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:Enhancing NK Cell Activity in Colorectal Cancer with an Fc-Optimized Antibody Targeting CD276 (B7-H3).
Enhancing NK Cell Activity in Colorectal Cancer with an Fc-Optimized Antibody Targeting CD276 (B7-H3).
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
Fc 优化的抗 CD276 抗体 8H8_SDIE 有效增强了 NK 细胞对 CD276 阳性结直肠癌细胞的反应性,并在体外诱导了肿瘤细胞裂解。
结直肠癌(CRC)因发病率和死亡率高,尤其在晚期治疗选择有限,是全球重要的健康负担。虽然阻断PD-1/PD-L1通路的疗法已显示临床获益,但其在CRC中的成功主要局限于微卫星高度不稳定(MSI-H)肿瘤患者。多数CRC病例亟需创新免疫治疗方案。CD276(B7-H3)是B7家族免疫检查点分子,在包括CRC在内的多种癌症中过表达。既往研究已显示,CRC细胞系中的CD276表达显著高于良性组织。本研究评估了Fc优化的抗CD276单克隆抗体增强CRC中自然杀伤(NK)细胞活性的潜力。
开发了Fc优化单克隆抗体8H8_SDIE,通过增强CD16结合来提高NK细胞活性。采用人CRC细胞系和健康成年供者的外周血单个核细胞(PBMC)进行体外实验,评估8H8_SDIE对CD276的结合特异性。通过检测活化标志物(CD69、CD25和CD107a)上调及细胞毒性介质(IFNγ、颗粒酶B和穿孔素)分泌,评估NK细胞活化;并通过细胞毒性实验测定NK细胞介导的肿瘤细胞裂解。
8H8_SDIE特异性结合CD276阳性CRC细胞,并显著增强NK细胞活化,包括提高活化标志物和细胞毒性介质水平。在细胞毒性实验中,8H8_SDIE显示出强效的NK细胞介导CRC细胞裂解作用。
Fc优化的抗CD276抗体8H8_SDIE有效增强了NK细胞对CD276阳性CRC细胞的反应,并在体外诱导肿瘤细胞裂解。这些结果提示,8H8_SDIE有望成为CRC的新型免疫治疗候选药物,尤其适用于微卫星稳定型疾病患者;仍需在后续高级别临床前研究及未来临床研究中进一步评估。 结直肠癌(CRC)是最常诊断的恶性肿瘤之一,也是全球癌症相关死亡的重要原因。许多晚期CRC患者对现有治疗反应不佳,只有少数患者能从现有免疫疗法中获益,因此迫切需要开发能够惠及更广泛患者群体的替代疗法。本研究聚焦于CD276蛋白,该蛋白常在包括结直肠癌细胞在内的癌细胞中大量表达。研究人员制备了一种靶向CD276的工程化抗体(免疫分子,可帮助机体识别并攻击威胁),命名为8H8_SDIE,并优化其刺激NK细胞(一类可清除肿瘤细胞的免疫细胞)的能力。研究在实验室中对结直肠癌细胞进行测试。该抗体成功结合癌细胞并强烈激活NK细胞;活化后的NK细胞释放细胞毒性分子,诱导癌细胞死亡。这些结果提示8H8_SDIE可能成为结直肠癌的一种有前景的新型免疫疗法。尽管在用于患者治疗前还需更多研究,本研究展示了一种有潜力改善这一棘手疾病治疗选择的方法。
An Fc-optimized monoclonal antibody, 8H8_SDIE, was developed to enhance NK cell activity by increasing CD16 binding. In vitro experiments were conducted using human CRC cell lines and peripheral blood mononuclear cells (PBMCs) from healthy adult donors to evaluate the binding specificity of 8H8_SDIE to CD276. NK cell activation was assessed by measuring the upregulation of activation markers (CD69, CD25, and CD107a) and secretion of cytotoxic mediators (IFN , granzyme B, and perforin). Cytotoxicity assays were performed to determine NK cell-mediated tumor cell lysis.
8H8_SDIE specifically bound to CD276-positive CRC cells and significantly enhanced NK cell activation. These effects included increased levels of activation and cytotoxic mediators. In cytotoxicity assays, 8H8_SDIE demonstrated potent NK cell-mediated lysis of CRC cells.
The Fc-optimized anti-CD276 antibody 8H8_SDIE effectively enhanced NK cell reactivity against CD276-positive CRC cells and induced tumor cell lysis in vitro. These findings suggest that 8H8_SDIE holds potential as a novel immunotherapeutic candidate for CRC, particularly for patients with microsatellite-stable disease, and warrants further evaluation in advanced preclinical and future clinical studies. Colorectal cancer (CRC) ranks among the most frequently diagnosed malignancies and remains a major contributor to cancer-related mortality on a global scale. Many patients with advanced CRC do not respond well to current treatments, and only a small number benefit from existing immunotherapies. This highlights the urgency of developing alternative treatments that could benefit a broader range of patients. In this study, we focused on a protein called CD276, which is often found in large amounts in cancer cells, including colorectal cancer cells. We created a specially engineered antibody (a type of immune molecule that helps the body recognize and attack threats) targeting CD276. This antibody, named 8H8_SDIE, was optimized to stimulate natural killer (NK) cells - a type of immune cell capable of eliminating tumor cells. We tested the antibody in the laboratory on colorectal cancer cells. The antibody successfully bound to cancer cells and strongly activated NK cells. After activation, NK cells released cytotoxic molecules which induced cancer cell death. These results suggest that 8H8_SDIE could be a promising new immunotherapy for colorectal cancer. Although more studies are needed before this can be used to treat patients, this study demonstrates a potential approach to improving treatment options for people with this challenging disease.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。