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Infect Immun, March 1998, p. 1092-1099, Vol. 66, No. 3
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Biased T-Cell Antigen Receptor Repertoire in Lyme Arthritis

Karen Roessner,1 Harsh Trivedi,1 Lakshmi Gaur,2 Diantha Howard,3 John Aversa,4 Sheldon M. Cooper,1 Leonard H. Sigal,5 and Ralph C. Budd1,*

Division of Immunobiology1 and Clinical Research Center,3 Department of Medicine, The University of Vermont College of Medicine, Burlington, Vermont 05405; Immunogenetics Laboratory, Puget Sound Blood Center, Seattle, Washington 980272; Department of Orthopedics, Yale University School of Medicine, New Haven, Connecticut 065204; and Division of Rheumatology and Connective Tissue Research, Department of Medicine, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, New Brunswick, New Jersey 089035

Received 24 September 1997/Returned for modification 23 October 1997/Accepted 2 December 1997

A common concern with many autoimmune diseases of unknown etiology is the extent to which tissue T-lymphocyte infiltrates, versus a nonspecific infiltrate, reflect a response to the causative agent. Lyme arthritis can histologically resemble rheumatoid synovitis, particularly the prominent infiltration by T lymphocytes. This has raised speculation about whether Lyme synovitis represents an ongoing response to the causative spirochete, Borrelia burgdorferi, or rather a self-perpetuating autoimmune reaction. In an effort to answer this question, the present study examined the repertoire of infiltrating T cells in synovial fluid from nine Lyme arthritis patients, before and after stimulation with B. burgdorferi. Using a highly sensitive and consistent quantitative PCR technique, a comparison of the T-cell antigen receptor (TCR) beta -chain variable (Vbeta ) repertoires of the peripheral blood and synovial fluid showed a statistically significant increase in expression of Vbeta 2 and Vbeta 6 in the latter. This is remarkably similar to our previous findings in studies of rheumatoid arthritis and to other reports on psoriatic skin lesions. However, stimulation of synovial fluid T cells with B. burgdorferi provoked active proliferation but not a statistically significant increase in expression of any TCR Vbeta , including Vbeta 2 and Vbeta 6. Collectively, the findings suggest that the skewing of the TCR repertoire of fresh synovial fluid in Lyme arthritis may represent more a synovium-tropic or nonspecific inflammatory response, similar to that occurring in rheumatoid arthritis or psoriasis, rather than a specific Borrelia reaction.


* Corresponding author. Mailing address: Division of Immunobiology, Given Medical Building, C-303, The University of Vermont College of Medicine, Burlington, VT 05405-0068. Phone: (802) 656-2286. Fax: (802) 656-3854. E-mail: rbudd{at}zoo.uvm.edu.




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