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:Eosinophil-lymphocyte interactions in the tumor microenvironment and cancer immunotherapy.
Eosinophil-lymphocyte interactions in the tumor microenvironment and cancer immunotherapy.
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嗜酸性粒细胞是过敏性疾病中的重要效应细胞和治疗靶点。新出现的数据表明,嗜酸性粒细胞浸润多种实体瘤类型,并至少通过两种非互斥机制发挥多效性活性:与肿瘤细胞的直接相互作用,以及与淋巴细胞的复杂交叉对话。鉴于癌症治疗中免疫检查点抑制的革命性进展,我们综述了肿瘤微环境中嗜酸性粒细胞与淋巴细胞的相互作用。我们还分析了嗜酸性粒细胞与淋巴细胞亚群之间潜在的相互作用,包括 T 细胞、NK 细胞和固有淋巴细胞。我们提供了关于这些相互作用后果的观点,以及嗜酸性粒细胞如何作为辅助细胞影响对各种形式的 T 细胞介导免疫疗法的反应,并可能成为改善癌症免疫治疗的治疗靶点。
Eosinophils are important effector cells and therapeutic targets in allergic diseases. Emerging data indicate that eosinophils infiltrate a variety of solid tumor types and have pleiotropic activities by at least two non-mutually exclusive mechanisms: direct interactions with tumor cells, and intricate cross-talk with lymphocytes. In light of the immune checkpoint inhibition revolution in cancer therapy, we review eosinophil-lymphocyte interactions in the tumor microenvironment.
We also analyze potential interactions between eosinophils and lymphocyte subsets, including T cells, natural killer cells and innate lymphoid cells.
We provide perspectives on the consequences of these interactions and how eosinophils are accessory cells that can affect the response to various forms of T cell-mediated immunotherapies and might be therapeutically targeted to improve cancer immunotherapy.
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