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巨噬细胞作为抗癌治疗中纳米颗粒递呈的有前途载体。

Macrophages as Promising Carriers for Nanoparticle Delivery in Anticancer Therapy.

机构信息

Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.

出版信息

Int J Nanomedicine. 2023 Aug 8;18:4521-4539. doi: 10.2147/IJN.S421173. eCollection 2023.

Abstract

Macrophages play a critical role in the immune response due to their ability to recognize and remove pathogens, as well as present antigens, which are involved in inflammation, but they are also one of the most abundant immune cell populations present in the tumor microenvironment. In recent years, macrophages have become promising cellular carriers for drug and nanoparticle delivery to the tumor microenvironment, mainly due to their natural properties such as biocompatibility, degradability, lack of immunogenicity, long half-life in circulation, crossing biological barriers, and the possibility of migration and accumulation at a site of inflammation such as a tumor. For the effectiveness of this therapeutic strategy, known as "Trojan horse", it is important that the nanoparticles engulfed by macrophages do not affect their proper functioning. In our review, we discussed how the size, shape, chemical and mechanical properties of nanoparticles influence their internalization by macrophages. In addition, we described the promising research utilizing macrophages, their cell membranes and macrophage-derived exosomes as drug carriers in anticancer therapy. As a prospect of the wider use of this therapeutic strategy, we postulate its future application in boron delivery to the tumor environment in boron neutron capture therapy.

摘要

巨噬细胞在免疫反应中发挥着关键作用,因为它们能够识别和清除病原体,并呈递抗原,这些过程涉及炎症,但它们也是肿瘤微环境中最丰富的免疫细胞群体之一。近年来,巨噬细胞已成为药物和纳米颗粒递送至肿瘤微环境的有前途的细胞载体,主要是因为它们具有天然特性,如生物相容性、可降解性、缺乏免疫原性、在循环中的半衰期长、能够穿越生物屏障,并且有可能迁移和积聚在炎症部位,如肿瘤。为了使这种治疗策略(称为“特洛伊木马”)有效,被巨噬细胞吞噬的纳米颗粒不影响其正常功能非常重要。在我们的综述中,我们讨论了纳米颗粒的大小、形状、化学和机械性质如何影响它们被巨噬细胞内化。此外,我们还描述了利用巨噬细胞、其细胞膜和巨噬细胞衍生的外泌体作为抗癌治疗药物载体的有前途的研究。作为这种治疗策略更广泛应用的前景,我们假设其未来在硼中子俘获治疗中向肿瘤环境递送硼的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79b4/10422973/cc5ddf3888b1/IJN-18-4521-g0001.jpg

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