Specificity of T cells in synovial fluid high frequencies of CD8+ T cells that are specific for certain viral epitopes 英文参考文献.docVIP
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SpecificityofTcellsinsynovialfluidhighfrequenciesofCD8Tcellsthatarespecificforcertainviralepitopes英文参考文献
/content/2/2/154
Primary research
Specificity of T cells in synovial fluid: high frequencies of CD8+
T cells that are specific for certain viral epitopes
Linda C Tan, Alastair G Mowat*, Chrysoula Fazou, Tim Rostron, Helen Roskell*,
P Rod Dunbar, Claire Tournay?, Fran?ois Romagné?, Marie-Alix Peyrat?,
Elisabeth Houssaint?, Marc Bonneville?, Alan B Rickinson§,
Andrew J McMichael and Margaret FC Callan
John Radcliffe Hospital and *Nuffield Orthopaedic Centre, Oxford, UK, ?Immunotech SA,
Marseilles and ?INSERM U643 Institute Biologie, Nantes, France, and §University of Birmingham,
Birmingham, UK
Received: 1 October 1999
Arthritis Res 2000,2:154–164
Revisions requested: 27 October 1999
Revisions received: 10 November 1999
Accepted: 27 October 1999
The electronic version of this article can be found online at
/content/2/2/154
Published: 7 February 2000
? Current Science Ltd
Statement of findings
CD8+ T cells dominate the lymphocyte population in synovial fluid in chronic inflammatory
arthritis. It is known that these CD8+ T cells are often clonally or oligoclonally expanded, but
their specificity and their relevance to the pathogenesis of joint disease has remained
unclear. We found that as many as 15.5% of synovial CD8+ T cells may be specific for a
single epitope from an Epstein–Barr virus lytic cycle protein. The virus-specific T cells within
the joint showed increased expression of markers of activation and differentiation compared
with those in the periphery, and retained their functional capacity to secrete proinflammatory
cytokines on stimulation. These activated, virus-specific CD8+ T cells could therefore
interact with synoviocytes, either by cell–cell contact or by a cytokine network, and play a
‘bystander’ role in the maintenance of inflammation in patients with arthritis.
Keywords: CD8+ T cell, Epstein–Barr virus lytic cycle, human leucocyte antigen peptide tetrameric complex,
rheumatoid arthritis, viral immunity
Abstra
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