← 返回前沿论文

智能多组学与工业 6.0 和 7.0 赋能技术:解析肿瘤免疫微环境并推进癌症免疫治疗

英文原题:Intelligent multi omics and industry 6.0 and 7.0 enabled technologies for deciphering the tumor immune microenvironment and advancing cancer immunotherapy.

查看英文原题

Intelligent multi omics and industry 6.0 and 7.0 enabled technologies for deciphering the tumor immune microenvironment and advancing cancer immunotherapy.

PubMed 2026/01/31(内容时间) Toxicol Res (Camb) Q3 · IF 2.9(JCR 2025)

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。

研究概要

癌症免疫治疗的最新进展已彻底改变了临床肿瘤学领域,单克隆抗体(mAbs)、免疫检查点抑制剂、过继性细胞疗法、溶瘤病毒、基于细胞因子的治疗药物以及纳米医学已成为核心治疗平台。

中文摘要

癌症免疫治疗近期进展改变了临床肿瘤学格局,单克隆抗体(mAb)、免疫检查点抑制剂、过继细胞疗法、溶瘤病毒、细胞因子疗法和纳米医学已成为核心治疗平台。肿瘤间及瘤内基因组差异造成的肿瘤异质性会形成复杂新抗原谱,促成免疫逃逸和治疗耐药。槲皮素、姜黄素、儿茶素和白藜芦醇等天然抗氧化剂因能够调节免疫代谢通路而日益受到重视:它们可降低病理性活性氧(ROS)、恢复T细胞受体信号、增强树突状细胞抗原呈递并改善CD8⁺ T细胞浸润,从而强化基础抗肿瘤免疫应答。由单个B细胞克隆产生的单克隆抗体具有较高抗原特异性,可通过抗体依赖性细胞介导细胞毒作用、补体活化和免疫检查点调节发挥抗肿瘤作用。尽管检查点抑制剂临床疗效显著,但也可能诱发严重免疫相关不良事件,包括心肌炎、结肠炎和肺炎。机制研究还显示,EGCG、α-硫辛酸和姜黄素等抗氧化剂可通过恢复线粒体功能并抑制STAT3信号,下调PD-1/PD-L1表达,最终增强T细胞活化、减少耗竭并提高对检查点阻断的应答。CAR-T 和CAR-NK等过继细胞平台可产生持久临床应答,但仍面临细胞因子释放综合征、抗原逃逸和神经毒性等挑战。人工智能驱动的多组学分析现已具备预测能力,可用于精准诊断、生物标志物发现和优化治疗规划。整合工业6.0/7.0技术、智能制造、可持续材料、低碳生物工艺和自主系统,将有助于开发全球可及、靶向性强且毒性较低的免疫疗法,支持新一代癌症治疗实现公平且环境负责的应用。

展开英文摘要原文

Recent advancements in cancer immunotherapy have transformed clinical oncology, with monoclonal antibodies (mAbs), immune checkpoint inhibitors, adoptive cellular therapies, oncolytic viruses, cytokine based therapeutics and nanomedicine establishing themselves as core treatment platforms. Tumor heterogeneity driven by inter and intra tumoral genomic divergence generates complex neoantigen landscapes, contributing to immune evasion and therapeutic resistance. Natural antioxidants such as quercetin, curcumin, catechins and resveratrol are gaining recognition for their ability to modulate immunometabolic pathways by lowering pathological reactive oxygen species (ROS), restoring T-cell receptor signaling, enhancing dendritic antigen presentation and improving CD8 + T-cell infiltration, thereby strengthening foundational antitumor immune responses. Monoclonal antibodies generated from single B-cell clones demonstrate high antigen specificity and exert antitumor effects through antibody-dependent cellular cytotoxicity, complement activation and immune checkpoint modulation. Although checkpoint inhibitors achieve substantial clinical efficacy, they may induce severe immune-related adverse events, including myocarditis, colitis, and pneumonitis. Mechanistic studies further reveal that antioxidants such as EGCG, -lipoic acid and curcumin downregulate PD-1/PD-L1 expression by restoring mitochondrial function and inhibiting STAT3 signalling, ultimately enhancing T-cell activation and reducing exhaustion, thereby improving responsiveness to checkpoint blockade. Adoptive cellular platforms, including CAR-T and CAR-NK therapies, offer durable clinical responses but face challenges such as cytokine release syndrome, antigen escape and neurotoxicity. AI-driven multi-omics analytics now achieve predictive accuracies enabling precision diagnostics, biomarker discovery and optimized treatment planning. Integrating Industry 6.0/7.0 technologies, intelligent manufacturing, sustainable materials, low-carbon bioprocessing, autonomous systems will facilitate globally accessible, highly targeted and toxicity-reduced immunotherapies, supporting equitable and environmentally responsible implementation of next-generation cancer treatments.

论文信息

作者
Majeed H、Irfan M、Irfan M、Iftikhar T
第一作者单位
Department of Chemistry, University of Management and Technology (UMT), Lahore, Sialkot Sub Campus, Sialkot 51310, Pakistan.
通讯作者单位
Department of Botany, Government College University Lahore, 54000, Pakistan.
文献类型
综述
期刊
Toxicology research2026 Feb
原文标识
PubMed 41623584 · DOI 10.1093/toxres/tfag002