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:The TLR7/8 agonist R848 optimizes host and tumor immunity to improve therapeutic efficacy in murine lung cancer.
The TLR7/8 agonist R848 optimizes host and tumor immunity to improve therapeutic efficacy in murine lung cancer.
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Toll样受体7(TLR7)激动剂resiquimod(R848)治疗对多种类型的癌症有效,如乳腺癌、胰腺癌和结直肠癌。据报道,R848在肺癌中的抗肿瘤作用被认为是通过靶向巨噬细胞实现的。
在本研究中,证实了TLR7在多种免疫细胞类型上的表达在肺癌早期升高,然后在晚期下降。腹腔注射R848可减少C57BL/6小鼠皮下和转移性肺癌模型中的肿瘤负荷并延长生存期。发现在早期阶段初始使用R848治疗是最佳选择。全身注射R848促进了先天性和适应性免疫反应的激活。全身给予R848上调了树突状细胞(DCs)中TLR7的表达,并增强了DCs和自然杀伤(NK)细胞的激活。
此外,该治疗还导致血清中T辅助细胞相关细胞因子产生增加,包括IFN-γ、TNF-α和IL-2。此外,持续使用R848治疗增加了肿瘤微环境中DCs、NK和CD8+ T细胞的比例,并减少了Foxp3+调节性T细胞的比例。这些发现支持通过靶向TLR7使用R848治疗肺癌,并为潜在的治疗机制提供了见解。
Treatment with the Toll‑like receptor 7 (TLR7) agonist, resiquimod (R848), is effective in various types of cancer, such as breast, pancreatic and colorectal cancer. The reported antitumor effect of R848 in lung cancer is considered to be achieved by targeting macrophages. In the present study, it was demonstrated that TLR7 expression on various immune cell types initially rises, then declines in the late stage of lung cancer.
Intraperitoneal injection of R848 resulted in a reduction in tumor burden and prolonged survival in both subcutaneous and metastatic lung cancer models in C57BL/6 mice. Initial treatment with R848 at an early stage was found to be the optimal choice. Systemic injection of R848 promoted the activation of innate and adaptive immune responses. Systemic administration of R848 upregulated TLR7 expression in dendritic cells (DCs) and enhanced the activation of DCs and natural killer (NK) cells.
Moreover, this treatment also resulted in increased production of T helper cell‑associated cytokines in serum, including IFN‑γ, TNF‑α and IL‑2.
In addition, continuous treatment with R848 increased the proportion of DCs, NK and CD8 + T cells, and reduced that of Foxp3 + regulatory T cells in the tumor microenvironment.
These findings supported the use of R848 treatment for lung cancer via TLR7 targeting and provided insight into the underlying therapeutic mechanism.
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