纳米笼
免疫系统
癌症研究
抗原
佐剂
细胞毒性T细胞
癌症免疫疗法
抗原提呈细胞
CD8型
免疫疗法
材料科学
体内
免疫学
T细胞
生物
医学
体外
生物化学
生物技术
催化作用
作者
Ruijing Liang,Jun Xie,Jun Li,Ke Wang,Liping Liu,Yujie Gao,Mubashir Hussain,Guanxin Shen,Jintao Zhu,Juan Tao
出处
期刊:Biomaterials
[Elsevier BV]
日期:2017-09-26
卷期号:149: 41-50
被引量:156
标识
DOI:10.1016/j.biomaterials.2017.09.029
摘要
For nanovaccine-based cancer immunotherapy, dendritic cells (DCs) are one of the most powerful antigen presenting cells (APCs) that initiate and promote the maturation of antigen-specific cytotoxic T lymphocytes (e.g., CD8+ T cells) to induce the local and systemic antitumor immunity and further suppress the tumor metastasis and produce long-term protection against tumor. Thus, the activation and maturation of DCs is the prerequisite for efficient CD8+ T cell-based antitumor immune responses, which is considered as a primary and promising task for nanovaccine engineering. Herein, we introduce a versatile nanovaccine of liposomes-coated gold nanocages (Lipos-AuNCs) modified with DCs specific antibody aCD11c for targeted delivery of adjuvant MPLA and melanoma antigen peptide TRP2 to promote the activation and maturation of DCs, and enhance tumor specific T lymphocytes responses. Moreover, AuNCs accumulation and AuNCs-engulfed DCs migration to regional lymph nodes (RLNs) became real-time visualization through in vivo fluorescence and photoacoustic (PA) imaging to monitor the immunity process. In vivo experimental results demonstrated that the targeted antigen/adjuvants-loaded AuNCs exhibited enhanced antitumor immune response to inhibit tumor growth and metastasis in both B16-F10 prophylactic and lung metastasis models, which may act as a promising nanoplatform for antitumor immunotherapy and in vivo tracking.
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