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:Programmed Remodeling of the Tumor Milieu to Enhance NK Cell Immunotherapy Combined with Chemotherapy for Pancreatic Cancer.
Programmed Remodeling of the Tumor Milieu to Enhance NK Cell Immunotherapy Combined with Chemotherapy for Pancreatic Cancer.
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基于自然杀伤(NK)细胞的过继免疫疗法在血液系统肿瘤的临床试验中已显示出令人鼓舞的治疗效果。然而,由于NK细胞向肿瘤组织的募集和浸润不足,实体瘤的治疗效果仍面临挑战。在此,设计了一种程序化纳米重塑剂(DAS@P/H/pp),用于重塑致密的物理基质屏障并纠正肿瘤环境中趋化因子的失调,从而增强NK细胞在肿瘤中的募集和浸润。DAS@P/H/pp由酸性肿瘤环境触发,导致电荷反转并随后释放透明质酸酶(HAase)。HAase有效降解细胞外基质,促进免疫调节分子和化疗药物递送至深部肿瘤组织。在胰腺癌小鼠模型中,这种纳米介导的肿瘤微环境程序化重塑策略在多重近红外-II荧光监测下显著增强了NK92细胞的募集及其杀伤肿瘤细胞的能力。
Natural killer (NK) cell-based adoptive immunotherapy has demonstrated encouraging therapeutic effects in clinical trials for hematological cancers.
However, the effectiveness of treatment for solid tumors remains a challenge due to insufficient recruitment and infiltration of NK cells into tumor tissues.
Herein, a programmed nanoremodeler (DAS@P/H/pp) is designed to remodel dense physical stromal barriers and for dysregulation of the chemokine of the tumor environment to enhance the recruitment and infiltration of NK cells in tumors. The DAS@P/H/pp is triggered by the acidic tumor environment, resulting in charge reversal and subsequent hyaluronidase (HAase) release.
HAase effectively degrades the extracellular matrix, promoting the delivery of immunoregulatory molecules and chemotherapy drugs into deep tumor tissues. In mouse models of pancreatic cancer, this nanomediated strategy for the programmed remodeling of the tumor microenvironment significantly boosts the recruitment of NK92 cells and their tumor cell-killing capabilities under the supervision of multiplexed near-infrared-II fluorescence.
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