Idiopathic and autoimmune interstitial lung disease

Brian Gelbman, Ronald G. Crystal

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Interstitial lung disease is a broad category of heterogenous diseases which share the common feature of inflammatory and fibrotic changes that primarily affect the alveoli and small airways. The two most common manifestations are cryptogenic organizing pneumonia (COP) and idiopathic pulmonary fibrosis (IPF), both of which can occur as “idiopathic” conditions or in association with several autoimmune diseases. Although both are classified as “lung disorders of unknown etiology,” there are multiple clues suggesting that autoimmune mechanisms play a role in the pathogenesis of both disorders. The focus of this chapter is to explore the link between autoimmune mechanisms underlying COP and IPF as models for autoimmune disorders of the lung. To do so, we discuss the history and the clinical features of COP and IPF, followed by a summary of the autoimmune, genetic, environmental features, current concepts of pathogenesis, and the therapies currently available and under investigation for both disorders.

Original languageEnglish
Title of host publicationThe Autoimmune Diseases
PublisherElsevier
Pages1335-1354
Number of pages20
ISBN (Electronic)9780128121023
ISBN (Print)9780128122426
DOIs
Publication statusPublished - 1 Jan 2019

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Keywords

  • Acute respiratory distress syndrome
  • Antinuclear antibodies
  • Bronchiolitis obliterans
  • Bronchoalveolar lavage
  • Cryptogenic organizing pneumonia
  • High-resolution computed tomography
  • Idiopathic pulmonary fibrosis
  • Rheumatoid arthritis

ASJC Scopus subject areas

  • Medicine(all)
  • Immunology and Microbiology(all)

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