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:Potentiation of natural killer cells to overcome cancer resistance to NK cell-based therapy and to enhance antibody-based immunotherapy.
Potentiation of natural killer cells to overcome cancer resistance to NK cell-based therapy and to enhance antibody-based immunotherapy.
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自然杀伤(NK)细胞是先天免疫系统的细胞成分,能够识别并抑制癌细胞增殖。NK细胞可通过直接裂解(释放穿孔素和颗粒酶)或抗体依赖性细胞介导的细胞毒作用(ADCC)清除癌细胞。ADCC过程中,NK细胞表面的Fcγ受体IIIa(CD16)与已结合癌细胞的抗体恒定区结合。癌细胞可利用多种机制逃避NK细胞的抗肿瘤作用,包括抑制性细胞因子积聚、募集并扩增髓系来源抑制细胞(MDSC)和调节性T细胞(Treg)等免疫抑制细胞,以及调节NK细胞受体配体。为增强NK细胞抗肿瘤活性、克服癌细胞对NK细胞的耐受,研究者开发了多种策略。
工程化并增强NK细胞细胞毒性的三种主要策略包括:使用调节性细胞因子增强NK细胞功能、过继NK细胞治疗,以及采用工程化NK细胞增强抗体免疫治疗。尽管前两种策略提高了NK细胞治疗疗效,但仍存在免疫相关不良事件、诱导免疫抑制细胞及癌细胞进一步耐受NK细胞杀伤等局限。克服这些问题的一种策略,是联合可介导ADCC的单克隆抗体(mAb)和抗癌活性增强的工程化NK细胞。具有ADCC活性的mAb既能激活NK细胞,也有助于免疫效应细胞在肿瘤微环境(TME)中积聚。多项临床试验报告,工程化NK细胞联合具有ADCC活性的mAb,临床应答优于单用mAb。下一代临床试验将使用对NK细胞CD16具有更高亲和力的mAb联合工程化NK细胞,有望为癌症患者提供更有效、质量更高的治疗。
Natural killer (NK) cells are cellular components of the innate immune system that can recognize and suppress the proliferation of cancer cells. NK cells can eliminate cancer cells through direct lysis, by secreting perforin and granzymes, or through antibody-dependent cell-mediated cytotoxicity (ADCC). ADCC involves the binding of the Fc gamma receptor IIIa (CD16), present on NK cells, to the constant region of an antibody already bound to cancer cells. Cancer cells use several mechanisms to evade antitumor activity of NK cells, including the accumulation of inhibitory cytokines, recruitment and expansion of immune suppressor cells such as myeloid-derived suppressor cells (MDSCs) and regulatory T cells (Tregs), modulation of ligands for NK cells receptors. Several strategies have been developed to enhance the antitumor activity of NK cells with the goal of overcoming cancer cells resistance to NK cells. The three main strategies to engineer and boost NK cells cytotoxicity include boosting NK cells with modulatory cytokines, adoptive NK cell therapy, and the employment of engineered NK cells to enhance antibody-based immunotherapy.
Although the first two strategies improved the efficacy of NK cell-based therapy, there are still some limitations, including immune-related adverse events, induction of immune-suppressive cells and further cancer resistance to NK cell killing. One strategy to overcome these issues is the combination of monoclonal antibodies (mAbs) that mediate ADCC and engineered NK cells with potentiated anti-cancer activity.
The advantage of using mAbs with ADCC activity is that they can activate NK cells, but also favor the accumulation of immune effector cells to the tumor microenvironment (TME). Several clinical trials reported that combining engineered NK cells with mAbs with ADCC activity can result in a superior clinical response compared to mAbs alone. Next generation of clinical trials, employing engineered NK cells with mAbs with higher affinity for CD16 expressed on NK cells, will provide more effective and higher-quality treatments to cancer patients.
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