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Interleukin 15 mediates joint destruction in staphylococcus aureus arthritis
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2012 (Engelska)Ingår i: Journal of Infectious Diseases, ISSN 0022-1899, E-ISSN 1537-6613, Vol. 206, nr 5, s. 687-696Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Background. Staphylococcus aureus arthritis causes severe and rapid joint damage despite antibiotics. Thus, there is a need to identify new treatment targets in addition to antibiotics. Lately, interleukin 15 (IL-15) has been implicated both in osteoclastogenesis and in bacterial clearance-2 important issues in S. aureus-induced joint destruction. This has prompted us to investigate the importance of IL-15 in S. aureus-induced arthritis.

Methods.Toxic shock syndrome toxin-1 producing S. aureus was intravenously inoculated in IL-15 knockout and wildtype mice and in wildtype mice treated with anti-IL-15 antibodies (aIL-15ab) or isotype control antibody.

Results. Absence of IL-15, either in knockout mice or after treatment with aIL-15ab, significantly reduced weight loss compared with controls during the infection. The severity of synovitis and joint destruction was significantly decreased in IL-15 knockout and aIL-15ab treated mice compared with controls. In IL-15 knockout mice there was a reduced number of osteoclasts in the joints. The host's ability to clear bacteria was not influenced in the IL-15 knockout mice, but significantly increased after treatment with aIL-15ab.

Conclusions. IL-15 is a mediator of joint destruction in S. aureus-induced arthritis and contributes to general morbidity, which makes this cytokine an interesting treatment target in addition to conventional antibiotics.

Ort, förlag, år, upplaga, sidor
2012. Vol. 206, nr 5, s. 687-696
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Odontologi
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URN: urn:nbn:se:umu:diva-59519DOI: 10.1093/infdis/jis295ISI: 000307501800009OAI: oai:DiVA.org:umu-59519DiVA, id: diva2:552969
Tillgänglig från: 2012-09-17 Skapad: 2012-09-17 Senast uppdaterad: 2018-06-08Bibliografiskt granskad

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Lerner, Ulf H

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