Declining Pulmonary Function in Interstitial Lung Disease Linked to Lymphocyte Dysfunction

Am J Respir Crit Care Med. 2020 Mar 1;201(5):610-613. doi: 10.1164/rccm.201910-1909LE.
No abstract available

Publication types

  • Letter
  • Meta-Analysis
  • Research Support, N.I.H., Extramural

MeSH terms

  • CD40 Ligand / genetics
  • Disease Progression
  • GATA3 Transcription Factor / genetics
  • Gene Expression
  • Humans
  • Idiopathic Pulmonary Fibrosis / genetics
  • Idiopathic Pulmonary Fibrosis / immunology*
  • Idiopathic Pulmonary Fibrosis / physiopathology
  • Ikaros Transcription Factor / genetics
  • Inducible T-Cell Co-Stimulator Protein / genetics
  • Lymphocytes / immunology*
  • Lymphocytes / metabolism
  • Nuclear Receptor Subfamily 1, Group F, Member 1 / genetics
  • Pulmonary Diffusing Capacity
  • Receptors, CCR4 / genetics
  • Receptors, CCR6 / genetics
  • Receptors, CCR7 / genetics
  • Sarcoidosis, Pulmonary / genetics
  • Sarcoidosis, Pulmonary / immunology*
  • Sarcoidosis, Pulmonary / physiopathology
  • T-Box Domain Proteins / genetics
  • T-bet Transcription Factor
  • Vital Capacity

Substances

  • CCR4 protein, human
  • CCR6 protein, human
  • CCR7 protein, human
  • EOMES protein, human
  • GATA3 Transcription Factor
  • GATA3 protein, human
  • ICOS protein, human
  • IKZF3 protein, human
  • Inducible T-Cell Co-Stimulator Protein
  • Nuclear Receptor Subfamily 1, Group F, Member 1
  • RORA protein, human
  • Receptors, CCR4
  • Receptors, CCR6
  • Receptors, CCR7
  • T-Box Domain Proteins
  • T-bet Transcription Factor
  • CD40 Ligand
  • Ikaros Transcription Factor