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Interleukin‐2 inhibits eosinophil migration but is counteracted by IL‐5 priming
Author(s) -
Lampinen M.,
Håkansson L.,
Venge P.
Publication year - 2001
Publication title -
clinical and experimental allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 154
eISSN - 1365-2222
pISSN - 0954-7894
DOI - 10.1046/j.1365-2222.2001.00968.x
Subject(s) - chemotaxis , eosinophil , eotaxin , cytokine , chemistry , priming (agriculture) , immunology , incubation , allergic inflammation , inflammation , immunogenicity , chemokine , antibody , biology , biochemistry , receptor , botany , germination , asthma
Conflicting data on the role of interleukin‐2 in the recruitment of eosinophil granulocytes (EOS) to sites of inflammation have been presented. The objective of the present study was to investigate the effect of recombinant human IL‐2 and anti‐IL‐2 on the migration of purified blood EOS. Neutralizing antibodies to IL‐2 were added to a cytokine mixture with significant eosinophil chemotactic activity (ECA), and afterwards the ECA was tested on EOS from both normal and allergic donors. EOS migration was measured by a modification of the Boyden technique, using a 48‐well microchemotaxis chamber. Recombinant human IL‐2 was either added to the lower compartment of the chemotaxis chamber, or to the EOS for a pre‐incubation period of 20 min, before migration assays towards the chemotaxins were performed. Anti‐IL‐2 caused a significant increase of EOS migration towards the cytokine mixture. Pre‐incubation of the EOS with rhIL‐2 inhibited the chemotaxis towards RANTES, PAF, IL‐8 and eotaxin, and EOS migration towards IL‐2 was lower than that towards buffer. These effects were more pronounced on EOS from normal than from allergic donors. Priming of the EOS with IL‐5 prevented the inhibitory effect of IL‐2. We hypothesize that IL‐2 acts as an autocrine regulator of EOS migration, and that this inhibitory effect may be downregulated in allergy, allowing an increased migration of EOS towards chemotactic factors.