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:Validation of DoriVac (DNA Origami Vaccine) Efficacy in a Metastatic Melanoma Model.
Validation of DoriVac (DNA Origami Vaccine) Efficacy in a Metastatic Melanoma Model.
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转移性癌症,尤其是转移性黑色素瘤,由于其对标准治疗的耐药性以及20-27%的低五年生存率,构成了重大的治疗挑战。癌症疫苗研究的最新进展在减少疾病复发方面显示出巨大前景,但这些方法仍面临抗原选择、生产便捷性和可编程性方面的挑战。为解决其中一些挑战,我们将DoriVac平台改造为针对转移性黑色素瘤的癌症疫苗。DoriVac是一种基于DNA折纸的疫苗平台,允许以最佳纳米间距共同递送所选抗原和CpG免疫佐剂,以促进Th1免疫极化。在我们的研究中,我们观察到在B16OVA和B16F10黑色素瘤模型中,DoriVac治疗的小鼠肺部肿瘤结节显著减少。DoriVac似乎也是一种安全的治疗方法,因为我们未观察到抗纳米颗粒(即抗dsDNA)抗体的任何显著增加。
重要的是,我们观察到当DoriVac与αPD-L1免疫检查点阻断联合使用时效果增强,导致转移性肺肿瘤结节进一步减少。我们的结果还表明,与对照组相比,抗原呈递细胞、NK细胞、CD4+ T细胞和CD8+ T细胞的激活增加。这些发现表明,DoriVac,特别是与αPD-L1免疫检查点阻断联合使用时,可作为对抗转移性癌症的有前景的免疫疗法。
Metastatic cancer, particularly metastatic melanoma, poses a significant therapeutic challenge due to its resistance to standard treatments and a low five-year survival rate of 20-27%. Recent advances in cancer vaccine research show great promise in reducing disease recurrence, but these approaches still face challenges pertaining to antigen selection, ease of production, and programmability. To address some of these challenges, we have adapted the DoriVac platform to serve as a cancer vaccine against metastatic melanoma.
DoriVac is a DNA origami-based vaccine platform that allows for the codelivery of antigens of choice and the CpG immune adjuvant at an optimal nanospacing to promote Th1 immune polarization. In our study, we observed a significant reduction in lung tumor nodules in the B16OVA and B16F10 melanoma models for DoriVac-treated mice. DoriVac also appears to be a safe treatment, as we did not observe any significant increase in antinanoparticle (i. e. , anti-dsDNA) antibodies.
Importantly, we observed an enhanced effect when DoriVac was combined with an αPD-L1 immune checkpoint blockade, leading to an even greater reduction in metastatic lung tumor nodules.
Our results also indicate an increased activation of antigen-presenting cells, NK cells, CD4 + T cells, and CD8 + T cells in comparison to the control groups.
These findings suggest that DoriVac, particularly in combination with the αPD-L1 immune checkpoint blockade, can serve as a promising immunotherapy against metastatic cancer.
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