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将氢氧化铝与 MF59 进行巧妙组合可诱导强烈的细胞免疫应答。

Smart combination of aluminum hydroxide and MF59 to induce strong cellular immune responses.

机构信息

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

出版信息

J Control Release. 2022 Sep;349:699-711. doi: 10.1016/j.jconrel.2022.07.032. Epub 2022 Jul 30.

Abstract

As two of the most widely used adjuvants, aluminum hydroxide and the oil-in-water emulsion MF59 have their intrinsic limitations: classical aluminum gel induces only weak cellular immune responses while MF59 cannot be used as an antigen delivery system due to its poor physical interaction with antigen molecules. Herein, we combined these two adjuvants and constructed a novel nano-vaccine delivery system by inserting aluminum hydroxide into the surface of a modified MF59 nano-emulsion (AlNEs). A model antigen ovalbumin (OVA) and an immune potentiator CpG were adsorbed on the surface of AlNEs (hereinafter AlNEs-OVA-CpG) through a facile mixing step. After subcutaneous injection, AlNEs-OVA-CpG effectively drained to lymph nodes, delivered both cargos into lymph node-resident antigen presenting cells (APCs), and escaped from lysosomes into the cytoplasm, resulting in enhanced antigen cross-presentation. Finally, AlNEs-OVA-CpG induced potent antigen-specific humoral and cellular immune responses, which significantly inhibited tumor growth and prolonged mice survival in a EG7-OVA tumor model. In sum, our results suggested that AlNEs have a great prospect to induce CD8 T cell responses for subunit antigens.

摘要

作为两种最广泛使用的佐剂,氢氧化铝和水包油乳剂 MF59 都有其内在的局限性:经典的铝凝胶仅诱导较弱的细胞免疫反应,而 MF59 由于与抗原分子的物理相互作用不佳,不能用作抗原递送系统。在此,我们将这两种佐剂结合起来,通过将氢氧化铝插入改良 MF59 纳米乳液(AlNEs)的表面,构建了一种新型的纳米疫苗递送系统。通过简单的混合步骤,将模型抗原卵清蛋白(OVA)和免疫增强剂 CpG 吸附在 AlNEs 的表面(以下称为 AlNEs-OVA-CpG)。皮下注射后,AlNEs-OVA-CpG 有效地引流到淋巴结,将两种载体递送至淋巴结驻留的抗原呈递细胞(APC),并从溶酶体逃逸到细胞质中,从而增强了抗原交叉呈递。最后,AlNEs-OVA-CpG 诱导了强烈的抗原特异性体液和细胞免疫反应,显著抑制了 EG7-OVA 肿瘤模型中的肿瘤生长并延长了小鼠的存活时间。总之,我们的结果表明,AlNEs 具有诱导亚单位抗原 CD8 T 细胞反应的巨大前景。

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