Th17 cytokines: novel potential therapeutic targets for COPD pathogenesis and exacerbations - Archive ouverte HAL
Article Dans Une Revue European Respiratory Journal Année : 2017

Th17 cytokines: novel potential therapeutic targets for COPD pathogenesis and exacerbations

Olivier Le Rouzic
Muriel Pichavant
  • Fonction : Auteur
Emilie Frealle
  • Fonction : Auteur
Philippe Gosset

Résumé

Chronic obstructive pulmonary disease (COPD) is a chronic inflammatory disease of the airways caused mainly by cigarette smoke exposure. COPD progression is marked by exacerbations of the disease, often associated with infections. Recent data show the involvement in COPD pathophysiology of interleukin (IL)-17 and IL-22, two cytokines that are important in the control of lung inflammation and infection. During the initiation and progression of the disease, increased IL-17 secretion causes neutrophil recruitment, leading to chronic inflammation, airways obstruction and emphysema. In the established phase of COPD, a defective IL-22 response facilitates pathogen-associated infections and disease exacerbations. Altered production of these cytokines involves a complex network of immune cells and dysfunction of antigen-presenting cells. In this review, we describe current knowledge on the involvement of IL-17 and IL-22 in COPD pathophysiology at steady state and during exacerbations, and discuss implications for COPD management and future therapeutic approaches.

Dates et versions

hal-03601870 , version 1 (08-03-2022)

Identifiants

Citer

Olivier Le Rouzic, Muriel Pichavant, Emilie Frealle, Antoine Guillon, Mustapha Si-Tahar, et al.. Th17 cytokines: novel potential therapeutic targets for COPD pathogenesis and exacerbations. European Respiratory Journal, 2017, 50 (4), pp.1602434. ⟨10.1183/13993003.02434-2016⟩. ⟨hal-03601870⟩

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