Abstract

Chronic atopic asthma in adulthood represents the end stage of a disease process that is initiated during the perinatal period, when the naive immune system is first confronted with potentially allergenic airborne antigens. The initial phase involves compartmentalization of immunological memory into either the T-helper (Th)-1 or Th2 cytokine phenotypes, in atopic and nonatopics, respectively, and in a subset of atopics, this results in chronic Th2 cytokine-driven inflammation in the airways. Dendritic cells appear to play a key role in directing the memory generation process, and in subsequently controlling the intensity and duration of the ensuing Th-cell responses responsible for this inflammation.

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