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Cited by 1,085

The DOI matches its Crossref record; 99 of the 99 references it cites were found in a registry or an index.

Macrophage Polarization in Inflammatory Diseases

Open access
Liu, Yan-Cun, Zou, Xian-Biao, Chai, Yan-Fen, Yao, Yong-Ming·2014·International Journal of Biological Sciences

Abstract

Diversity and plasticity are two hallmarks of macrophages. M1 macrophages (classically activated macrophages) are pro-inflammatory and have a central role in host defense against infection, while M2 macrophages (alternatively activated macrophages) are associated with responses to anti-inflammatory reactions and tissue remodeling, and they represent two terminals of the full spectrum of macrophage activation. Transformation of different phenotypes of macrophages regulates the initiation, development, and cessation of inflammatory diseases. Here we reviewed the characters and functions of macrophage polarization in infection, atherosclerosis, obesity, tumor, asthma, and sepsis, and proposed that targeting macrophage polarization and skewing their phenotype to adapt to the microenvironment might hold great promise for the treatment of inflammatory diseases.

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Metadata

Authors
Liu, Y.-C., Zou, X.-B., Chai, Y.-F., & Yao, Y.-M.
Venue
International Journal of Biological Sciences
Published
2014
Volume
10
Issue
5
Pages
520-529
ISSN
1449-2288 (ISSN-L)
OpenAlex
W2100128950
Cited by
1,085
References
99
FWCI
16.60
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Macrophage Polarization in Inflammatory Diseases. https://app.cochat.ai/papers/10.7150/ijbs.8879
The paper
Liu, Y.-C., Zou, X.-B., Chai, Y.-F., & Yao, Y.-M. (2014). Macrophage Polarization in Inflammatory Diseases. International Journal of Biological Sciences. https://doi.org/10.7150/ijbs.8879

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.