Azmal Mahir, Miah Md Munna, Prima Fatema Sultana, Paul Jibon Kumar, Haque Anm Shah Newaz Been, Ghosh Ajit
Department of Biochemistry and Molecular Biology, Shahjalal University of Science and Technology, Sylhet, Bangladesh.
Department of Biochemistry and Molecular Biology, Shahjalal University of Science and Technology, Sylhet, Bangladesh.
Semin Oncol. 2025 Apr 29;52(3):152345. doi: 10.1016/j.seminoncol.2025.152345.
Cancer immunotherapy has transformed oncology by harnessing the immune system to specifically target cancer cells, offering reduced systemic toxicity compared to traditional therapies. This review highlights key strategies, including adoptive cell transfer (ACT), immune checkpoint inhibitors, oncolytic viral (OV) therapy, monoclonal antibodies (mAbs), and mRNA-based vaccines. ACT reinfuses enhanced immune cells like tumor-infiltrating lymphocytes (TILs) to combat refractory cancers, while checkpoint inhibitors (eg, PD-1 and CTLA-4 blockers) restore T-cell activity. OV therapy uses engineered viruses (eg, T-VEC) to selectively lyse cancer cells, and advanced mAbs improve targeting precision. mRNA vaccines introduce tumor-specific antigens to trigger robust immune responses. Despite significant progress, challenges like immune-related side effects, high costs, and immunosuppressive tumor microenvironments persist. This review underscores the need for combination strategies and precision medicine to overcome these barriers and maximize the potential of immunotherapy in personalized cancer treatment.
癌症免疫疗法通过利用免疫系统特异性靶向癌细胞,彻底改变了肿瘤学,与传统疗法相比,其全身毒性更低。本综述重点介绍了关键策略,包括过继性细胞转移(ACT)、免疫检查点抑制剂、溶瘤病毒(OV)疗法、单克隆抗体(mAb)和基于mRNA的疫苗。ACT重新注入增强的免疫细胞,如肿瘤浸润淋巴细胞(TIL),以对抗难治性癌症,而检查点抑制剂(如PD-1和CTLA-4阻滞剂)可恢复T细胞活性。OV疗法使用工程病毒(如T-VEC)选择性地裂解癌细胞,先进的单克隆抗体提高了靶向精度。mRNA疫苗引入肿瘤特异性抗原以触发强烈的免疫反应。尽管取得了重大进展,但免疫相关副作用、高成本和免疫抑制性肿瘤微环境等挑战依然存在。本综述强调了采用联合策略和精准医学来克服这些障碍,并在个性化癌症治疗中最大限度发挥免疫疗法潜力(的必要性)。
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