| Literature DB >> 24447865 |
Elisa Tinazzi1, Alessandro Barbieri1, Antonella Rigo1, Giuseppe Patuzzo1, Ruggero Beri1, Roberto Gerli2, Giuseppe Argentino1, Antonio Puccetti3, Claudio Lunardi4.
Abstract
CD30 and CD30 ligand (CD30L) are members of TNF-receptor and TNF superfamilies respectively. CD30(+)T cells are increased in several diseases and interaction between CD30(+) and CD30L(+)T cells leads either to cell proliferation or apoptosis. In patients with rheumatoid arthritis (RA), soluble CD30 (sCD30) levels seem to reflect the recruitment of CD30(+)T cells into the inflamed joints and are predictive of a positive response to classical and biological immunosuppressive therapy. We have evaluated the presence of soluble CD30L (sCD30L) in the sera and synovial fluid of patients with RA and defined whether it binds surface CD30 molecule and is functionally active. We found high levels of sCD30L in sera and synovial fluid of RA patients; the molecule is shedded upon direct contact of CD30(+)/CD30L(+)T cells. Moreover sCD30L binds surface CD30 constitutively expressed by Jurkat cell line. Finally recombinant sCD30L and sera from patients with high levels of sCD30L are able to inhibit CD30(+)T cell proliferation by inducing cell apoptosis. Our findings suggest that circulant sCD30L is functionally active and that it may favor persistence of active inflammation by inducing apoptosis of CD30(+)T cells, known to down-modulate inflammation in rheumatoid synovitis.Entities:
Keywords: Apoptosis; CD30; CD30 ligand; Rheumatoid arthritis
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Year: 2014 PMID: 24447865 DOI: 10.1016/j.imlet.2014.01.007
Source DB: PubMed Journal: Immunol Lett ISSN: 0165-2478 Impact factor: 3.685