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一种用于持续递送抗炎纳米载体并在动脉粥样硬化中诱导调节性T细胞的可注射水凝胶平台。

An Injectable Hydrogel Platform for Sustained Delivery of Anti-inflammatory Nanocarriers and Induction of Regulatory T Cells in Atherosclerosis.

作者信息

Yi Sijia, Karabin Nicholas B, Zhu Jennifer, Bobbala Sharan, Lyu Huijue, Li Sophia, Liu Yugang, Frey Molly, Vincent Michael, Scott Evan A

机构信息

Department of Biomedical Engineering, Northwestern University, Evanston, IL, United States.

出版信息

Front Bioeng Biotechnol. 2020 Jun 5;8:542. doi: 10.3389/fbioe.2020.00542. eCollection 2020.

Abstract

Chronic unresolved vascular inflammation is a critical factor in the development of atherosclerosis. Cardiovascular immunotherapy has therefore become a recent focus for treatment, with the objective to develop approaches that can suppress excessive inflammatory responses by modulating specific immune cell populations. A benefit of such immunomodulatory strategies is that low dosage stimulation of key immune cell populations, like antigen presenting cells, can subsequently propagate strong proliferation and therapeutic responses from effector cells. We have previously demonstrated that intravenous injections of anti-inflammatory nanocarriers provided atheroprotection that was mediated by regulatory T cells (Tregs) upregulated in lymphoid organs and atherosclerotic lesions. Here, we demonstrate an injectable filamentous hydrogel depot (FM-depot) engineered for low dosage, sustained delivery of anti-inflammatory nanocarriers. The bioactive form of vitamin D (aVD; 1, 25-Dihydroxyvitamin D3), which inhibits pro-inflammatory transcription factor NF-κB via the intracellular nuclear hormone receptor vitamin D receptor (VDR), was stably loaded into poly(ethylene glycol)-block-poly(propylene sulfide) (PEG--PPS) filomicelles. These aVD-loaded filaments underwent morphological transitions to release monodisperse drug-loaded micelles upon oxidation. This cylinder-to-micelle transition was characterized by cryogenic transmission electron microscopy (CryoTEM) and small angle X-ray scattering (SAXS). Following crosslinking with multi-arm PEG for gelation, aVD-loaded FM-depots maintained high levels of Foxp3 Tregs in both lymphoid organs and atherosclerotic lesions for weeks following a single subcutaneous injection into ApoE mice. FM-depots therefore present a customizable delivery platform to both develop and test nanomedicine-based approaches for anti-inflammatory cardiovascular immunotherapy.

摘要

慢性未解决的血管炎症是动脉粥样硬化发展的关键因素。因此,心血管免疫疗法已成为近期的治疗重点,目标是开发能够通过调节特定免疫细胞群体来抑制过度炎症反应的方法。这种免疫调节策略的一个好处是,低剂量刺激关键免疫细胞群体,如抗原呈递细胞,随后可以促进效应细胞的强烈增殖和治疗反应。我们之前已经证明,静脉注射抗炎纳米载体可提供动脉粥样硬化保护,这是由在淋巴器官和动脉粥样硬化病变中上调的调节性T细胞(Tregs)介导的。在这里,我们展示了一种可注射的丝状水凝胶贮库(FM贮库),其设计用于低剂量、持续递送抗炎纳米载体。维生素D的生物活性形式(aVD;1,25-二羟基维生素D3)通过细胞内核激素受体维生素D受体(VDR)抑制促炎转录因子NF-κB,被稳定地装载到聚(乙二醇)-嵌段-聚(硫化丙烯)(PEG-PPS)丝状胶束中。这些载有aVD的细丝在氧化后发生形态转变,释放出单分散的载药胶束。这种圆柱体到胶束的转变通过低温透射电子显微镜(CryoTEM)和小角X射线散射(SAXS)进行表征。在用多臂PEG交联以形成凝胶后,将载有aVD的FM贮库单次皮下注射到ApoE小鼠体内数周后,在淋巴器官和动脉粥样硬化病变中均维持了高水平的Foxp3 Tregs。因此,FM贮库提供了一个可定制的递送平台,用于开发和测试基于纳米医学的抗炎心血管免疫疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8313/7289959/48c16770e20d/fbioe-08-00542-g0001.jpg

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