Antiinflammatory therapies other than corticosteroids

Proc Am Thorac Soc. 2004;1(3):282-7. doi: 10.1513/pats.200402-020MS.


Antiinflammatory therapy for chronic obstructive pulmonary disease (COPD) can be directed at several stages of the inflammatory process. Much attention has been focused on blocking the damaging effects of toxic mediators released by inflammatory cells, including antioxidants and antiproteases. An alternate strategy is to block the recruitment of inflammatory cells into the lung, such as by inhibiting the production of chemotactic factors driving inflammatory cell recruitment, the ability of inflammatory cells to respond to chemotactic factors, and the ability of inflammatory cells to migrate. Moreover, mediators released by inflammatory cells, particularly tumor necrosis factor-alpha, probably have systemic effects in COPD. Blocking the release of these cytokines or blocking their ability to act on distal tissues represents another potential therapeutic option. It is also important to recognize that the various components of the inflammatory response are not independent. The action of proteases released by inflammatory cells, for example, can generate chemotactic factors, lead to activation of inflammatory cells, and modulate repair responses. The complex network of regulatory molecules that controls the inflammatory response, therefore, presents a number of potential therapeutic targets with the promise of altering the disease process in COPD.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use*
  • Chemotactic Factors
  • Cytokines / drug effects
  • Cytokines / metabolism
  • Humans
  • Inflammation Mediators / metabolism*
  • Leukocytes / drug effects*
  • Leukocytes / metabolism
  • Oxidative Stress / physiology
  • Pulmonary Disease, Chronic Obstructive / drug therapy*
  • Pulmonary Disease, Chronic Obstructive / physiopathology
  • Risk Factors
  • Sensitivity and Specificity
  • Severity of Illness Index
  • Treatment Outcome
  • Tumor Necrosis Factor-alpha / metabolism


  • Adrenal Cortex Hormones
  • Chemotactic Factors
  • Cytokines
  • Inflammation Mediators
  • Tumor Necrosis Factor-alpha