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:The development of a next generation NK cell engager platform by integrating a potency-reduced IL-15 variant to enhance antitumor activity.
The development of a next generation NK cell engager platform by integrating a potency-reduced IL-15 variant to enhance antitumor activity.
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通过将 IL15v 整合到我们基于 anti-NKp46 的 NKCE 中,IL15v-NKCE 表现出增强的抗肿瘤疗效,同时保持可接受的安全性,从而使其成为 NK 细胞治疗中有前景的下一代治疗模式。
NK 细胞接合抗体(NKCE)近期受到关注。传统NKCE虽安全性尚可,但抗肿瘤疗效较温和,因此需要开发新一代NKCE以提高疗效。IL-15是NK细胞的重要激活因子,已被探索用于NKCE设计;然而,野生型IL-15在临床试验中显示显著毒性。本研究在专有抗NKp46型NKCE中加入效力减弱的IL-15变体(IL15v),开发新型四价NKCE平台IL15v-NKCE。
通过检测原代免疫细胞中的pSTAT5诱导水平和IL-15报告细胞系中的STAT5激活情况,评估IL15v组分活性。利用NK细胞与肿瘤细胞共培养评估IL15v-NKCE体外活性,并在荷瘤小鼠模型中评价其体内抗肿瘤疗效和安全性。
体外实验显示,IL15v可选择性激活NK细胞而不影响T细胞,增强NKCE细胞毒性,抑制NK细胞凋亡并促进其增殖。体内实验中,IL15v-NKCE耐受性良好,且抗肿瘤疗效优于传统NKCE。IL15v-NKCE的四个组分(抗NKp46、Fc、IL15v和抗肿瘤相关抗原)对于达到最大活性均不可或缺。在临床前模型中,IL15v-NKCE与抗PD-1联合的效力也高于传统NKCE。
将IL15v整合至抗NKp46型NKCE后,IL15v-NKCE在保持可接受安全性的同时提高了抗肿瘤疗效,因此有望成为新一代NK细胞治疗方式。
Natural killer cell engager (NKCE) has gained attention recently. Conventional NKCEs exhibit mild anti-tumor efficacy despite acceptable safety profiles. Therefore, next-generation NKCE development is essential to enhance efficacy. IL-15, a key NK cell activator, is explored in NKCE design. However, wild-type IL-15 shows significant toxicity in clinical trials. In this study, we present the development of a novel tetravalent NKCE platform (IL15v-NKCE) by incorporating a potency-reduced IL-15 element (IL15v) into our proprietary anti-NKp46 based NKCEs.
The activity of the IL15v moiety was assessed by quantifying pSTAT5 induction in primary immune cells and evaluating STAT5 activation in an IL-15 reporter cell line. The in vitro activity of IL15v-NKCE was determined using co-culture assays with NK and tumor cells. The in vivo anti-tumor efficacy and safety profile of IL15v-NKCE were evaluated in tumor-bearing mouse models.
In vitro , IL15v selectively activates NK cells without affecting T cells, enhances NKCE cytotoxicity, prevents NK apoptosis, and promotes NK proliferation. In vivo , IL15v-NKCE shows good tolerability and superior anti-tumor efficacy compared to conventional NKCE. All four components (anti-NKp46, Fc, IL15v, anti-tumor-associated antigen) of IL15v-NKCE are essential for maximal activity, and IL15v-NKCE is more potent than the conventional NKCE when combined with anti-PD-1 in preclinical models.
By integrating IL15v into our anti-NKp46 based NKCEs, IL15v-NKCE has exhibited enhanced anti-tumor efficacy while maintaining an acceptable safety profile, thereby positioning it as a promising next-generation therapeutic modality for NK cell-based therapy.
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