

变应原免疫治疗(AIT)是治疗过敏性疾病的唯一方法。然而,AIT 存在许多缺点,包括效率、安全性、长期持续时间和患者依从性等方面的问题。树突状细胞(DC)在抗原特异性耐受诱导中具有重要作用;因此,已经建立了针对过敏的树突状细胞靶向治疗策略,例如戊二醛交联抗原至甘露糖蛋白(MAN)。然而,戊二醛交联可能会降低 DC 的抗原呈递效率。为了克服这一问题,我们开发了一种 MAN 包被的卵清蛋白(OVA)纳米颗粒(MDO),该纳米颗粒使用分子间二硫键将 OVA 和 MAN 交联。MDO 可以有效地靶向 DC,诱导产生耐受性 DC,并通过 DC 促进更高的抗原呈递效率,与 OVA 或戊二醛交联的纳米颗粒相比。体外和体内实验表明,暴露于 MDO 的 DC 诱导 T 细胞。此外,MDO 与抗 OVA 抗体的反应性较低,并且不会在过敏小鼠中引起过敏反应,表明其具有较高的安全性。在过敏性哮喘的小鼠模型中,MDO 经口服或皮下给药具有显著的预防和治疗作用。因此,MDO 为高效和安全地治疗过敏提供了一种有前途的新方法。

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