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:Focused acoustic vortex-mediated sonochemotherapy for the amplification of immunogenic cell death combined with checkpoint blockade to potentiate cancer immunotherapy.
Focused acoustic vortex-mediated sonochemotherapy for the amplification of immunogenic cell death combined with checkpoint blockade to potentiate cancer immunotherapy.
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声动力疗法(SDT)作为癌症免疫治疗的辅助手段,可增强全身抗肿瘤免疫。然而,基于传统聚焦超声(FUS)的SDT介导免疫治疗效率受到FUS微小聚焦区域的限制。聚焦声涡旋(FAV)具有更大的聚焦区域,在相同参数下可诱导比FUS更强的空化和热效应,有望克服这一问题。
本研究探讨了FAV介导的声化疗联合免疫检查点阻断(ICB)重塑免疫抑制性肿瘤微环境(TME)、抑制肿瘤生长和肺转移的可行性。将声敏剂二氢卟吩e6(Ce6)和化疗药物多柔比星(Dox)共载入微泡-脂质体复合物中,构建Ce6/Dox@Lip@MBs(CDLM),用于“一体化”协同声化疗,其主要成分均已获临床批准。与FUS激活的CDLM相比,FAV激活的CDLM显著富集了肿瘤中的免疫原性细胞死亡(ICD)诱导剂,并放大了癌细胞的ICD。
此外,放大ICD联合ICB增加了细胞毒性T淋巴细胞和NK 细胞的浸润,将M2巨噬细胞极化为M1巨噬细胞,并减少了调节性T细胞。
本研究提供了一种多功能策略,用于在肿瘤中富集ICD诱导剂并放大ICD,以改善免疫抑制性TME并增强全身抗肿瘤免疫。
Sonodynamic therapy (SDT) as an auxiliary modality of cancer immunotherapy enhances systemic anti-tumor immunity.
However, the efficiency of SDT-mediated immunotherapy based on conventional focused ultrasound (FUS) is restricted by the tiny focal region of FUS. Focused acoustic vortex (FAV) possessing a larger focal region, can induce stronger cavitation and thermal effects than FUS with the same parameters, having the potential to overcome this issue. This research investigated the feasibility of FAV-mediated sonochemotherapy combined with the immune checkpoint blockade (ICB) to reshape immunosuppressive tumor microenvironment (TME), inhibit tumor growth and lung metastasis.
Sonosensitizer chlorin e6 (Ce6) and chemotherapeutic agent doxorubicin (Dox) were co-loaded into microbubble-liposome complex to compose Ce6/Dox@Lip@MBs (CDLM) for "all-in-one" synergistic sonochemotherapy, whose main components were clinical approved. FAV-activated CDLM significantly enriched immunogenic cell death (ICD) inducers in tumors and amplified ICD of cancer cells compared with FUS-activated CDLM.
Furthermore, the amplified-ICD combined with ICB increased the infiltration of cytotoxic T lymphocytes and natural killer cells, polarized M2 macrophages to M1 macrophages, and decreased regulatory T cells.
This study provides a multifunctional strategy for enriching ICD inducers in tumors and amplifying ICD to ameliorate immunosuppressive TME and potentiate systemic anti-tumor immunity.
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