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Increased interleukin‐10 and macrophage inflammatoryprotein‐1α release from blood monocytes ex vivo duringlate‐phase response to allergen in asthma
Author(s) -
Lim S.,
John M.,
Seybold J.,
Taylor D.,
Witt C.,
Barnes P. J.,
Chung K. F.
Publication year - 2000
Publication title -
allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.363
H-Index - 173
eISSN - 1398-9995
pISSN - 0105-4538
DOI - 10.1034/j.1398-9995.2000.00483.x
Subject(s) - immunology , ex vivo , allergen , medicine , lipopolysaccharide , monocyte , asthma , interleukin , whole blood , allergy , in vivo , cytokine , biology , microbiology and biotechnology
Background: We determined the effect of late‐phase responses to allergen challenge of mildly allergic asthmatic patients on the expression and release of the cytokines IL‐10 and MIP‐1α from peripheral blood monocytes. Methods: Sixteen mildly allergic asthmatics were exposed to increasing concentrations of allergen aerosol. Nine demonstrated an early response alone (single responders), while seven had an early followed by a late response (dual responders). Monocytes were isolated from venous blood before and 24 h after allergen challenge, and placed in short‐term culture for determination ofIL‐10 mRNA expression by reverse‐transcription polymerase chain reactionand protein release. MIP‐1α protein release was measured byradioimmunoassay. Results: IL‐10 mRNA expression was significantly higher in dual responders than early responders alone, for unstimulated monocytes or for monocytes exposed to lipopolysaccharide or IL‐1β. In addition, the release of IL‐10 and MIP‐1α from monocytes of dual responders was also enhanced. Conclusions: Circulating monocytes are primed to release more of the cytokines, IL‐10 and MIP‐1α, in dual but not in single responders, at 24 h afterallergen. They may contribute to allergen‐induced inflammatory responsesin the airways.