Chemoattraction of Human T Cells by IL-18
Author(s) -
Mousa KomaiKoma,
J. Alastair Gracie,
XiaoQing Wei,
Damo Xu,
Neil C. Thomson,
Iain B. McInnes,
Foo Y. Liew
Publication year - 2003
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.170.2.1084
Subject(s) - cytokine , ex vivo , immune system , t cell , immunology , microbiology and biotechnology , in vitro , rheumatoid arthritis , inflammation , chemotaxis , arthritis , t lymphocyte , in vivo , biology , chemistry , medicine , receptor , biochemistry
Cell locomotion is crucial to the induction of an effective immune response. We report here the chemoattraction of CD4(+) T cells by IL-18, a member of the IL-1 cytokine family. Recombinant IL-18 increased the proportion of T cells in polarized morphology in vitro and stimulated their subsequent invasion into collagen gels in an IL-18 concentration gradient-dependent manner. Immunofluorescent microscopy studies determined that the major cell type responding to IL-18 was IL-18R(+)CD4(+). Importantly, synovial CD4(+) T cells from patients with rheumatoid arthritis responded to IL-18, adopting polarized morphology and gel invasion without further activation ex vivo, indicating the physiologic relevance of our observations. Finally, injection of rIL-18 into the footpad of DBA/1 mice led to local accumulation of inflammatory cells. These data therefore demonstrate for the first time lymphocyte chemoattractant properties of a member of the IL-1 cytokine family and its relevance in inflammatory diseases.
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