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基于纳米材料的药物传递系统:癌症免疫治疗的新武器。

Nanomaterial-Based Drug Delivery Systems: A New Weapon for Cancer Immunotherapy.

机构信息

Clinical Medical College, Yangzhou University, Yangzhou, 225000, People's Republic of China.

Department of General Surgery, Institute of General Surgery, Northern Jiangsu Province Hospital, Clinical Medical College, Yangzhou University, Yangzhou, 225000, People's Republic of China.

出版信息

Int J Nanomedicine. 2022 Oct 3;17:4677-4696. doi: 10.2147/IJN.S376216. eCollection 2022.


DOI:10.2147/IJN.S376216
PMID:36211025
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9541303/
Abstract

Cancer immunotherapy, a major breakthrough in cancer treatment, has been successfully applied to treat a number of tumors. However, given the presence of factors in the tumor microenvironment (TME) that impede immunotherapy, only a small proportion of patients achieve a good clinical response. With the ability to increase permeability and cross biological barriers, nanomaterials have been successfully applied to deliver immunotherapeutic agents, thus realizing the anti-cancer therapeutic potential of therapeutic agents. This has driven a wave of research into systems for the delivery of immunotherapeutic agents, which has resulted in widespread interest in nanomaterial-based drug delivery systems. Nanomaterial-based drug delivery systems are able to overcome the challenges from TME and thus achieve good results in cancer immunotherapy. If it can make a breakthrough in improving biocompatibility and reducing cytotoxicity, it will be more widely used in clinical practice. Different types of nanomaterials may also have some subtle differences in enhancing cancer immunotherapy. Moreover, delivery systems made of nanomaterials loaded with drugs, such as cytotoxic drugs, cytokines, and adjuvants, could be used for cancer immunotherapy because they avoid the toxicity and side effects associated with these drugs, thereby enabling their reuse. Therefore, further insights into nanomaterial-based drug delivery systems will provide more effective treatment options for cancer patients.

摘要

癌症免疫疗法是癌症治疗的重大突破,已成功应用于治疗多种肿瘤。然而,鉴于肿瘤微环境(TME)中存在阻碍免疫疗法的因素,只有一小部分患者能获得良好的临床反应。纳米材料具有增加通透性和跨越生物屏障的能力,已成功应用于传递免疫治疗剂,从而实现治疗剂的抗癌治疗潜力。这推动了免疫治疗剂传递系统的研究热潮,因此纳米材料为基础的药物传递系统引起了广泛关注。纳米材料为基础的药物传递系统能够克服 TME 的挑战,从而在癌症免疫疗法中取得良好的效果。如果能够在提高生物相容性和降低细胞毒性方面取得突破,将更广泛地应用于临床实践。不同类型的纳米材料在增强癌症免疫疗法方面也可能存在一些细微差异。此外,载药纳米材料(如细胞毒性药物、细胞因子和佐剂)的递送系统可用于癌症免疫治疗,因为它们避免了这些药物相关的毒性和副作用,从而可以重复使用。因此,进一步深入研究纳米材料为基础的药物传递系统将为癌症患者提供更有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4aa/9541303/8a977d06ef64/IJN-17-4677-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4aa/9541303/96e59bcb28df/IJN-17-4677-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4aa/9541303/688dad863e38/IJN-17-4677-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4aa/9541303/8a977d06ef64/IJN-17-4677-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4aa/9541303/96e59bcb28df/IJN-17-4677-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4aa/9541303/688dad863e38/IJN-17-4677-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4aa/9541303/8a977d06ef64/IJN-17-4677-g0003.jpg

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Nanomaterial-Based Drug Delivery Systems: A New Weapon for Cancer Immunotherapy.

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[5]
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[6]
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本文引用的文献

[1]
Advances in endocrine toxicity of nanomaterials and mechanism in hormone secretion disorders.

J Appl Toxicol. 2022-7

[2]
Tumor-Microenvironment-Responsive Nanomedicine for Enhanced Cancer Immunotherapy.

Adv Sci (Weinh). 2022-1

[3]
Nanotechnology-based products for cancer immunotherapy.

Mol Biol Rep. 2022-2

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Crosstalk between cancer-associated fibroblasts and immune cells in the tumor microenvironment: new findings and future perspectives.

Mol Cancer. 2021-10-11

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Recent Adv Drug Deliv Formul. 2021

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Recent Progress in Lipid Nanoparticles for Cancer Theranostics: Opportunity and Challenges.

Pharmaceutics. 2021-6-7

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J Adv Res. 2021-7

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J Hematol Oncol. 2021-5-31

[9]
Recent Advances in Preclinical Research Using PAMAM Dendrimers for Cancer Gene Therapy.

Int J Mol Sci. 2021-3-13

[10]
Antibody-drug nanoparticle induces synergistic treatment efficacies in HER2 positive breast cancer cells.

Sci Rep. 2021-4-1

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