Chronic inflammation within the vascular wall in pulmonary arterial hypertension: more than a spectator

Cardiovasc Res. 2020 Apr 1;116(5):885-893. doi: 10.1093/cvr/cvz308.

Abstract

This review seeks to provide an update of preclinical findings and available clinical data on the chronic persistent inflammation and its direct role on the pulmonary arterial hypertension (PAH) progression. We reviewed the different mechanisms by which the inflammatory and immune pathways contribute to the structural and functional changes occurring in the three vascular compartments: the tunica intima, tunica media, and tunica adventitia. We also discussed how these inflammatory mediator changes may serve as a biomarker of the PAH progression and summarize unanswered questions and opportunities for future studies in this area.

Keywords: Adventitial fibroblasts; Endothelial cells; Innate and adaptive immunity; Pulmonary hypertension; Pulmonary vascular remodelling; Smooth muscle cells.

Publication types

  • Review

MeSH terms

  • Adventitia / metabolism
  • Adventitia / pathology
  • Adventitia / physiopathology
  • Animals
  • Arterial Pressure*
  • Autoimmunity
  • Chronic Disease
  • Disease Progression
  • Humans
  • Inflammation Mediators / metabolism*
  • Pulmonary Arterial Hypertension / metabolism*
  • Pulmonary Arterial Hypertension / pathology
  • Pulmonary Arterial Hypertension / physiopathology
  • Pulmonary Artery / metabolism*
  • Pulmonary Artery / pathology
  • Pulmonary Artery / physiopathology
  • Signal Transduction
  • Tunica Intima / metabolism
  • Tunica Intima / pathology
  • Tunica Intima / physiopathology
  • Tunica Media / metabolism
  • Tunica Media / pathology
  • Tunica Media / physiopathology
  • Vascular Remodeling*
  • Vasculitis / metabolism*
  • Vasculitis / pathology
  • Vasculitis / physiopathology

Substances

  • Inflammation Mediators