The Role of Macrophages in Connective Tissue Disease-Associated Interstitial Lung Disease: Focusing on Molecular Mechanisms and Potential Treatment Strategies

Int J Mol Sci. 2023 Jul 26;24(15):11995. doi: 10.3390/ijms241511995.

Abstract

Connective tissue disease-associated interstitial lung disease (CTD-ILD) is a severe manifestation of CTD that leads to significant morbidity and mortality. Clinically, ILD can occur in diverse CTDs. Pathologically, CTD-ILD is characterized by various histologic patterns, such as nonspecific interstitial pneumonia, organizing pneumonia, and usual interstitial pneumonia. Abnormal immune system responses have traditionally been instrumental in its pathophysiology, and various changes in immune cells have been described, especially in macrophages. This article first briefly overviews the epidemiology, clinical characteristics, impacts, and histopathologic changes associated with CTD-ILD. Next, it summarizes the roles of various signaling pathways in macrophages or products of macrophages in ILD, helped by insights gained from animal models. In the following sections, this review returns to studies of macrophages in CTD-ILD in humans for an overall picture of the current understanding. Finally, we direct attention to potential therapies targeting macrophages in CTD-ILD in investigation or in clinical trials, as well as the future directions regarding macrophages in the context of CTD-ILD. Although the field of macrophages in CTD-ILD is still in its infancy, several lines of evidence suggest the potential of this area.

Keywords: connective tissue disease; interstitial lung disease; macrophage; systemic sclerosis.

Publication types

  • Review

MeSH terms

  • Animals
  • Connective Tissue Diseases* / complications
  • Humans
  • Idiopathic Interstitial Pneumonias*
  • Idiopathic Pulmonary Fibrosis* / complications
  • Lung Diseases, Interstitial* / complications
  • Lung Diseases, Interstitial* / therapy
  • Macrophages

Grants and funding

This research received no external funding.