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Targeted nanomedicines remodeling immunosuppressive tumor microenvironment for enhanced cancer immunotherapy.

作者信息

Xu Yanyan, Xiong Jingyuan, Sun Xiyang, Gao Huile

机构信息

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

Healthy Food Evaluation Research Center, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Acta Pharm Sin B. 2022 Dec;12(12):4327-4347. doi: 10.1016/j.apsb.2022.11.001. Epub 2022 Nov 4.


DOI:10.1016/j.apsb.2022.11.001
PMID:36561994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9764075/
Abstract

Cancer immunotherapy has significantly flourished and revolutionized the limited conventional tumor therapies, on account of its good safety and long-term memory ability. Discouragingly, low patient response rates and potential immune-related side effects make it rather challenging to literally bring immunotherapy from bench to bedside. However, it has become evident that, although the immunosuppressive tumor microenvironment (TME) plays a pivotal role in facilitating tumor progression and metastasis, it also provides various potential targets for remodeling the immunosuppressive TME, which can consequently bolster the effectiveness of antitumor response and tumor suppression. Additionally, the particular characteristics of TME, in turn, can be exploited as avenues for designing diverse precise targeting nanomedicines. In general, it is of urgent necessity to deliver nanomedicines for remodeling the immunosuppressive TME, thus improving the therapeutic outcomes and clinical translation prospects of immunotherapy. Herein, we will illustrate several formation mechanisms of immunosuppressive TME. More importantly, a variety of strategies concerning remodeling immunosuppressive TME and strengthening patients' immune systems, will be reviewed. Ultimately, we will discuss the existing obstacles and future perspectives in the development of antitumor immunotherapy. Hopefully, the thriving bloom of immunotherapy will bring vibrancy to further exploration of comprehensive cancer treatment.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/f88e0da5f2c3/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/56fadde68024/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/704478149a3d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/1a2be7a995b5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/437a297143ea/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/6ecaee2bc51e/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/809666b79064/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/ff881b2b8305/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/5470a4f2d571/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/f88e0da5f2c3/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/56fadde68024/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/704478149a3d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/1a2be7a995b5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/437a297143ea/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/6ecaee2bc51e/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/809666b79064/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/ff881b2b8305/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/5470a4f2d571/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e84/9764075/f88e0da5f2c3/gr8.jpg

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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Remodeling "cold" tumor immune microenvironment epigenetic-based therapy using targeted liposomes with formed albumin corona.

Acta Pharm Sin B. 2022-4

[2]
Toll-like receptor (TLR) agonists as a driving force behind next-generation vaccine adjuvants and cancer therapeutics.

Curr Opin Chem Biol. 2022-10

[3]
Myeloid derived suppressor cells and innate immune system interaction in tumor microenvironment.

Life Sci. 2022-9-15

[4]
A BRD4 PROTAC nanodrug for glioma therapy the intervention of tumor cells proliferation, apoptosis and M2 macrophages polarization.

Acta Pharm Sin B. 2022-6

[5]
Nano-delivery of salvianolic acid B induces the quiescence of tumor-associated fibroblasts via interfering with TGF-β1/Smad signaling to facilitate chemo- and immunotherapy in desmoplastic tumor.

Int J Pharm. 2022-7-25

[6]
Targeted regulation of tumor microenvironment through the inhibition of MDSCs by curcumin loaded self-assembled nano-filaments.

Mater Today Bio. 2022-5-25

[7]
Delivery of an ectonucleotidase inhibitor with ROS-responsive nanoparticles overcomes adenosine-mediated cancer immunosuppression.

Sci Transl Med. 2022-6-8

[8]
Metabolic reprogramming by dual-targeting biomimetic nanoparticles for enhanced tumor chemo-immunotherapy.

Acta Biomater. 2022-8

[9]
Restoration of the Immunogenicity of Tumor Cells for Enhanced Cancer Therapy via Nanoparticle-Mediated Copper Chaperone Inhibition.

Angew Chem Int Ed Engl. 2022-8-1

[10]
Cancer Immunoediting in the Era of Immuno-oncology.

Clin Cancer Res. 2022-9-15

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