Macrophage-Based Therapies for Atherosclerosis Management
Atherosclerosis (AS), a typical chronic inflammatory vascular disease, is the main pathological basis of ischemic cardio/cerebrovascular disease (CVD). Long-term administration was characterized with low efficacy and serious side effects, while the macrophages with attractive intrinsic homing target...
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Published in | Journal of Immunology Research Vol. 2020; no. 2020; pp. 1 - 11 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cairo, Egypt
Hindawi Publishing Corporation
2020
Hindawi John Wiley & Sons, Inc Wiley |
Subjects | |
Online Access | Get full text |
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Abstract | Atherosclerosis (AS), a typical chronic inflammatory vascular disease, is the main pathological basis of ischemic cardio/cerebrovascular disease (CVD). Long-term administration was characterized with low efficacy and serious side effects, while the macrophages with attractive intrinsic homing target have great potential in the efficient and safe management of AS. In this review, we focused on the systematical summary of the macrophage-based therapies in AS management, including macrophage autophagy, polarization, targeted delivery, microenvironment-triggered drug release, and macrophage- or macrophage membrane-based drug carrier. In conclusion, macrophage-based therapies have great promise to effectively manage AS in future research and clinic translation. |
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AbstractList | Atherosclerosis (AS), a typical chronic inflammatory vascular disease, is the main pathological basis of ischemic cardio/cerebrovascular disease (CVD). Long-term administration was characterized with low efficacy and serious side effects, while the macrophages with attractive intrinsic homing target have great potential in the efficient and safe management of AS. In this review, we focused on the systematical summary of the macrophage- based therapies in AS management, including macrophage autophagy, polarization, targeted delivery, microenvironment- triggered drug release, and macrophage- or macrophage membrane-based drug carrier. In conclusion, macrophage-based therapies have great promise to effectively manage AS in future research and clinic translation. Atherosclerosis (AS), a typical chronic inflammatory vascular disease, is the main pathological basis of ischemic cardio/cerebrovascular disease (CVD). Long-term administration was characterized with low efficacy and serious side effects, while the macrophages with attractive intrinsic homing target have great potential in the efficient and safe management of AS. In this review, we focused on the systematical summary of the macrophage-based therapies in AS management, including macrophage autophagy, polarization, targeted delivery, microenvironment-triggered drug release, and macrophage- or macrophage membrane-based drug carrier. In conclusion, macrophage-based therapies have great promise to effectively manage AS in future research and clinic translation.Atherosclerosis (AS), a typical chronic inflammatory vascular disease, is the main pathological basis of ischemic cardio/cerebrovascular disease (CVD). Long-term administration was characterized with low efficacy and serious side effects, while the macrophages with attractive intrinsic homing target have great potential in the efficient and safe management of AS. In this review, we focused on the systematical summary of the macrophage-based therapies in AS management, including macrophage autophagy, polarization, targeted delivery, microenvironment-triggered drug release, and macrophage- or macrophage membrane-based drug carrier. In conclusion, macrophage-based therapies have great promise to effectively manage AS in future research and clinic translation. |
Audience | Academic |
Author | Huang, Yijiang Jin, Libo Sun, Da Xu, Ke Lin, Sue Ji, Hao Wu, Wei Peng, Renyi Yang, Qinsi |
AuthorAffiliation | 3 Department of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325027, China 1 Institute of Life Sciences, Wenzhou University, Wenzhou, Zhejiang 325035, China 5 Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing 400030, China 2 Biomedical Collaborative Innovation Center of Zhejiang Province & Engineering Laboratory of Zhejiang Province for Pharmaceutical Development of Growth Factors, Biomedical Collaborative Innovation Center of Wenzhou, Wenzhou, Zhejiang 325035, China 4 Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, Zhejiang 325000, China |
AuthorAffiliation_xml | – name: 3 Department of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325027, China – name: 1 Institute of Life Sciences, Wenzhou University, Wenzhou, Zhejiang 325035, China – name: 5 Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing 400030, China – name: 4 Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, Zhejiang 325000, China – name: 2 Biomedical Collaborative Innovation Center of Zhejiang Province & Engineering Laboratory of Zhejiang Province for Pharmaceutical Development of Growth Factors, Biomedical Collaborative Innovation Center of Wenzhou, Wenzhou, Zhejiang 325035, China |
Author_xml | – sequence: 1 fullname: Wu, Wei – sequence: 2 fullname: Sun, Da – sequence: 3 fullname: Xu, Ke – sequence: 4 fullname: Huang, Yijiang – sequence: 5 fullname: Lin, Sue – sequence: 6 fullname: Jin, Libo – sequence: 7 fullname: Ji, Hao – sequence: 8 fullname: Peng, Renyi – sequence: 9 fullname: Yang, Qinsi |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32411803$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | Copyright © 2020 Renyi Peng et al. COPYRIGHT 2020 John Wiley & Sons, Inc. Copyright © 2020 Renyi Peng et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 Copyright © 2020 Renyi Peng et al. 2020 |
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SubjectTerms | Animals Apoptosis Arteriosclerosis Atherosclerosis Atherosclerosis - drug therapy Atherosclerosis - immunology Autophagy Autophagy - drug effects Autophagy - immunology Blood circulation disorders Cardiovascular Agents - pharmacology Cardiovascular Agents - therapeutic use Cardiovascular disease Cell Membrane - drug effects Cell Membrane - immunology Cerebrovascular diseases Cholesterol Coronary heart disease Disease Models, Animal Drug Carriers - pharmacology Drug delivery systems Drugs Gene expression Humans Immunology Inflammasomes - drug effects Inflammasomes - immunology Inflammation Ischemia Kinases Lipids Lipoproteins Macrophage Activation - drug effects Macrophage Activation - immunology Macrophages Macrophages - cytology Macrophages - drug effects Macrophages - immunology Management Oxidative stress Pathogenesis Phagocytosis Proteins Review Vascular diseases Vehicles |
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Title | Macrophage-Based Therapies for Atherosclerosis Management |
URI | https://search.emarefa.net/detail/BIM-1187523 https://dx.doi.org/10.1155/2020/8131754 https://www.ncbi.nlm.nih.gov/pubmed/32411803 https://www.proquest.com/docview/2352591207 https://www.proquest.com/docview/2404050692 https://pubmed.ncbi.nlm.nih.gov/PMC7204102 https://doaj.org/article/80ae946d5bb249b4ae88e0c093b71445 |
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