4.1 Review

Has the time come to rethink the pathogenesis of asthma?

Journal

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/ACI.0b013e3283347be5

Keywords

allergens; asthma; epithelium; inflammation; mesenchyme; remodelling; virus infection

Funding

  1. Medical Research Council
  2. Asthma UK
  3. Asthma, Allergy Inflammation and Repair (AAIR)
  4. British Lung Foundation
  5. MRC [G19/34, G0800766, G0501506] Funding Source: UKRI
  6. Medical Research Council [G19/34, G0800766, G0501506] Funding Source: researchfish

Ask authors/readers for more resources

Purpose of review To explore new ground in asthma pathogenesis. Asthma is an inflammatory disorder of the airways that has strong association with allergy as characterized by a Th2-type T cell response. However, ranges of approaches that have targeted this immunological component have so far been disappointing. Most asthma therapy still relies on bronchodilators and corticosteroids rather than treating underlying disease mechanisms. Recent findings In this review, a case is made that asthma has its primary origin in the airways that involves defective behaviour of the epithelium in relation to environmental exposures. These include defects in barrier function and an impaired innate immunity to provide the substrate upon which allergic sensitization can occur. Once the airways are sensitized repeated allergen exposure leads to disease persistence. Such mechanisms could explain airway wall remodelling and the susceptibility of the asthmatic lung to exacerbations provoked by viruses, air pollution, certain drugs, and biologically active allergens. Summary Activation of the epithelial-mesenchymal trophic unit could be responsible for the emergence of different asthma phenotypes and direct a more targeted approach to treatment. There is also the possibility of developing treatments that increase the lung's resistance to the inhaled environment rather than focusing on the suppression of inflammation once established.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available