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多功能 MXene 修饰的 GelMA 水凝胶负载缺氧诱导的间充质干细胞衍生的细胞外囊泡缓解小鼠变应性鼻炎。

Multifunctional MXene-modified GelMA hydrogel loaded with hypoxia-induced mesenchymal stem cells derived extracellular vesicles alleviates allergic rhinitis in mice.

机构信息

Department of otorhinolaryngology head and neck surgery, Second Hospital of Jilin University, Changchun, China.

Department of otorhinolaryngology head and neck surgery, Second Hospital of Jilin University, Changchun, China.

出版信息

Int J Biol Macromol. 2024 Nov;281(Pt 3):136485. doi: 10.1016/j.ijbiomac.2024.136485. Epub 2024 Oct 10.

Abstract

Allergic rhinitis (AR) has gained an increasing prevalence over the years, a more effective and safe treatment strategy need to be carried out. Hypoxia induced Mesenchymal stem cell derived extracellular vesicles (hEVs) have shown great therapeutic potential for AR, however, their low bioavailability through systemic administration decreased efficacy in clinical application. In the current study, an MXene-modified GelMA hydrogel was developed as a sustained release platform for hEVs. The hEVs-loaded MXene-modified GelMA hydrogel (hEVs@M-GelMA hydrogel) we prepared had rich porous structure, good hydrophilicity, biocompatibility and antibacterial properties, and showed significant inhibitory effect on the generation of reactive oxygen species in vitro. By using AR mice model, we verified that hEVs@M-GelMA hydrogel significantly alleviated AR symptoms, reduced local eosinophil infiltration, inhibited the intensity of nasal oxidative stress response, suppressed the production of OVA-sIgE in blood, decreased IL-4 secretion and promoted IL-10 and IFN-γ expression. This study provides a novel delivery platform for MSC-EVs-based AR therapy.

摘要

变应性鼻炎(AR)近年来发病率不断上升,需要采取更有效和安全的治疗策略。缺氧诱导的间充质干细胞衍生的细胞外囊泡(hEVs)在治疗 AR 方面显示出巨大的治疗潜力,但其通过全身给药的生物利用度低,降低了其在临床应用中的疗效。在本研究中,开发了一种 MXene 修饰的 GelMA 水凝胶作为 hEVs 的缓释平台。我们制备的负载 hEVs 的 MXene 修饰的 GelMA 水凝胶(hEVs@M-GelMA 水凝胶)具有丰富的多孔结构、良好的亲水性、生物相容性和抗菌性能,并在体外显示出对活性氧生成的显著抑制作用。通过使用 AR 小鼠模型,我们验证了 hEVs@M-GelMA 水凝胶显著缓解了 AR 症状,减少了局部嗜酸性粒细胞浸润,抑制了鼻氧化应激反应的强度,抑制了血液中 OVA-sIgE 的产生,减少了 IL-4 的分泌,并促进了 IL-10 和 IFN-γ 的表达。本研究为基于 MSC-EVs 的 AR 治疗提供了一种新的递送平台。

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