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Research Article Free access | 10.1172/JCI114817

Activation pathways of synovial T lymphocytes. Expression and function of the UM4D4/CDw60 antigen.

D A Fox, J A Millard, L Kan, W S Zeldes, W Davis, J Higgs, F Emmrich, and R W Kinne

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

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Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

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Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

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Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

Find articles by Zeldes, W. in: PubMed | Google Scholar

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

Find articles by Davis, W. in: PubMed | Google Scholar

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

Find articles by Higgs, J. in: PubMed | Google Scholar

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

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Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

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Published October 1, 1990 - More info

Published in Volume 86, Issue 4 on October 1, 1990
J Clin Invest. 1990;86(4):1124–1136. https://doi.org/10.1172/JCI114817.
© 1990 The American Society for Clinical Investigation
Published October 1, 1990 - Version history
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Abstract

Accumulating evidence implicates a central role for synovial T cells in the pathogenesis of rheumatoid arthritis, but the activation pathways that drive proliferation and effector function of these cells are not known. We have recently generated a novel monoclonal antibody against a rheumatoid synovial T cell line that recognizes an antigen termed UM4D4 (CDw60). This antigen is expressed on a minority of peripheral blood T cells, and represents the surface component of a distinct pathway of human T cell activation. The current studies were performed to examine the expression and function of UM4D4 on T cells obtained from synovial fluid and synovial membranes of patients with rheumatoid arthritis and other forms of inflammatory joint disease. The UM4D4 antigen is expressed at high surface density on about three-fourths of synovial fluid T cells and on a small subset of synovial fluid natural killer cells; in synovial tissue it is present on more than 90% of T cells in lymphoid aggregates, and on approximately 50% of T cells in stromal infiltrates In addition, UM4D4 is expressed in synovial tissue on a previously undescribed population of HLA-DR/DP-negative non-T cells with a dendritic morphology. Anti-UM4D4 was co-mitogenic for both RA and non-RA synovial fluid mononuclear cells, and induced IL-2 receptor expression. The UM4D4/CDw60 antigen may represent a functional activation pathway for synovial compartment T cells, which could play an important role in the pathogenesis of inflammatory arthritis.

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