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Synthesis of Monocyte-targeting Peptide Amphiphile Micelles for Imaging of Atherosclerosis
Published on: November 17, 2017
Recent advances in therapeutic targeting of inflammation in atherosclerosis
Ulf Hedin1, Ljubica Perisic Matic1
1Departments of Vascular Surgery and Molecular Medicine and Surgery, Karolinska University Hospital and the Karolinska Institute, Stockholm, Sweden.
Insights
Future peripheral vascular disease (PVD) prevention may target inflammation. Research highlights how targeting inflammation, through immune cell modulation and anti-inflammatory drugs, can improve cardiovascular risk and PVD treatment.
Area of Science:
- Cardiovascular Research
- Immunology
- Pharmacology
Background:
- Current peripheral vascular disease (PVD) prevention emphasizes blood pressure, lipids, and platelet inhibition.
- Inflammation's role in atherosclerosis pathophysiology is well-established, yet its targeted management in PVD is emerging.
- Statins and aspirin possess anti-inflammatory properties, prompting increased focus on inflammation as a therapeutic target.
Purpose of the Study:
- To summarize recent clinical and translational discoveries for future inflammation-targeted therapies in PVD.
- To review common inflammatory features across cardiovascular, cancer, and autoimmune diseases for shared therapeutic strategies.
- To highlight advancements in PVD research focusing on inflammation, including genetic factors, biological pharmaceuticals, and immune-mediated clearance.
Main Methods:
- A PubMed search utilized MeSH terms: inflammation, pathophysiology, atherosclerosis, cancer, autoimmune disease, therapy, and clinical trial.
- Literature selection prioritized basic inflammation pathophysiology and clinical investigations targeting inflammation in diverse diseases.
- Focus was placed on cardiovascular disease, cancer, and autoimmune disease clinical trials and translational studies.
Main Results:
- Common inflammatory features across diseases suggest potential for unified therapeutic strategies.
- Hematopoietic mutations increasing immune cell activity correlate with higher cardiovascular risk.
- Anti-inflammatory biological pharmaceuticals demonstrate efficacy in reducing cardiovascular risk.
- Targeting defective immune-mediated clearance of cellular debris in lesions may prevent disease progression.
Conclusions:
- Atherosclerosis research advancements are bringing inflammation into clinical focus for PVD.
- Discoveries in cardiovascular risk prediction and inflammation-targeted pharmacotherapy offer future PVD care improvements.
Objective:
Current prevention of peripheral vascular disease (PVD) focuses on blood pressure control, lipid lowering, and platelet inhibition with statins and aspirin. A critical role for inflammation in the pathophysiology of atherosclerosis has been established for decades and, although both statins and aspirin have anti-inflammatory properties, the management of inflammation is becoming increasingly recognized. Here, we summarize recent clinical and translational discoveries that outline how inflammation may become targeted in PVD in the future.
Methods:
A PubMed search using a combination of the following MeSH terms-inflammation, pathophysiology, atherosclerosis, cancer, auto immune disease, therapy, and clinical trial-was performed and literature selected with a focus on basic pathophysiology of inflammation and clinical investigations targeting inflammation in cardiovascular disease, cancer, and autoimmune diseases.
Results:
Based on this literature overview, we summarized the common features of inflammation in these different diseases and how inflammation may also translate into common therapeutic strategies. Finally, the results of recent clinical and translational investigations highlighting inflammation in cardiovascular disease are reviewed with a focus on hematopoietic mutations that generate more active immune cells and increase cardiovascular risk, treatment with anti-inflammatory biological pharmaceuticals that reduce cardiovascular risk, and translational studies demonstrating how the treatment of defective immune-mediated clearance of dying cells in lesions may prevent disease progression.
Conclusions:
Progress in clinical and translational atherosclerosis research has now brought inflammation in clinical focus, because recent discoveries with respect to cardiovascular risk prediction and pharmacotherapy targeting inflammation have shown the potential to improve future care of patients with PVD.
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