» Articles » PMID: 36451865

Development of Functional Nanomedicines for Tumor Associated Macrophages-focused Cancer Immunotherapy

Overview
Journal Theranostics
Date 2022 Dec 1
PMID 36451865
Authors
Affiliations
Soon will be listed here.
Abstract

Clinical cancer immunotherapies are usually impeded by tumor immunosuppression driven by tumor associated macrophages (TAMs). Thus, TAMs can be considered as a promising therapeutic target for improved immunotherapy, and TAMs-focused molecular targeting agents have made ideal progress in clinical practice. Even so, most TAMs-targeting agents still cannot cover up their own shortcomings as free drugs. The emergence of multifunctional nanomaterials can expectedly endow these therapeutic cargoes with high solubility, favorable pharmacokinetic distribution, cell-specific delivery, and controlled release. Here, the underlying mechanisms of tumor immunosuppression caused by TAMs are first emphatically elucidated, and then the basic design of TAMs-focused immune-nanomedicines are discussed, mainly including diverse categories of nanomaterials, targeted and stimulus-responsive modifications, and TAM imaging in nanomedicines. A summary of current TAMs-targeting immunotherapeutic mechanisms based on functional nanomedicines for TAMs elimination and/or repolarization is further presented. Lastly, some severe challenges related to functional nanomedicines for TAMs-focused cancer immunotherapy are proposed, and some feasible perspectives on clinical translation of TAMs-associated anticancer immunonanomedicines are provided. It is hoped that, with rapid development of nanomedicine in cancer immunotherapy, TAMs-focused therapeutic strategies may be anticipated to become an emerging immunotherapeutic modality for future clinical cancer treatment.

Citing Articles

Nanotherapeutics for Macrophage Network Modulation in Tumor Microenvironments: Targets and Tools.

Li R, Huang J, Wei Y, Wang Y, Lu C, Liu J Int J Nanomedicine. 2024; 19:13615-13651.

PMID: 39717515 PMC: 11665441. DOI: 10.2147/IJN.S491573.


Analysis of Lymphovascular Infiltration and Tumor-Associated Macrophages in Cervical Cancer Immunoescape.

Guan L, Xu X, Xu J, Xu G, Zhang Y, Xia H Onco Targets Ther. 2024; 17:1117-1136.

PMID: 39583248 PMC: 11585989. DOI: 10.2147/OTT.S468484.


Polypeptides-Based Nanocarriers in Tumor Therapy.

You J, Guo Y, Dong Z Pharmaceutics. 2024; 16(9).

PMID: 39339228 PMC: 11435007. DOI: 10.3390/pharmaceutics16091192.


Advances in nephroprotection: the therapeutic role of selenium, silver, and gold nanoparticles in renal health.

Karunakar K, Edwin E, Gopalakrishnan M, Cheriyan B, Ramaiyan V, Karthikha V Int Urol Nephrol. 2024; 57(2):479-510.

PMID: 39312019 DOI: 10.1007/s11255-024-04212-4.


Targeting tumor-associated macrophages with nanocarrier-based treatment for breast cancer: A step toward developing innovative anti-cancer therapeutics.

Muteeb G, Khafaga D, El-Morsy M, Farhan M, Aatif M, Hosney M Heliyon. 2024; 10(18):e37217.

PMID: 39309874 PMC: 11415663. DOI: 10.1016/j.heliyon.2024.e37217.


References
1.
Ding J, Zhao D, Hu Y, Liu M, Liao X, Zhao B . Terminating the renewal of tumor-associated macrophages: A sialic acid-based targeted delivery strategy for cancer immunotherapy. Int J Pharm. 2019; 571:118706. DOI: 10.1016/j.ijpharm.2019.118706. View

2.
Chen C, Jing W, Chen Y, Wang G, Abdalla M, Gao L . Intracavity generation of glioma stem cell-specific CAR macrophages primes locoregional immunity for postoperative glioblastoma therapy. Sci Transl Med. 2022; 14(656):eabn1128. DOI: 10.1126/scitranslmed.abn1128. View

3.
Chen Q, Wang C, Zhang X, Chen G, Hu Q, Li H . In situ sprayed bioresponsive immunotherapeutic gel for post-surgical cancer treatment. Nat Nanotechnol. 2018; 14(1):89-97. DOI: 10.1038/s41565-018-0319-4. View

4.
Heys S, Stewart K, McKenzie E, Miller I, Wong S, Sellar G . Characterisation of tumour-infiltrating macrophages: impact on response and survival in patients receiving primary chemotherapy for breast cancer. Breast Cancer Res Treat. 2012; 135(2):539-48. DOI: 10.1007/s10549-012-2190-6. View

5.
Elder M, Webster S, Williams D, Gaston J, Goodall J . TSLP production by dendritic cells is modulated by IL-1β and components of the endoplasmic reticulum stress response. Eur J Immunol. 2015; 46(2):455-63. PMC: 4783504. DOI: 10.1002/eji.201545537. View