通过靶向肿瘤相关巨噬细胞的嵌合受体工程化溶瘤病毒重振内源性抗肿瘤免疫
Rejuvenating endogenous antitumor immunity via a chimeric receptor-engineered oncolytic virus targeting tumor-associated macrophages.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Current trends on immunotherapy for oncology.
Current trends on immunotherapy for oncology.
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免疫治疗利用患者自身免疫系统识别并清除肿瘤细胞,彻底改变了肿瘤学,并使多种恶性肿瘤获得持久应答。过去十年,靶向CTLA-4、PD-1和PD-L1的免疫检查点抑制剂已成为多种实体瘤的标准治疗,而嵌合抗原受体(CAR)T细胞疗法治疗血液系统恶性肿瘤也显示出显著疗效。尽管取得这些成功,原发性和获得性耐药、免疫相关毒性及治疗成本高等挑战仍限制其更广泛应用。新兴策略包括靶向LAG-3、TIGIT等新型检查点、开发新一代细胞疗法、癌症疫苗和溶瘤病毒,目前均在积极研究,以扩大治疗选择并改善患者结局。开发用于患者筛选的生物标志物,以及将免疫疗法与化疗、靶向药物和放疗联合,对于克服耐药机制至关重要。展望未来,利用肿瘤新抗原和肿瘤微环境的个体化免疫治疗方法,有望带来更精准有效的治疗。
Immunotherapy has revolutionized oncology by harnessing the patient's own immune system to recognize and eliminate tumor cells, leading to durable responses in a variety of malignancies. Over the past decade, immune checkpoint inhibitors targeting CTLA-4, PD-1, and PD-L1 have become standard of care across multiple solid tumors, while chimeric antigen receptor (CAR) T-cell therapies have demonstrated remarkable efficacy in hematologic cancers. Despite these successes, challenges such as primary and acquired resistance, immune-related toxicities, and high treatment costs continue to limit broader application.
Emerging strategies including novel checkpoint targets ( e. g. , LAG-3, TIGIT), next-generation cellular therapies, cancer vaccines, and oncolytic viruses are under active investigation to expand therapeutic options and improve patient outcomes.
Biomarker development for patient selection and combination regimens with chemotherapy, targeted agents, and radiation are critical to overcoming resistance mechanisms. Looking ahead, personalized immunotherapy approaches leveraging tumor neoantigens and the tumor microenvironment hold promise for more precise and effective treatments.
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 →
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