Endothelial lineage-specific interaction of Mycobacterium tuberculosis with the blood and lymphatic systems

Tuberculosis (Edinb). 2018 Jul:111:1-7. doi: 10.1016/j.tube.2018.04.009. Epub 2018 May 4.

Abstract

Mycobacterium tuberculosis (Mtb) has plagued humanity for tens of thousands of years, yet still remains a threat to human health. Its pathology is largely associated with pulmonary tuberculosis with symptoms including fever, hemoptysis, and chest pain. Mtb, however, also manifests in other extrapulmonary organs, such as the pleura, bones, gastrointestinal tract, central nervous system, and lymph nodes. Compared to the knowledge of pulmonary tuberculosis, extrapulmonary pathologies of Mtb are quite understudied. Lymph node tuberculosis is one of the most common extrapulmonary manifestations of tuberculosis, and presents significant challenges in its diagnosis, management, and treatment due to its elusive etiologies and pathologies. The objective of this review is to overview the current understanding of the tropism and pathogenesis of Mtb in endothelial cells of the extrapulmonary tissues, particularly, in lymph nodes. Lymphatic endothelial cells (LECs) are derived from blood vascular endothelial cells (BECs) during development, and these two types of endothelial cells demonstrate substantial molecular, cellular and genetic similarities. Therefore, systemic comparison of the differential and common responses of BECs vs. LECs to Mtb invasion could provide new insights into its pathogenesis, and may promote new investigations into this deadly disease.

Keywords: Extrapulmonary tuberculosis; Host-directed chemotherapy; Lymphatic endothelial cells; Vascular endothelial cells.

Publication types

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

MeSH terms

  • Animals
  • Antitubercular Agents / therapeutic use
  • Biomarkers / metabolism
  • Cell Lineage*
  • Endothelial Cells / drug effects
  • Endothelial Cells / immunology
  • Endothelial Cells / metabolism
  • Endothelial Cells / microbiology*
  • Endothelium, Lymphatic / drug effects
  • Endothelium, Lymphatic / immunology
  • Endothelium, Lymphatic / metabolism
  • Endothelium, Lymphatic / microbiology*
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / immunology
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / microbiology*
  • Host-Pathogen Interactions
  • Humans
  • Mycobacterium tuberculosis / drug effects
  • Mycobacterium tuberculosis / immunology
  • Mycobacterium tuberculosis / metabolism
  • Mycobacterium tuberculosis / pathogenicity*
  • Phenotype
  • Signal Transduction
  • Tuberculosis / drug therapy
  • Tuberculosis / immunology
  • Tuberculosis / metabolism
  • Tuberculosis / microbiology*

Substances

  • Antitubercular Agents
  • Biomarkers