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:Curing inflammatory diseases using phosphorous dendrimers.
Curing inflammatory diseases using phosphorous dendrimers.
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不同类型的可溶性磷树枝状聚合物已被合成,并显示出许多不同的生物学特性。尤其已经表明,第一代以氮杂双膦酸酯末端官能团修饰的磷树枝状聚合物能够在离体条件下刺激人体免疫系统。这些树枝状聚合物在几秒钟内被单核细胞内化,并诱导其抗炎激活。树枝状聚合物的存在还诱导抑制单核细胞向破骨细胞分化、树突状细胞成熟,并抑制促炎性 CD4+ T 淋巴细胞的增殖。
最后,在外周血单核细胞培养 2-3 周后,观察到NK 细胞扩增数十倍。鉴于所有这些特性,这些氮杂双膦酸酯树枝状聚合物的影响已在多种动物模型中进行了体内测试,针对不同的慢性或急性炎症性疾病,如多发性硬化症、类风湿性关节炎、葡萄膜炎和银屑病,但也针对髓系白血病,一种血液系统癌症。血液学安全性已在小鼠中得到证明,因为无血小板聚集、无溶血,且血液学指标无紊乱。氮杂双膦酸酯树枝状聚合物的安全性也在非人灵长类动物(食蟹猴)中进行了评估,这些动物接受了重复注射,作为降低风险的临床前测试。在整个研究过程中,外周血中的生化、血液学和所有免疫学参数均保持在正常生理范围内,且所有动物均存活良好。其他磷树枝状聚合物在体内也显示出抗炎特性,特别是用甘露糖衍生物功能化的树枝状聚合物,当口服(per os)给予小鼠时,可预防急性肺部疾病。本文归类于:生物学中的纳米技术方法 > 生物学中的纳米级系统;治疗方法和药物发现 > 新兴技术;治疗方法和药物发现 > 神经系统疾病的纳米医学。
Different types of water-soluble phosphorous dendrimers have been synthesized and display many different biological properties. It has been shown in particular that phosphorous dendrimers of first generation functionalized with azabisphosphonate terminal functions are able to stimulate the human immune system ex vivo.
These dendrimers are internalized by monocytes within a few seconds, and induce their anti-inflammatory activation. The presence of the dendrimers induces also the inhibition of the differentiation of monocytes into osteoclasts, the maturation of dendritic cells, and inhibits the proliferation of the proinflammatory CD4 + T lymphocytes.
Finally, after 2-3 weeks of culture of peripheral blood mononuclear cells, amplifications by several tens of natural killer cells is observed. In view of all these properties, the influence of these azabisphosphonate-dendrimers has been tested in vivo with several animal models, against different chronic or acute inflammatory diseases, such as multiple sclerosis, rheumatoid arthritis, uveitis, and psoriasis, but also against myeloid leukemia, a hematological cancer. The hematological safety has been demonstrated in mice, as there is no platelet aggregation, no hemolysis, and no disturbance in the hematological formula. The safety of the azabisphosphonate-dendrimer has been assessed also with non-human primates (cynomolgus monkeys) which received repeated injections, as a de-risking pre-clinical test.
Biochemical, hematological, and all immunological parameters in peripheral blood remained within a normal physiological range throughout the study, and all survived well. Other phosphorous dendrimers also display anti-inflammatory properties in vivo, in particular dendrimers functionalized with mannose derivatives, which prevent acute lung diseases when given orally (per os) to mice.
This article is categorized under: Nanotechnology Approaches to Biology > Nanoscale Systems in Biology Therapeutic Approaches and Drug Discovery > Emerging Technologies Therapeutic Approaches and Drug Discovery > Nanomedicine for Neurological Disease.
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