RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Galloylated Toll-Like Receptor 7/8 Agonist Nanovaccine for Enhanced Tumor Antigen Delivery in Personalized Immunotherapy.
Galloylated Toll-Like Receptor 7/8 Agonist Nanovaccine for Enhanced Tumor Antigen Delivery in Personalized Immunotherapy.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
癌症疫苗作为癌症免疫治疗中的一项关键技术,已展现出巨大的治疗潜力。然而,基于肿瘤细胞裂解物(TCLs)的传统疫苗由于免疫原性低、体内不稳定以及无法与佐剂共递送,在早期临床试验中结果令人失望。为解决这些问题,我们通过用没食子酸修饰toll样受体7/8(TLR7/8)激动剂R848,开发了一种纳米颗粒疫苗R848-GA@TCLs。该纳米疫苗利用没食子酰基部分的“捕获”能力共载TCLs和R848,形成稳定的纳米颗粒。R848-GA@TCLs高效靶向淋巴结,使TCL积累增加10倍,并能够在树突状细胞(DCs)内同步释放抗原和佐剂。
我们的结果表明,R848-GA@TCLs增加了肿瘤抗原的交叉呈递,促进促炎细胞因子的产生,并激活DCs,导致效应T细胞、自然杀伤(NK)细胞和M1巨噬细胞显著增加。这种强烈的免疫反应产生了强效的抗肿瘤效果,R848-GA@TCLs通过显著抑制肿瘤生长和转移,在多种肿瘤模型中显示出疗效。
总之,R848-GA@TCLs代表一种能够共递送TCLs和佐剂的个性化癌症疫苗,引发强效抗肿瘤免疫反应,并具有巨大的临床应用潜力。
Cancer vaccines, a critical technology in cancer immunotherapy, have shown great therapeutic potential.
However, traditional vaccines based on tumor cell lysates (TCLs) have shown disappointing results in early clinical trials due to low immunogenicity, in vivo instability, and the inability to codeliver with adjuvants. To address these issues, we developed a nanoparticle vaccine, R848-GA@TCLs, by modifying the toll-like receptor 7/8 (TLR7/8) agonist R848 with gallic acid.
This nanovaccine leverages the "capturing" ability of the galloyl moiety to coload TCLs and R848, forming stable nanoparticles. R848-GA@TCLs efficiently target lymph nodes, increasing TCL accumulation 10-fold, and enable the synchronized release of antigens and adjuvants within dendritic cells (DCs).
Our results show that R848-GA@TCLs increase with respect to the cross-presentation of tumor antigens, promote the production of pro-inflammatory cytokines, and activate DCs, leading to a significant increase in effector T cells, natural killer (NK) cells, and M1 macrophages. This strong immune response resulted in potent antitumor effects, with R848-GA@TCLs demonstrating efficacy in multiple tumor models by significantly inhibiting tumor growth and metastasis.
In conclusion, R848-GA@TCLs represent a personalized cancer vaccine capable of codelivering TCLs and adjuvants, eliciting robust antitumor immune responses, and hold great potential for clinical applications.
MEMBER ACCOUNT
登录成功会直接打开下一页。