Screening for new macrophage therapeutics

被引:53
作者
Rodell, Christopher B. [1 ]
Koch, Peter D. [1 ,2 ]
Weissleder, Ralph [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Ctr Syst Biol, 185 Cambridge St,CPZN 5206, Boston, MA 02114 USA
[2] Harvard Med Sch, Dept Syst Biol, 200 Longwood Ave, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
macrophage therapeutics; screening; TUMOR-ASSOCIATED MACROPHAGES; CYTOKINE REPORTER MICE; IMMUNE CELLS; CANCER; INFLAMMATION; ATHEROSCLEROSIS; EXPRESSION; RESPONSES; MURINE; DIFFERENTIATION;
D O I
10.7150/thno.34421
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Myeloid derived macrophages play a key role in many human diseases, and their therapeutic modulation via pharmacological means is receiving considerable attention. Of particular interest is the fact that these cells are i) dynamic phenotypes well suited to therapeutic manipulation and ii) phagocytic, allowing them to be efficiently targeted with nanoformulations. However, it is important to consider that macrophages represent heterogeneous populations of subtypes with often competing biological behaviors and functions. In order to develop next generation therapeutics, it is therefore essential to screen for biological effects through a combination of in vitro and in vivo assays. Here, we review the state-of-the-art techniques, including both cell based screens and in vivo imaging tools that have been developed for assessment of macrophage phenotype. We conclude with a forward-looking perspective on the growing need for noninvasive macrophage assessment and laboratory assays to be put into clinical practice and the potential broader impact of myeloid-targeted therapeutics.
引用
收藏
页码:7714 / 7729
页数:16
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