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Article
Nature Medicine  3, 189 - 195 (1997)
doi:10.1038/nm0297-189

Interleukin-15 mediates T cell-dependent regulation of tumor necrosis factor-alpha production in rheumatoid arthritis

Iain B. McInnes1, 2, Bernard P. Leung1, Roger D. Sturrock2, Max Field2 & Foo Y. Liew1, 3

  1Department of Immunology, University Department of Medicine, University of Glasgow, Glasgow, G11 6NT, UK

  2Centre for Rheumatic Diseases, University Department of Medicine, University of Glasgow, Glasgow, G11 6NT, UK

  3Correspondence should be addressed to F.Y.L.

Tumor necrosis factor-alpha occupies a central role in rheumatoid arthritis (RA) pathogenesis. We now report that Interleukin-15 (IL-15) can induce TNF-alpha production in RA through activation of synovial T cells. Peripheral blood (PB) T cells activated by IL-15 induced significant TNF-alpha production by macrophages via a cell-contact-dependent mechanism. Freshly isolated RA synovial T cells possessed similar capability, and in vitro, IL-15 was necessary to maintain this activity. IL-15 also induced direct TNF-alpha production by synovial T cells. In contrast, IL-2 induced significantly lower TNF-alpha production in either cell-contact-dependent or direct culture, and IL-8 and MIP-1alpha were ineffective. Antibodies against C069, LFA-1 or ICAM-1 significantly inhibited the ability of T cells to activate macrophages by cell contact.

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ISSN: 1078-8956
EISSN: 1546-170X
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