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利用诱导活性氧的还原氧化石墨烯纳米片实现个性化癌症疫苗的高效淋巴结靶向递送。

Efficient Lymph Node-Targeted Delivery of Personalized Cancer Vaccines with Reactive Oxygen Species-Inducing Reduced Graphene Oxide Nanosheets.

作者信息

Xu Cheng, Hong Hao, Lee Yonghyun, Park Kyung Soo, Sun Mingjiao, Wang Tianrui, Aikins Marisa E, Xu Yao, Moon James J

机构信息

Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan 48109, United States.

Biointerfaces Institute, University of Michigan, Ann Arbor, Michigan 48109, United States.

出版信息

ACS Nano. 2020 Oct 27;14(10):13268-13278. doi: 10.1021/acsnano.0c05062. Epub 2020 Sep 15.

Abstract

Therapeutic cancer vaccines require robust cellular immunity for the efficient killing of tumor cells, and recent advances in neoantigen discovery may provide safe and promising targets for cancer vaccines. However, elicitation of T cells with strong antitumor efficacy requires intricate multistep processes that have been difficult to attain with traditional vaccination approaches. Here, a multifunctional nanovaccine platform has been developed for direct delivery of neoantigens and adjuvants to lymph nodes (LNs) and highly efficient induction of neoantigen-specific T cell responses. A PEGylated reduced graphene oxide nanosheet (RGO-PEG, 20-30 nm in diameter) is a highly modular and biodegradable platform for facile preparation of neoantigen vaccines within 2 h. RGO-PEG exhibits rapid, efficient (15-20% ID/g), and sustained (up to 72 h) accumulation in LNs, achieving >100-fold improvement in LN-targeted delivery, compared with soluble vaccines. Moreover, RGO-PEG induces intracellular reactive oxygen species in dendritic cells, guiding antigen processing and presentation to T cells. Importantly, a single injection of RGO-PEG vaccine elicits potent neoantigen-specific T cell responses lasting up to 30 days and eradicates established MC-38 colon carcinoma. Further combination with anti-PD-1 therapy achieved great therapeutic improvements against B16F10 melanoma. RGO-PEG may serve a powerful delivery platform for personalized cancer vaccination.

摘要

治疗性癌症疫苗需要强大的细胞免疫来有效杀伤肿瘤细胞,而新抗原发现方面的最新进展可能为癌症疫苗提供安全且有前景的靶点。然而,引发具有强大抗肿瘤功效的T细胞需要复杂的多步骤过程,而传统疫苗接种方法很难实现这一点。在此,已开发出一种多功能纳米疫苗平台,用于将新抗原和佐剂直接递送至淋巴结(LN),并高效诱导新抗原特异性T细胞反应。聚乙二醇化还原氧化石墨烯纳米片(RGO-PEG,直径20-30纳米)是一种高度模块化且可生物降解的平台,可在2小时内轻松制备新抗原疫苗。与可溶性疫苗相比,RGO-PEG在淋巴结中表现出快速、高效(15-20%ID/g)且持续(长达72小时)的蓄积,实现了靶向淋巴结递送提高100倍以上。此外,RGO-PEG可在树突状细胞中诱导细胞内活性氧,引导抗原加工并呈递给T细胞。重要的是,单次注射RGO-PEG疫苗可引发持续长达30天的强大新抗原特异性T细胞反应,并根除已建立的MC-38结肠癌。进一步与抗PD-1疗法联合使用,对B16F10黑色素瘤的治疗取得了重大改善。RGO-PEG可能成为个性化癌症疫苗接种的强大递送平台。

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