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靶向程序性死亡配体1(PD-L1)的免疫微泡复合物提高小鼠结肠癌模型的治疗指数

PD-L1 Targeting Immune-Microbubble Complex Enhances Therapeutic Index in Murine Colon Cancer Models.

作者信息

Kim Daehyun, Lee Seung Soo, Moon Hyungwon, Park So Yeon, Lee Hak Jong

机构信息

Department of Nano Science and Technology, Graduate School of Convergence Science and Technology, Seoul National University, Seoul 08826, Korea.

Department of Radiology, Seoul National University Bundang Hospital, 82 Gumi-ro 173, Bundang-gu, Seongnam 13620, Korea.

出版信息

Pharmaceuticals (Basel). 2020 Dec 23;14(1):6. doi: 10.3390/ph14010006.

DOI:10.3390/ph14010006
PMID:33374574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7822446/
Abstract

Cancer immunotherapy has revolutionized the way different neoplasms are treated. Among the different variations of cancer immunotherapy, the checkpoint inhibitors targeting the programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) axis have been validated and are currently used in the clinics. Nevertheless, these therapeutic antibodies are associated with significant side effects and are known to induce immune-related toxicities. To address these issues, we have developed an immune-microbubble complex (IMC) which not only reduces the toxicities associated with the antibodies but also enhances the therapeutic efficacy when combined with focused ultrasound. The concept of IMCs could be applied to any type of antibody-based treatment regimens to maximize their therapeutic potential.

摘要

癌症免疫疗法彻底改变了不同肿瘤的治疗方式。在癌症免疫疗法的不同变体中,靶向程序性细胞死亡蛋白1(PD-1)/程序性死亡配体1(PD-L1)轴的检查点抑制剂已得到验证,目前正在临床中使用。然而,这些治疗性抗体与显著的副作用相关,并且已知会诱导免疫相关毒性。为了解决这些问题,我们开发了一种免疫微泡复合物(IMC),它不仅降低了与抗体相关的毒性,而且在与聚焦超声联合使用时还提高了治疗效果。IMC的概念可应用于任何基于抗体的治疗方案,以最大限度地发挥其治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c97/7822446/6d3e51acb28b/pharmaceuticals-14-00006-g007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c97/7822446/c12c65a8e837/pharmaceuticals-14-00006-g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c97/7822446/5ea83f728769/pharmaceuticals-14-00006-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c97/7822446/0a6d1f195166/pharmaceuticals-14-00006-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c97/7822446/098d1674e365/pharmaceuticals-14-00006-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c97/7822446/e0b67fb50979/pharmaceuticals-14-00006-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c97/7822446/c12c65a8e837/pharmaceuticals-14-00006-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c97/7822446/774b75f27c20/pharmaceuticals-14-00006-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c97/7822446/6d3e51acb28b/pharmaceuticals-14-00006-g007.jpg

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Combination Therapy with Doxorubicin-Loaded Reduced Albumin Nanoparticles and Focused Ultrasound in Mouse Breast Cancer Xenografts.阿霉素负载的还原型白蛋白纳米颗粒与聚焦超声联合治疗小鼠乳腺癌异种移植瘤
Pharmaceuticals (Basel). 2020 Sep 7;13(9):235. doi: 10.3390/ph13090235.
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Immunomodulation of intracranial melanoma in response to blood-tumor barrier opening with focused ultrasound.
递送靶向癌症中PD-1/PD-L1免疫检查点的免疫疗法的替代策略
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Cavitation-Mediated Immunomodulation and Its Use with Checkpoint Inhibitors.空化介导的免疫调节及其与检查点抑制剂的联合应用。
Pharmaceutics. 2023 Aug 9;15(8):2110. doi: 10.3390/pharmaceutics15082110.
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Co-Delivery Nanomicelles for Potentiating TNBC Immunotherapy by Synergetically Reshaping CAFs-Mediated Tumor Stroma and Reprogramming Immunosuppressive Microenvironment.共递纳米胶束通过协同重塑 CAFs 介导的肿瘤基质和重新编程免疫抑制微环境来增强三阴性乳腺癌免疫治疗。
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