Nanomedicines for Dysfunctional Macrophage-Associated Diseases
Abstract
Macrophages play vital functions in host inflammatory reaction, tissue repair, homeostasis and immunity. Dysfunctional macrophages have significant pathophysiological impacts on diseases such as cancer, inflammatory diseases (rheumatoid arthritis and inflammatory bowel disease), metabolic diseases (atherosclerosis, diabetes and obesity) and major infections like human immunodeficiency virus infection. In view of this common etiology in these diseases, targeting the recruitment, activation and regulation of dysfunctional macrophages represents a promising therapeutic strategy. With the advancement of nanotechnology, development of nanomedicines to efficiently target dysfunctional macrophages can strengthen the effectiveness of therapeutics and improve clinical outcomes. This review discusses the specific roles of dysfunctional macrophages in various diseases and summarizes the latest advances in nanomedicine-based therapeutics and theranostics for treating diseases associated with dysfunctional macrophages.
Recommended Citation
H. He et al., "Nanomedicines for Dysfunctional Macrophage-Associated Diseases," Journal of Controlled Release, vol. 247, pp. 106 - 126, Elsevier B.V., Feb 2017.
The definitive version is available at https://doi.org/10.1016/j.jconrel.2016.12.032
Department(s)
Chemical and Biochemical Engineering
Keywords and Phrases
Cell receptor; Drug delivery; Gene therapy; In vivo; Macrophage phenotype; Tissue macrophages
International Standard Serial Number (ISSN)
0168-3659; 1873-4995
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2017 Elsevier B.V., All rights reserved.
Publication Date
10 Feb 2017
PubMed ID
28057522
Comments
This work was supported by VCU's CTSA award (UL1TR000058) from the National Center for Advancing Translational Sciences and the CCTR Endowment Fund of Virginia Commonwealth University to HY and SG as well as National Science Foundation CAREER award (CBET0954957) (HY).