Nanomaterials in modulating tumor-associated macrophages and enhancing immunotherapy

重编程 免疫疗法 纳米材料 炎症 巨噬细胞 纳米技术 癌症研究 医学 免疫系统 免疫学 材料科学 化学 细胞 生物化学 体外
作者
Chen Liang,Yihan Zhang,Siyao Wang,Wangbo Jiao,Jingyi Guo,Nan Zhang,Xiaoli Liu
出处
期刊:Journal of Materials Chemistry B [Royal Society of Chemistry]
卷期号:12 (20): 4809-4823 被引量:9
标识
DOI:10.1039/d4tb00230j
摘要

Tumor-associated macrophages (TAMs) are predominantly present in the tumor microenvironment (TME) and play a crucial role in shaping the efficacy of tumor immunotherapy. These TAMs primarily exhibit a tumor-promoting M2-like phenotype, which is associated with the suppression of immune responses and facilitation of tumor progression. Interestingly, recent research has highlighted the potential of repolarizing TAMs from an M2 to a pro-inflammatory M1 status-a shift that has shown promise in impeding tumor growth and enhancing immune responsiveness. This concept is particularly intriguing as it offers a new dimension to cancer therapy by targeting the tumor microenvironment, which is a significant departure from traditional approaches that focus solely on tumor cells. However, the clinical application of TAM-modulating agents is often challenged by issues such as insufficient tumor accumulation and off-target effects, limiting their effectiveness and safety. In this regard, nanomaterials have emerged as a novel solution. They serve a dual role: as delivery vehicles that can enhance the accumulation of therapeutic agents in the tumor site and as TAM-modulators. This dual functionality of nanomaterials is a significant advancement as it addresses the key limitations of current TAM-modulating strategies and opens up new avenues for more efficient and targeted therapies. This review provides a comprehensive overview of the latest mechanisms and strategies involving nanomaterials in modulating macrophage polarization within the TME. It delves into the intricate interactions between nanomaterials and macrophages, elucidating how these interactions can be exploited to drive macrophage polarization towards a phenotype that is more conducive to anti-tumor immunity. Additionally, the review explores the burgeoning field of TAM-associated nanomedicines in combination with tumor immunotherapy. This combination approach is particularly promising as it leverages the strengths of both nanomedicine and immunotherapy, potentially leading to synergistic effects in combating cancer.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刻苦的天磊完成签到 ,获得积分10
刚刚
2秒前
弱有所思完成签到 ,获得积分10
2秒前
cyf完成签到,获得积分10
2秒前
2021完成签到 ,获得积分0
3秒前
青海姜超发布了新的文献求助10
4秒前
5秒前
6秒前
重要的黎昕完成签到,获得积分10
6秒前
酷波er的应助被野性的若烟采纳,获得10
6秒前
柒夏发布了新的文献求助20
6秒前
silence完成签到,获得积分10
7秒前
李健的小迷弟的应助被zh采纳,获得10
7秒前
7秒前
WZMZARD发布了新的文献求助10
9秒前
论高等数学的无用性完成签到 ,获得积分10
10秒前
Ayton完成签到 ,获得积分10
11秒前
柔弱山芙发布了新的文献求助10
11秒前
11秒前
科研小白发布了新的文献求助10
13秒前
14秒前
机灵的沂的应助被小恩采纳,获得10
14秒前
15秒前
17秒前
17秒前
20秒前
Caelifer发布了新的文献求助10
20秒前
路人发布了新的文献求助10
20秒前
21秒前
虬髯君关注了科研通微信公众号
21秒前
22秒前
jsnd完成签到,获得积分10
22秒前
22秒前
23秒前
淡淡泡芙发布了新的文献求助10
23秒前
科研小白完成签到,获得积分10
24秒前
orixero的应助被柚子采纳,获得10
25秒前
科研通AI2S的应助被lzy采纳,获得10
26秒前
26秒前
12138发布了新的文献求助10
26秒前
高分求助中
(应助此贴封号)通过应助OA文献获取积分 10000
Rosenblum, Global Change Biology 800
The Art of Interactive Teaching 600
Computational Chemical Reaction Engineering: Modeling, Simulation, and Design with MATLAB 600
Organizational Behavior 510
Management and the Arts 510
CLSI C56QG Examples of Hemolyzed, Icteric, and Lipemic/Turbid Samples Quick Guide 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 内科学 物理 有机化学 化学工程 生物化学 复合材料 光电子学 细胞生物学 心理学 量子力学 催化作用 物理化学 电极
热门帖子
关注 科研通微信公众号,转发送积分 7801071
求助须知:如何正确求助?哪些是违规求助? 9335592
关于积分的说明 20475095
捐赠科研通 7392623
什么是DOI,文献DOI怎么找? 3326497
关于科研通互助平台的介绍 2473408
邀请新用户注册赠送积分活动 2344334