Targeting tumor associated macrophages: The new challenge for nanomedicine

被引:105
作者
Andon, Fernando Torres [1 ,2 ]
Digifico, Elisabeth [1 ,3 ]
Maeda, Akihiro [1 ]
Erreni, Marco [1 ]
Mantovani, Alberto [1 ,3 ]
Jose Alonso, Maria [2 ,4 ,5 ]
Allavena, Paola [1 ]
机构
[1] IRCCS, Ist Clin Humanitas, Via A Manzoni 113, I-20089 Milan, Italy
[2] Univ Santiago de Compostela, Ctr Res Mol Med & Chron Dis CIMUS, Campus Vida, Santiago De Compostela 15706, Spain
[3] Humanitas Univ, Via A Manzoni 113, I-20089 Milan, Italy
[4] Univ Santiago de Compostela, Sch Pharm, Pharm & Pharmaceut Technol Dept, Campus Vida, Santiago De Compostela 15705, Spain
[5] Hlth Res Inst Santiago de Compostela IDIS, Santiago De Compostela 15706, Spain
关键词
Nanomedicine; Tumor associated macrophages; Cancer immunotherapy; Mononuclear phagocyte system; Drug delivery; Tumor microenvironment; IMPROVING DRUG-DELIVERY; INDUCIBLE FACTOR-I; ANTIANGIOGENIC THERAPY; INFLAMMATORY MONOCYTES; NANOPARTICLES INHIBIT; CLINICAL-SIGNIFICANCE; MACROMOLECULAR DRUG; ANTITUMOR-ACTIVITY; SUPPRESSOR-CELLS; BLOOD-VESSELS;
D O I
10.1016/j.smim.2017.09.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The engineering of new nanomedicines with ability to target and kill or re-educate Tumor Associated Macrophages (TAMS) stands up as a promising strategy to induce the effective switching of the tumor-promoting immune suppressive microenvironment, characteristic of tumors rich in macrophages, to one that kills tumor cells, is anti-angiogenic and promotes adaptive immune responses. Alternatively, the loading of monocytes/macrophages in blood circulation with nanomedicines, may be used to profit from the high infiltration ability of myeloid cells and to allow the drug release in the bulk of the tumor. In addition, the development of TAM-targeted imaging nanostructures, can be used to study the macrophage content in solid tumors and, hence, for a better diagnosis and prognosis of cancer disease. The major challenges for the effective targeting of TAM with nanomedicines and their application in the clinic have already been identified. These challenges are associated to the undesirable clearance of nanomedicines by, the mononuclear phagocyte system (macrophages) in competing organs (liver, lung or spleen), upon their intravenous injection; and also to the difficult penetration of nanomedicines across solid tumors due to the abnormal vasculature and the excessive extracellular matrix present in stromal tumors. In this review we describe the recent nanotechnology-base strategies that have been developed to target macrophages in tumors.
引用
收藏
页码:103 / 113
页数:11
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