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.

Journal of Vascular Surgery
|December 29, 2018
PubMed

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.
Abstract

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