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免疫光动力疗法(IPDT):有机光敏剂及其在癌症消融中的应用

Immuno-photodynamic Therapy (IPDT): Organic Photosensitizers and Their Application in Cancer Ablation.

作者信息

Lu Yang, Sun Wen, Du Jianjun, Fan Jiangli, Peng Xiaojun

机构信息

State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials, Dalian University of Technology, Dalian 116024, P.R. China.

State Key Laboratory of Fine Chemicals, College of Materials Science and Engineering, Shenzhen University, Shenzhen 518071, P. R. China.

出版信息

JACS Au. 2023 Feb 14;3(3):682-699. doi: 10.1021/jacsau.2c00591. eCollection 2023 Mar 27.

Abstract

Photosensitizer-based photodynamic therapy (PDT) has been considered as a promising modality for fighting diverse types of cancers. PDT directly inhibits local tumors by a minimally invasive strategy, but it seems to be incapable of achieving complete eradication and fails to prevent metastasis and recurrence. Recently, increasing events proved that PDT was associated with immunotherapy by triggering immunogenic cell death (ICD). Upon a specific wavelength of light irradiation, the photosensitizers will turn the surrounding oxygen molecules into cytotoxic reactive oxygen species (ROS) for killing the cancer cells. Simultaneously, the dying tumor cells release tumor-associated antigens, which could improve immunogenicity to activate immune cells. However, the progressively enhanced immunity is typically limited by the intrinsic immunosuppressive tumor microenvironment (TME). To overcome this obstacle, immuno-photodynamic therapy (IPDT) has come to be one of the most beneficial strategies, which takes advantage of PDT to stimulate the immune response and unite immunotherapy for inducing immune-OFF tumors to immune-ON ones, to achieve systemic immune response and prevent cancer recurrence. In this Perspective, we provide a review of recent advances in organic photosensitizer-based IPDT. The general process of immune responses triggered by photosensitizers (PSs) and how to enhance the antitumor immune pathway by modifying the chemical structure or conjugating with a targeting component was discussed. In addition, future perspectives and challenges associated with IPDT strategies are also discussed. We hope this Perspective could inspire more innovative ideas and provide executable strategies for future developments in the war against cancer.

摘要

基于光敏剂的光动力疗法(PDT)被认为是一种对抗多种癌症的有前景的方法。PDT通过微创策略直接抑制局部肿瘤,但似乎无法实现完全根除,也无法预防转移和复发。最近,越来越多的事件证明PDT通过触发免疫原性细胞死亡(ICD)与免疫疗法相关联。在特定波长的光照射下,光敏剂会将周围的氧分子转化为细胞毒性活性氧(ROS)以杀死癌细胞。同时,垂死的肿瘤细胞释放肿瘤相关抗原,这可以提高免疫原性以激活免疫细胞。然而,逐渐增强的免疫力通常受到肿瘤内在免疫抑制微环境(TME)的限制。为了克服这一障碍,免疫光动力疗法(IPDT)已成为最有益的策略之一,它利用PDT刺激免疫反应并联合免疫疗法,将免疫关闭的肿瘤转变为免疫开启的肿瘤,以实现全身免疫反应并预防癌症复发。在这篇观点文章中,我们综述了基于有机光敏剂的IPDT的最新进展。讨论了光敏剂(PSs)触发免疫反应的一般过程,以及如何通过修饰化学结构或与靶向成分结合来增强抗肿瘤免疫途径。此外,还讨论了与IPDT策略相关的未来前景和挑战。我们希望这篇观点文章能够激发更多创新想法,并为未来抗癌战争的发展提供可执行的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c744/10052235/7533bcc0b917/au2c00591_0001.jpg

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