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:Development of a novel (18)F-labeled radiotracer targeting granzyme B for imaging early tumor responses to immunotherapy.
Development of a novel (18)F-labeled radiotracer targeting granzyme B for imaging early tumor responses to immunotherapy.
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18 F-G1 是一种有效的颗粒酶 B 成像放射性示踪剂。其优越的成像特性使其成为一种有前景的工具,可用于以高灵敏度无创评估各种类型免疫疗法的疗效。
免疫治疗已成为恶性肿瘤治疗的一个有前景的途径,但在体内验证其抗肿瘤活性的方法仍然有限。颗粒酶B是免疫介导细胞死亡的关键介质,是评估免疫治疗疗效的潜在生物标志物。本研究旨在开发一种高灵敏度和高特异性的放射性示踪剂,用于颗粒酶B的体内成像。
合成了10种granzyme B靶向抑制剂并评估其结合亲和力。最有前景的化合物与1,4,7-三氮杂环壬烷-N,N',N"-三乙酸螯合剂偶联,并用Al 18 F放射性标记生成放射性示踪剂18 F-G1。将其成像和药代动力学特性与最近开发的放射性示踪剂68 Ga-grazytracer进行了比较。18 F-G1被用于评估T细胞介导和自然杀伤(NK)细胞介导的抗肿瘤免疫。此外,还使用18 F-G1对环鸟苷酸-腺苷酸合成酶-干扰素基因刺激因子(cGAS-STING)通路靶向治疗进行了定量评估。
18 F-G1通过简单的放射性标记程序制备,放射化学纯度高达>98%。与grazytracer相比,其颗粒酶B结合亲和力提高了4.2倍。在抗程序性细胞死亡蛋白-1抗体治疗的MC38肿瘤模型中,18 F-G1优于68 Ga-grazytracer,具有显著更高的肿瘤摄取(最大肿瘤摄取增加2.1倍)和更优的肿瘤与肌肉对比度(7.46 vs 2.33)。对于基于NK细胞的治疗,18 F-G1正电子发射断层扫描(PET)/CT成功监测了NK-92MI细胞注射后颗粒酶B的释放,注射后24小时观察到峰值信号。与其他cGAS-STING通路靶向药物治疗相比,18 F-G1 PET/CT检测到SR-717治疗的肿瘤中强烈的免疫激活,这与最高的CD8 + T细胞浸润、颗粒酶B表达水平和肿瘤生长抑制相关。
Immunotherapy has emerged as a promising avenue for malignant tumors treatment, but methods to validate its in vivo antitumor activity remain limited. Granzyme B, a key mediator of immune-mediated cell death, is a potential biomarker for assessing immunotherapy efficacy. This study aimed to develop a radiotracer with high sensitivity and specificity for in vivo imaging of granzyme B.
10 granzyme B targeting inhibitors were synthesized and evaluated to improve binding affinity. The most promising compound was conjugated with 1,4,7-triazacyclononane-N,N',N"-triacetic acid chelator and radiolabeled with Al 18 F to generate radiotracer 18 F-G1. Its imaging and pharmacokinetic properties were compared with those of the recently developed radiotracer 68 Ga-grazytracer. 18 F-G1 was applied to assess T cell-mediated and natural killer (NK) cell-mediated antitumor immunity. In addition, the cyclic guanosine monophosphate AMP synthase-stimulator of interferon genes (cGAS-STING) pathway-targeted therapies were also quantitatively evaluated using 18 F-G1.
18 F-G1 was produced with high radiochemical purity of >98% through a simple radiolabeling procedure. It displayed a 4.2-fold improvement in granzyme B binding affinity compared with grazytracer. In the anti-programmed cell death protein-1 antibody-treated MC38 tumor model, 18 F-G1 outperformed 68 Ga-grazytracer with significantly higher tumor uptake (2.1-fold increase in maximum tumor uptake) and superior tumor-to-muscle contrast (7.46 vs 2.33). For NK cell-based therapy, 18 F-G1 positron emission tomography (PET)/CT successfully monitored granzyme B release following NK-92MI cell injection, with peak signals observed 24 hours postinjection. 18 F-G1 PET/CT detected robust immune activation in SR-717-treated tumors compared with other cGAS-STING pathway-targeted drug treatments, which correlated with the highest CD8 + T cell infiltration, granzyme B expression level and tumor growth inhibition.
18 F-G1 is an effective granzyme B imaging radiotracer. Its superior imaging properties make it a promising tool for non-invasively evaluating the therapeutic efficacy of various types of immunotherapies with high sensitivity.
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