Cytokine Circuits in Cardiovascular Disease

Immunity. 2019 Apr 16;50(4):941-954. doi: 10.1016/j.immuni.2019.03.007.

Abstract

Arterial inflammation is a hallmark of atherosclerosis, and appropriate management of this inflammation represents a major unmet therapeutic need for cardiovascular disease patients. Here, we review the diverse contributions of immune cells to atherosclerosis, the mechanisms of immune cell activation in this context, and the cytokine circuits that underlie disease progression. We discuss the recent application of these insights in the form of immunotherapy to treat cardiovascular disease and highlight how studies on the cardiovascular co-morbidity that arises in autoimmunity might reveal additional roles for cytokines in atherosclerosis. Currently, data point to interleukin-1β (IL-1β), tumor necrosis factor (TNF), and IL-17 as cytokines that, at least in some settings, are effective targets to reduce cardiovascular disease progression.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antibodies, Monoclonal / therapeutic use
  • Antibodies, Monoclonal, Humanized
  • Atherosclerosis / drug therapy
  • Atherosclerosis / immunology
  • Autoimmune Diseases / drug therapy
  • Autoimmune Diseases / immunology
  • Cardiovascular Diseases / drug therapy
  • Cardiovascular Diseases / immunology*
  • Cholesterol / metabolism
  • Clinical Trials as Topic
  • Cytokines / antagonists & inhibitors
  • Cytokines / immunology*
  • Cytokines / therapeutic use
  • Disease Progression
  • Foam Cells / immunology
  • Foam Cells / metabolism
  • Gastrointestinal Microbiome
  • Humans
  • Inflammasomes / immunology
  • Inflammation / drug therapy
  • Inflammation / immunology
  • Interleukin-1beta / antagonists & inhibitors
  • Mice, Knockout
  • Models, Immunological
  • Muscle, Smooth, Vascular / immunology
  • Phagocytes / immunology
  • Phagocytes / metabolism
  • Signal Transduction
  • Swine
  • Translational Research, Biomedical

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Cytokines
  • Inflammasomes
  • Interleukin-1beta
  • canakinumab
  • Cholesterol