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Beyond inflammation: airway epithelial cells are at the interface of innate and adaptive immunity

Journal

CURRENT OPINION IN IMMUNOLOGY
Volume 19, Issue 6, Pages 711-720

Publisher

CURRENT BIOLOGY LTD
DOI: 10.1016/j.coi.2007.08.004

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Funding

  1. NHLBI NIH HHS [R01 HL078860, R01 HL068546, R01 HL068546-24, R01 HL078860-01A1, R01 HL068546-22] Funding Source: Medline
  2. NIAID NIH HHS [1 R01 AI072570, R01 AI072570-01A1, R01 AI072570] Funding Source: Medline

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It has become increasingly clear that airway epithelial cells are central participants in innate and adaptive immune responses as well as mucosal inflammation. Epithelial cells produce antimicrobial host defense molecules, proinflammatory cytokines and chemokines in response to activation via pathogen recognition receptors. Recruitment of immune cells including dendritic cells, T cells and B cells into the proximity of epithelium results in the enhancement of adaptive immunity through interactions with epithelial cells. Newly identified epithelial-derived cytokines, including TSLP, IL-33 and BAFF, help to shape the local accumulation and activation of Th2 responses and B cell immunoglobulin production. Epithelial cells are also downstream targets of molecules that activate IL-13R and EGFR and are responsible for mucus production in both protective immune responses and allergic airway inflammatory diseases. Improved understanding of epithelial immune and inflammatory responses will hopefully suggest new strategies for therapeutic intervention.

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