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:ATOR-1017 (evunzekibart), an Fc-gamma receptor conditional 4-1BB agonist designed for optimal safety and efficacy, activates exhausted T cells in combination with anti-PD-1.
ATOR-1017 (evunzekibart), an Fc-gamma receptor conditional 4-1BB agonist designed for optimal safety and efficacy, activates exhausted T cells in combination with anti-PD-1.
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这些临床前数据表明 ATOR-1017 具有良好的安全性特征,以及作为单一疗法和与抗 PD1 联合使用的强效治疗作用,支持 ATOR-1017 的进一步临床开发。
4-1BB (CD137) 是一种共刺激受体,高表达于肿瘤反应性效应 T 细胞和 NK 细胞,受到刺激后可延长肿瘤反应性效应 T 细胞和 NK 细胞在肿瘤内的持久性,并诱导长寿命记忆 T 细胞。4-1BB 激动性抗体已被证明可诱导强大的抗肿瘤效应,并与免疫检查点抑制剂产生协同作用。然而,第一代 4-1BB 激动剂受到剂量限制性毒性的阻碍,导致剂量水平不理想或激动活性不佳。
ATOR-1017(evunzekibart)是一种第二代 Fc-gamma 受体条件性 4-1BB 激动剂,采用 IgG4 格式,旨在克服第一代 4-1BB 激动剂的局限性,在提供强效激动作用的同时,最大限度减少全身性免疫激活和肝毒性风险。通过 X 射线晶体学确定了 ATOR-1017 的表位,并在体外和体内评估了其作为单药治疗或与 anti-PD1 联合治疗的功能活性。
ATOR-1017与4-1BB上的独特表位结合,使ATOR-1017能够以交联依赖、FcγR条件性的方式激活T细胞,包括具有耗竭表型的细胞,以及NK细胞。这在体内转化为针对肿瘤的强效抗肿瘤治疗效果,并且与抗PD-1治疗联合时效果进一步增强。
4-1BB (CD137) is a co-stimulatory receptor highly expressed on tumor reactive effector T cells and NK cells, which upon stimulation prolongs persistence of tumor reactive effector T and NK cells within the tumor and induces long-lived memory T cells. 4-1BB agonistic antibodies have been shown to induce strong anti-tumor effects that synergize with immune checkpoint inhibitors. The first generation of 4-1BB agonists was, however, hampered by dose-limiting toxicities resulting in suboptimal dose levels or poor agonistic activity.
ATOR-1017 (evunzekibart), a second-generation Fc-gamma receptor conditional 4-1BB agonist in IgG4 format, was designed to overcome the limitations of the first generation of 4-1BB agonists, providing strong agonistic effect while minimizing systemic immune activation and risk of hepatoxicity. The epitope of ATOR-1017 was determined by X-ray crystallography, and the functional activity was assessed in vitro and in vivo as monotherapy or in combination with anti-PD1.
ATOR-1017 binds to a unique epitope on 4-1BB enabling ATOR-1017 to activate T cells, including cells with an exhausted phenotype, and NK cells, in a cross-linking dependent, FcγR-conditional, manner. This translated into a tumor-directed and potent anti-tumor therapeutic effect in vivo, which was further enhanced with anti-PD-1 treatment.
These preclinical data demonstrate a strong safety profile of ATOR-1017, together with its potent therapeutic effect as monotherapy and in combination with anti-PD1, supporting further clinical development of ATOR-1017.
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